782 Clinical Trial jobs in Singapore

Roles & Responsibilities

About TUMCREATE

TUMCREATE is a multidisciplinary research platform of the Technical University Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies.

The LightSPAN project is funded by the National Research Foundation of Singapore and aims to investigate how we can optimize light exposure to support health and well-being across the lifespan, with a specific focus on optimizing light exposure in seniors.

Please visit for more information about TUMCREATE.

Job Purpose/Objective of the Position:

• Join our mission to revolutionize healthy ageing The LightSPAN Project at TUMCREATE is seeking a passionate, people-focused Research Assistants to help us run an ambitious research-focused groundbreaking clinical trial improving seniors' health through optimized light exposure and contribute to scientific discoveries in collaboration with Lion Befrienders.
• We value diversity and welcome applicants from all backgrounds who are passionate about making a difference in seniors' health.

Time commitment:

• We require part- and/or full- time students and recent University or Polytechnic graduates from October 2025 to April 2026.
• Part-time: you should be able to work at least 8 hours per week. We pay an allowance of SGD 15 per hour.
• Full-time: Starting salary SGD 2200.

Job responsibilities:

• Recruit and schedule participants, ensuring a positive and professional experience. You will make conduct support calls with participants and station on-site at any Lion Befrienders' branches to recruit senior participants. You will also support the participants to complete our survey forms, explain how to download/use our app and entering data into our database and any other duties. Coaching and transport reimbursement by MRT and buses will be provided.
• Provide warm, supportive interactions with seniors, building trust and engagement
• Collect high-quality research data that will directly inform new health interventions

Job requirements/competencies:

• Background in Nursing, Medicine, Health Sciences, Psychology, Gerontology, Arts, Humanities and Social Sciences, or related fields
• Able to speak local languages to reach out to seniors from different cultures and background
• Empathetic, outgoing, and confident in interacting with seniors
• Detail-oriented, motivated, and able to work independently while contributing to a team
• Problem-solver who can adapt to challenges in a dynamic research environment

What we offer you:

• Opportunity to gain hands-on experience in clinical research and digital health interventions in a cutting-edge internationally oriented team.
• Mentorship from leading experts in ageing and health technology.
• Being part of an international research network
• Joining a vibrant, modern and positive working environment

Applications:

Please send your cover letter (compulsory) detailing your motivation, clearly indicate whether you wish to work part- or full- time or both, and prior expertise, and your CV (max. 2 pages) to

Tell employers what skills you have

Machine Learning
Psychology
Clinical Research
Medicine
Gerontology
Social Sciences
Mentorship
Interventions
Administrative Support
Nursing
Wellbeing
GCP
Health Sciences
Able To Work Independently
Clinical Monitoring

About TUMCREATE
TUMCREATE is a multidisciplinary research platform of the Technical University Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies.
The LightSPAN project is funded by the National Research Foundation of Singapore and aims to investigate how we can optimize light exposure to support health and well-being across the lifespan, with a specific focus on optimizing light exposure in seniors.
Please visit for more information about TUMCREATE.
Job Purpose/Objective of the Position:

• Join our mission to revolutionize healthy ageing The LightSPAN Project at TUMCREATE is seeking a passionate, people-focused Research Assistants to help us run an ambitious research-focused groundbreaking clinical trial improving seniors' health through optimized light exposure and contribute to scientific discoveries in collaboration with Lion Befrienders.
• We value diversity and welcome applicants from all backgrounds who are passionate about making a difference in seniors' health.

Time commitment:

• We require part- and/or full- time students and recent University or Polytechnic graduates from October 2025 to April 2026.
• Part-time: you should be able to work at least 8 hours per week. We pay an allowance of SGD 15 per hour.
• Full-time: Starting salary SGD 2200.

Job responsibilities:

• Recruit and schedule participants, ensuring a positive and professional experience. You will make conduct support calls with participants and station on-site at any Lion Befrienders' branches to recruit senior participants. You will also support the participants to complete our survey forms, explain how to download/use our app and entering data into our database and any other duties. Coaching and transport reimbursement by MRT and buses will be provided.
• Provide warm, supportive interactions with seniors, building trust and engagement
• Collect high-quality research data that will directly inform new health interventions

Job requirements/competencies:

• Background in Nursing, Medicine, Health Sciences, Psychology, Gerontology, Arts, Humanities and Social Sciences, or related fields
• Able to speak local languages to reach out to seniors from different cultures and background
• Empathetic, outgoing, and confident in interacting with seniors
• Detail-oriented, motivated, and able to work independently while contributing to a team
• Problem-solver who can adapt to challenges in a dynamic research environment

What we offer you:

• Opportunity to gain hands-on experience in clinical research and digital health interventions in a cutting-edge internationally oriented team.
• Mentorship from leading experts in ageing and health technology.
• Being part of an international research network
• Joining a vibrant, modern and positive working environment

Applications:
Please send your cover letter (compulsory) detailing your motivation, clearly indicate whether you wish to work part- or full- time or both, and prior expertise, and your CV (max. 2 pages) to .

About TUMCREATE

TUMCREATE is a multidisciplinary research platform of the Technical University Munich (TUM) at the Singapore Campus for Research Excellence and Technological Enterprise (CREATE). We are joining forces with universities, public agencies, and industry for the advancement of future technologies.

The LightSPAN project is funded by the National Research Foundation of Singapore and aims to investigate how we can optimize light exposure to support health and well-being across the lifespan, with a specific focus on optimizing light exposure in seniors.

Please visit for more information about TUMCREATE.

Job Purpose/Objective of the Position:

• Join our mission to revolutionize healthy ageing! The LightSPAN Project at TUMCREATE is seeking a passionate, people-focused Research Assistants to help us run an ambitious research-focused groundbreaking clinical trial improving seniors’ health through optimized light exposure and contribute to scientific discoveries in collaboration with Lion Befrienders.
• We value diversity and welcome applicants from all backgrounds who are passionate about making a difference in seniors’ health.

Time commitment:

• We require part- and/or full- time students and recent University or Polytechnic graduates from October 2025 to April 2026.
• Part-time: you should be able to work at least 8 hours per week. We pay an allowance of SGD 15 per hour.
• Full-time: Starting salary SGD 2200.

Job responsibilities:

• Recruit and schedule participants, ensuring a positive and professional experience. You will make conduct support calls with participants and station on-site at any Lion Befrienders’ branches to recruit senior participants. You will also support the participants to complete our survey forms, explain how to download/use our app and entering data into our database and any other duties. Coaching and transport reimbursement by MRT and buses will be provided.
• Provide warm, supportive interactions with seniors, building trust and engagement
• Collect high-quality research data that will directly inform new health interventions

Job requirements/competencies:

• Background in Nursing, Medicine, Health Sciences, Psychology, Gerontology, Arts, Humanities and Social Sciences, or related fields
• Able to speak local languages to reach out to seniors from different cultures and background
• Empathetic, outgoing, and confident in interacting with seniors
• Detail-oriented, motivated, and able to work independently while contributing to a team
• Problem-solver who can adapt to challenges in a dynamic research environment

What we offer you:

• Opportunity to gain hands-on experience in clinical research and digital health interventions in a cutting-edge internationally oriented team.
• Mentorship from leading experts in ageing and health technology.
• Being part of an international research network
• Joining a vibrant, modern and positive working environment

Applications:

Please send your cover letter (compulsory) detailing your motivation, clearly indicate whether you wish to work part- or full- time or both, and prior expertise, and your CV (max. 2 pages) to .

Job Overview
Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers

Essential Functions

• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.

• May be responsible for delivery and management of smaller, less complex, regional studies.

• Develop integrated study management plans with the core project team.

• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.

• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.

• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.

• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.

• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.

• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.

• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;

• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;

• Ensure the financial success of the project.

• Forecast and identify opportunities to accelerate activities to bring revenue forward.

• Identify changes in scope and manage change control process as necessary.

• Identify lessons learned and implement best practices. May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;

• Adopt corporate initiatives and changes and serve as a change advocate when necessary.

• Provide input to line managers of their project team members’ performance relative to project tasks.

• Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;

Qualifications

• Bachelor's Degree Life sciences or related field

• 6 years of prior relevant experience including > 2 years project management experience or equivalent combination of education, training and experience.

• Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.

• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;

• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.

• Problem solving - Strong problem solving skills.

• Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.

• Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.

• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.

• Prioritisation - Ability to handle conflicting priorities.

• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.

• Quality - Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.

• IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.

• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.

• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.

• Finances - Good understanding of project financials including experience managing, contractual obligations and implications.

• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

#J-18808-Ljbffr

Key Accountabilities:

Trial Preparation

• Accountable for the trial activities for responsible R/OPU, including but not limited to;
• Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities.
• Creation, management and review of the R/OPU trial budget to verify appropriate level of financial oversight and planning accuracy. Timely budget updates based on trial changes.
• Appropriate trial-specific training of R/OPU internal and external partners is performed in line with trial training plan.
• Accurate planning and co-ordination of operational feasibility of trial timelines for their R/OPU; and oversight of trial preparation to verify trial team members are aligned and on track.
• Verifies and provides input into the country and site level feasibility and OPU commitment. Finalize and validate site selection using available data sources and local insights/expertise, in collaboration with other functions.
• Development and implementation of country level engagement plans, recruitment planning and risk mitigation. Co-ordinates development of country level patient facing documents in close collaboration with relevant internal and external stakeholders. Reports patient and site level feedback as strategic insight to contribute to improving trial design with a focus on patient value.
• Frontloading of activities where possible at the R/OPU level to facilitate efficiencies as well as to verify and leverage speed.
• Oversees outsourcing of vendor services in the R/OPU in accordance to operating models and governance.
• Verify timely responses to questions from Regulatory Authority/Ethic Committee and other external stakeholders

Trial Conduct

• Maintains oversights during clinical trial conduct including adherence to GCP and all global and local regulatory requirements; compliance with SOPs and continuous risk monitoring /mitigation. In collaboration with other functions, verifies budget oversight, including support of regular clinical quality monitoring, and safety reporting.
• Monitor progress of patient recruitment endpoints and proactively update and action contingencies throughout trial conduct.
• Support CTL during investigator meetings
• Establish and maintain relationships with external experts, investigational sites, patient organizations and other stakeholders by coordinating and ensuring cross-functional collaboration amongst Clinical Development & Operations (CD&O) ad appropriate functions.
• Active participation in the CD&O community with a special focus on participating in the CTM network, to actively contribute to functional excellence.

Trial Closeout and Reporting

• Verifies timely cleaning and delivery of clinical trial data.
• Responsible for timely, complete and compliant archiving of all relevant R/OPU documents in the TMF, including all required documents from vendors.
• Verifies timely submission of the Clinical Trial Report (CTR) to Regulatory authority/Ethics Committee and other external stakeholders as required by local regulations
• Shares information on trial results with Investigational sites and, if applicable, patients

General Accountabilities

• Build and maintain engagement with Investigators, other site staff and patient organizations (POs), in collaboration with other functions, to verify trial speed and effective start up, conduct and close out.
• Establish and maintain relationships with external experts, investigational sites, patient organizations and other stakeholders by coordinating and ensuring cross-functional collaboration amongst CD&O and appropriate functions.
• Supports CTL to verify issues are raised to Evidence team for timely action or mitigation

Leadership competencies

• Creates an environment that inspires, motivates, and empowers colleagues and promotes one common Clinical Development and Operations (CD&O) identity, contributing to acceleration of clinical development timelines and value creation for patients.
• Fosters a learning culture in CD&O regions by encouraging continuous learning, sharing best practices, and learning from failures
• Embraces innovative technologies, as well as creates and maintains a culture that drives empowerment, smart risk taking and one common CD&O identity.

Compliance with Parexel standards

• Comply with required training curriculum
• Complete timesheets accurately as required
• Submit expense reports as required
• Update CV as required
• Maintain a working knowledge of and comply with Parexel processes, ICHGCPs and other applicable requirements

Skills :

• Strong clinical trial project management experience. In-depth understanding of project management with emphasis on team work to promote high-performance teams
• Experience in Therapeutic Areas relevant in client pipeline is desirable
• Understanding of local/regional major regulations
• Familiarity with guidelines and standard of care is desirable
• Experienced in working with CROs and POs is desirable
• Ability to build and maintain strong relationships of mutual value
• Excellent influencing and communication skills

Knowledge and Experience:

• Strong Communication Skills: Demonstrates AAI approach and skills in complex cross- functional matrix structures of the trial and extended team. Articulates and aligns business strategy/plan on an ongoing basis, ensuring alignment between words and action. Demonstrates active listening skills and cultural awareness.
• Scientific and Operational Expertise: Demonstrates scientific and therapeutic knowledge and operational expertise across all aspects of clinical trial planning and execution. Dimensions of trial complexity include protocol, patients, sites, countries, vendors.
• Leadership and Influence: Demonstrates skills and capabilities in addressing complex situations, confidently setting direction for teams. Demonstrates leadership behaviours of supporting, connecting and empowering teams, providing future direction, demonstrating visionary and innovative thinking and inspiring teams to achieve a common goal. Executes activities with a clear aim to deliver value to patients.
• Strategic Mindset: Strategic and visionary thinker who is future focused, creative, courageous and able to navigate through ambiguity. Integrates study strategy with overall TA portfolio. Embraces cross functional initiatives, applying innovative learnings. Is results-oriented with a global mindset using analytical thinking to provide risk-balanced solutions.
• Coordination and Oversight: Collaborative leader who demonstrates skills and capabilities in setting priorities, managing pace of activities, and efficient usage of resources.
• Project Management: Plans effectively, setting priorities, and defining actions. Makes effective use of resources, and proactively strives for transparency and clarity to accomplish the business deliverables. Translates complex situations to actionable parts. Anticipates and resolves challenges and translates learnings to new projects. Takes smart risks.

Education :

• University degree (e.g. Masters degree or comparable degree), with several years relevant experience in required area, major f

#LI-REMOTE #J-18808-Ljbffr

Job Overview
Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers

Essential Functions

• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.

• May be responsible for delivery and management of smaller, less complex, regional studies.

• Develop integrated study management plans with the core project team.

• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.

• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.

• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.

• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.

• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.

• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.

• May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;

• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;

• Ensure the financial success of the project.

• Forecast and identify opportunities to accelerate activities to bring revenue forward.

• Identify changes in scope and manage change control process as necessary.

• Identify lessons learned and implement best practices. May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;

• Adopt corporate initiatives and changes and serve as a change advocate when necessary.

• Provide input to line managers of their project team members’ performance relative to project tasks.

• Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;

Qualifications

• Bachelor's Degree Life sciences or related field

• 6 years of prior relevant experience including > 2 years project management experience or equivalent combination of education, training and experience.

• Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.

• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;

• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.

• Problem solving - Strong problem solving skills.

• Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.

• Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.

• Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.

• Prioritisation - Ability to handle conflicting priorities.

• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.

• Quality - Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.

• IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.

• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.

• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.

• Finances - Good understanding of project financials including experience managing, contractual obligations and implications.

• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at

#J-18808-Ljbffr

Join to apply for the Clinical Trial Manager role at Medpace

Join to apply for the Clinical Trial Manager role at Medpace

Get AI-powered advice on this job and more exclusive features.

Medpace is currently looking for an experienced Clinical Trial Manager (CTM) to lead global clinical research studies. Medpace is a scientifically led organization offering full-service solutions for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. The Clinical Trial Manager position is the lead role for multiservice global/regional clinical trials. The CTM interacts with sponsors and sites and manages the timeline and project deliverables (minus finance). This role coordinates all services contracted for the study, leading the cross functional team thru all life cycles of the project (from startup to database lock and closure). CTM will attend bid defense meetings and support business development activities, as needed. This position is fully office based in our Singapore office.

Responsibilities

• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
• Serve as primary Sponsor contact for project-specific issues and study deliverables
• Maintain in depth knowledge of protocol, therapeutic area, and indication
• Provide cross-functional oversight of project team members and deliverables, which includes ensuring all necessary project-specific training is provided
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
• Develop operational project plans
• Manage risk assessment and mitigations
• Manage study vendors
• Manage site quality, including direct supervision of project Clinical Research Associates (CRA) and monitoring deliverables
  
  

Qualifications

• Bachelor’s degree or above in health/life science related field;
• At least two years of clinical trial management experience in the Asia Pacific region; indications of interest a plus
• Prior CRO experience is preferred
• Excellent communication skills including good verbal and written English; and
• Flexible, accountable, and comfortable working in a global environment.
  
  

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
  
  

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
  
  

What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Seniority level

• Seniority level Not Applicable

Employment type

• Employment type Full-time

Job function

• Job function Research, Analyst, and Information Technology
• Industries Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Medpace by 2x

Get notified about new Clinical Trial Manager jobs in Singapore, Singapore .

Associate Clinical Trial Manager - PhD / Post-Doc - Infectious Disease Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) Asst Manager/Manager, Clinical Research & Innovation Office Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM)) Associate Clinical Trial Manager - PhD / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (CVRM)) Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology)

Queenstown, Central Singapore Community Development Council, Singapore 1 month ago

Associate Clinical Research Coordinator / Clinical Research Coordinator Associate Clinical Research Coordinator, HORG (1 Year Contract) Research Associate (Clinical Healthy Longevity Trials)

Queenstown, Central Singapore Community Development Council, Singapore 2 months ago

Clinical Research Associate / Senior Clinical Research Associate Clinical Research Associate / Senior Clinical Research Associate Senior Lead Clinical Research Associate, Research Compliance Management Project Coordinator (Senior Executive/ Asst Manager), Clinical Service Planning

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

#J-18808-Ljbffr

**Key Accountabilities:**
Trial Preparation
+ Accountable for the trial activities for responsible R/OPU, including but not limited to;
+ Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities.
+ Creation, management and review of the R/OPU trial budget to verify appropriate level of financial oversight and planning accuracy. Timely budget updates based on trial changes.
+ Appropriate trial-specific training of R/OPU internal and external partners is performed in line with trial training plan.
+ Accurate planning and co-ordination of operational feasibility of trial timelines for their R/OPU; and oversight of trial preparation to verify trial team members are aligned and on track.
+ Verifies and provides input into the country and site level feasibility and OPU commitment. Finalize and validate site selection using available data sources and local insights/expertise, in collaboration with other functions.
+ Development and implementation of country level engagement plans, recruitment planning and risk mitigation. Co-ordinates development of country level patient facing documents in close collaboration with relevant internal and external stakeholders. Reports patient and site level feedback as strategic insight to contribute to improving trial design with a focus on patient value.
+ Frontloading of activities where possible at the R/OPU level to facilitate efficiencies as well as to verify and leverage speed.
+ Oversees outsourcing of vendor services in the R/OPU in accordance to operating models and governance.
+ Verify timely responses to questions from Regulatory Authority/Ethic Committee and other external stakeholders
Trial Conduct
+ Maintains oversights during clinical trial conduct including adherence to GCP and all global and local regulatory requirements; compliance with SOPs and continuous risk monitoring /mitigation. In collaboration with other functions, verifies budget oversight, including support of regular clinical quality monitoring, and safety reporting.
+ Monitor progress of patient recruitment endpoints and proactively update and action contingencies throughout trial conduct.
+ Support CTL during investigator meetings
+ Establish and maintain relationships with external experts, investigational sites, patient organizations and other stakeholders by coordinating and ensuring cross-functional collaboration amongst Clinical Development & Operations (CD&O) ad appropriate functions.
+ Active participation in the CD&O community with a special focus on participating in the CTM network, to actively contribute to functional excellence.
Trial Closeout and Reporting
+ Verifies timely cleaning and delivery of clinical trial data.
+ Responsible for timely, complete and compliant archiving of all relevant R/OPU documents in the TMF, including all required documents from vendors.
+ Verifies timely submission of the Clinical Trial Report (CTR) to Regulatory authority/Ethics Committee and other external stakeholders as required by local regulations
+ Shares information on trial results with Investigational sites and, if applicable, patients
General Accountabilities
+ Build and maintain engagement with Investigators, other site staff and patient organizations (POs), in collaboration with other functions, to verify trial speed and effective start up, conduct and close out.
+ Establish and maintain relationships with external experts, investigational sites, patient organizations and other stakeholders by coordinating and ensuring cross-functional collaboration amongst CD&O and appropriate functions.
+ Supports CTL to verify issues are raised to Evidence team for timely action or mitigation
Leadership competencies
+ Creates an environment that inspires, motivates, and empowers colleagues and promotes one common Clinical Development and Operations (CD&O) identity, contributing to acceleration of clinical development timelines and value creation for patients.
+ Fosters a learning culture in CD&O regions by encouraging continuous learning, sharing best practices, and learning from failures
+ Embraces innovative technologies, as well as creates and maintains a culture that drives empowerment, smart risk taking and one common CD&O identity.
Compliance with Parexel standards
+ Comply with required training curriculum
+ Complete timesheets accurately as required
+ Submit expense reports as required
+ Update CV as required
+ Maintain a working knowledge of and comply with Parexel processes, ICHGCPs and other applicable requirements
**Skills** :
+ Strong clinical trial project management experience. In-depth understanding of project management with emphasis on team work to promote high-performance teams
+ Experience in Therapeutic Areas relevant in client pipeline is desirable
+ Understanding of local/regional major regulations
+ Familiarity with guidelines and standard of care is desirable
+ Experienced in working with CROs and POs is desirable
+ Ability to build and maintain strong relationships of mutual value
+ Excellent influencing and communication skills
**Knowledge and Experience:**
+ Strong Communication Skills: Demonstrates AAI approach and skills in complex cross- functional matrix structures of the trial and extended team. Articulates and aligns business strategy/plan on an ongoing basis, ensuring alignment between words and action. Demonstrates active listening skills and cultural awareness.
+ Scientific and Operational Expertise: Demonstrates scientific and therapeutic knowledge and operational expertise across all aspects of clinical trial planning and execution. Dimensions of trial complexity include protocol, patients, sites, countries, vendors.
+ Leadership and Influence: Demonstrates skills and capabilities in addressing complex situations, confidently setting direction for teams. Demonstrates leadership behaviours of supporting, connecting and empowering teams, providing future direction, demonstrating visionary and innovative thinking and inspiring teams to achieve a common goal. Executes activities with a clear aim to deliver value to patients.
+ Strategic Mindset: Strategic and visionary thinker who is future focused, creative, courageous and able to navigate through ambiguity. Integrates study strategy with overall TA portfolio. Embraces cross functional initiatives, applying innovative learnings. Is results-oriented with a global mindset using analytical thinking to provide risk-balanced solutions.
+ Coordination and Oversight: Collaborative leader who demonstrates skills and capabilities in setting priorities, managing pace of activities, and efficient usage of resources.
+ Project Management: Plans effectively, setting priorities, and defining actions. Makes effective use of resources, and proactively strives for transparency and clarity to accomplish the business deliverables. Translates complex situations to actionable parts. Anticipates and resolves challenges and translates learnings to new projects. Takes smart risks.
**Education** :
+ University degree (e.g. Masters degree or comparable degree), with several years relevant experience in required area, major f
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

**Job Overview**
Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customers
**Essential Functions**
+ Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
+ May be responsible for delivery and management of smaller, less complex, regional studies.
+ Develop integrated study management plans with the core project team.
+ Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
+ Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
+ Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
+ Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.
+ Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
+ Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.
+ May serve as primary or backup project contact with customer and would then own the relationship with the project's key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;
+ Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;
+ Ensure the financial success of the project.
+ Forecast and identify opportunities to accelerate activities to bring revenue forward.
+ Identify changes in scope and manage change control process as necessary.
+ Identify lessons learned and implement best practices. May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;
+ Adopt corporate initiatives and changes and serve as a change advocate when necessary.
+ Provide input to line managers of their project team members' performance relative to project tasks.
+ Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;
**Qualifications**
+ Bachelor's Degree Life sciences or related field
+ 6 years of prior relevant experience including > 2 years project management experience or equivalent combination of education, training and experience.
+ Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.
+ Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;
+ Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.
+ Problem solving - Strong problem solving skills.
+ Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently.
+ Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
+ Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
+ Prioritisation - Ability to handle conflicting priorities.
+ Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
+ Quality - Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.
+ IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
+ Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.
+ Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.
+ Finances - Good understanding of project financials including experience managing, contractual obligations and implications.
+ IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled