What Jobs are available for Clinical Trials in Singapore?

Clinical Research Nurse

The successful candidate will be responsible for screening study participants according to regulatory guidelines and ethical standards.

• Conduct informed consent discussions and ensure participants understand the study's requirements.
• Monitor patient progress and collect data during clinical trials, ensuring accurate documentation.
• Administer study-related interventions as per protocol, including medications and treatments.
• Conduct assessments and follow-ups with participants, addressing any concerns and providing education.

Key Responsibilities Include:

• Screening and enrollment of patients in accordance with protocol.
• Collection of data from patients during their participation in studies.
• Monitoring of patients' responses to treatment and collection of relevant data.
• Assessment of patient safety and reporting of any adverse events or reactions.

• Diploma/Degree in Nursing
• Valid SNB & BCLS required
• Able to perform IV Cannulation and Phlebotomy

This role offers a unique opportunity to work on cutting-edge research projects while developing your clinical skills and knowledge.

The role of Senior Contract Specialist involves reviewing and finalizing contracts related to clinical trials. This position requires expertise in negotiating contracts, managing document timelines, supervising team members, and performing administrative tasks with high accuracy.

1. Contract Negotiations: Assist in negotiations with clients and vendors to finalize clinical trial contracts.
2. Document Management: Oversee the preparation, review, and approval of contracts and related documents.
3. Team Supervision: Supervise team members to ensure they meet deadlines and deliver high-quality work.
4. Administrative Tasks: Perform various administrative tasks such as data entry, record-keeping, and reporting.

• Education: A degree in a relevant field such as business, law, or healthcare.
• Experience: At least 6-8 years of experience in contract management, staff supervision, and communication skills are required.
• Skills: Strong negotiation skills, attention to detail, excellent communication skills, and ability to work under pressure.

This role offers an exciting opportunity to work on challenging projects and develop your career in a dynamic environment.

We encourage applications from experienced professionals who can bring their expertise and passion for contract management to this role.

We are seeking a skilled and experienced Research Nurse to join our team.

• Location: West
• Hours: Morning/ Day
• No Overnight Shifts:
• On-the-Job Training: Provided for Research Field

To screen study participants in accordance with regulatory guidelines and ethical standards. To conduct informed consent discussions and ensure participants understand the study's requirements.

To monitor patient progress and collect data during clinical trials, ensuring accurate documentation. To administer study-related interventions as per protocol, including medications and treatments.

To conduct assessments and follow-ups with participants, addressing any concerns and providing education.

• Valid SNB & BCLS required
• Diploma/Degree in Nursing
• Able to perform IV Cannulation and Phlebotomy

Treatment
Healthcare
Phlebotomy
Medication Administration
Administration
Clinical Trials
Protocol
Interventions
Nursing
Accent
IV
Screening
Medical Records
Nursing Care

Interested candidates please send in your resume.

We are looking for a Senior / Manager with sufficient professional experience and skills to fulfill a specialist role that can contribute to the development of the clinical trial program within National Cancer Centre Singapore (NCCS). The role will mainly assist our Clinical Trials Office to review and finalize contracts related to clinical trials for the Division of Clinical Trials & Epidemiological Sciences (CTE).
Main Duties:
Assist to review clinical trial contracts and work closely with the SingHealth Legal Department to negotiate agreement terms with commercial sponsors, CROs, academic institutions or international trial groups.
Assist in checking hard copy contract documents and obtaining signatures from the NCCS's signatories.
Keep track of agreement timelines and chase for replies if a party has not replied for the past two weeks.
Supervise and provide advice to the executives of the Feasibility Team in NDA negotiation and to act as back-up for such review and negotiation during manpower shortage.
Assist in approving online payments in APIMS, training applications in PeopleConnexion (SuccessFactors)and any other online applications assigned.
Help to oversee financial and insurance reporting to CTCC as well as annual NMRC reporting.
Assist in submission and updating of the clinicaltrials.gov, check and approve archiving costs and payment to archiving company and MRO.
File and maintain executed contracts and ensure these are stored securely to maintain confidentiality and prevent loss or damage.
Perform any other duties assigned by the supervisors or the Clinical Trials Office higher management staff
Main Requirements:
A recognised degree, with at least 6 to 8 years of relevant experience in negotiating clinical trial contacts or research study contracts as well as experience in staff supervision.
Preference for individuals with good knowledge of clinical trial conduct procedures.
Well versed in relevant laws and regulations applicable to trial conduct including HBRA, Health Products and Medicines Act, Health Product (Clinical Trial) Regulation, PDPA and ICH GCP.
Strong communication and writing skills, good command of language, good people skills and strong ability to be a good team player.
Strong leadership and management skills.
Meticulous, sharp and driven
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Responsibilities

• Be a part of the operational team in Clinical Trials and Research Unit (CTRU)
• Manages and supervises a team of Clinical Research Coordinators (CRCs) in providing research support to the CGH research community including providing on the job training for junior colleagues, leads and mentors them to ensure smooth and efficient daily operation
• Works closely with Principal Investigator (PI), study team members, sponsor representatives, colleagues, etc to support research initiatives and activities to achieve CGH's research vision
• Supports and provides guidance on the administration and conduct of research projects, to ensure compliance to applicable regulations and policies
• Ensures every study budget is sufficient for its intended purposes, project funds expensed within budget, following proper financial policies/guideline and timely and accurate reimbursement to subjects
• Spearheads complex research projects, develops study specific documents and assists in the overall planning for the conduct of the study
• Prepares and handles study specific audit and/or inspection and initiates internal and external studies quality control activities
• Draft, review and implement department's Standing Operating Procedures (SOPs) and work instructions.  Ensure that these are updated to reflect current practices and regulatory requirements.
• To take on projects as assigned from time to time

Requirements

• Degree in Nursing with valid Singapore Nursing Board (SNB) practicing certificate or Degree in Life Science / Pharmaceutical Science/Clinical Trials Management
• At least 7 years' experience in clinical research activities
• Bilingual and/or proficient in local dialects
• Meticulous and focused
• Able to multi-task with good time management skills
• Good people management skills
• Good team player

Only shortlisted candidates will be notified

Project Officer (Clinical Trials & Translational Research) page is loaded# Project Officer (Clinical Trials & Translational Research)locations:
NTU Main Campus, Singaporetime type:
Full timeposted on:
Posted Todayjob requisition id:
R **Join Our Team at the School of Biological Sciences, Nanyang Technological University, Singapore**The School of Biological Sciences (SBS), part of the College of Science, was established in 2002 with a mission to advance biological and biomedical sciences. At SBS, our research spans various areas, including infectious diseases, immunology, neurodegenerative diseases, telomere biology, and genome function. Over the years, SBS has attracted talented individuals from around the world and Singapore to join as scientific leaders and researchers.For more details, please view are looking for a Project Officer to join the Yang Lab at NTU ( The successful candidate will contribute to an interdisciplinary project evaluating the clinical efficacy and biological mechanisms of traditional, complementary, and integrative medicine (TCIM) interventions for symptom management in cancer populations.The role will focus on coordinating clinical trials and supporting laboratory operations, bridging patient-centered trial activities with bench-based biospecimen handling and multiomics investigations. Through this work, the candidate will be well-positioned to grow at the interface of clinical and laboratory science, while shaping a distinctive academic and professional trajectory.**Key Responsibilities:*** Coordinate randomized clinical trials, including ethics/IRB application and regulatory compliance* Manage trial logistics, patient recruitment, scheduling, and follow-up* Oversee collection, processing, and management of clinical data and biospecimens* Conduct data entry, curation, quality control, and preliminary analyses* Oversee laboratory operations, ensuring compliance with institutional and local safety regulations and good laboratory practices* Manage procurement of equipment, reagents, and consumables* Train and onboard new research staff and students* Liaise with clinical collaborators, institutional partners, and external stakeholders* Support project reporting and documentation for funding and administrative purposes**Job Requirements:*** Bachelor's degree in life sciences, biomedical sciences, public health, social sciences, or related field* At least 1-2 years of relevant experiences in clinical trial coordination, IRB submissions, or patient-facing research (entry-level candidates with strong interest are welcome to apply)* Familiarity with biospecimen collection and handling, molecular biology, or omics techniques* Good written and oral communication skills* Proficiency in data management, statistical analysis, or clinical research sofeware* Strong organizational and project management skills* Excellent interpersonal skills to work both independently and collaboratively within a multidisciplinary team* Demonstrated interest in integrative medicine, oncology, or translational researchThe College of Science seeks a diverse and inclusive workforce and is committed to equality of opportunity. We welcome applications from all and recruit on the basis of merit, regardless of age, race, gender, religion, marital status and family responsibilities, or disability.We regret to inform that only shortlisted candidates will be notified.Hiring Institution: NTUNTU is also home to world-class autonomous institutes – the National Institute of Education, S Rajaratnam School of International Studies, Earth Observatory of Singapore, and Singapore Centre for Environmental Life Sciences Engineering – and various leading research centres such as the Nanyang Environment & Water Research Institute (NEWRI) and Energy Research Institute @ NTU ( ).Ranked amongst the world's top universities by QS, NTU has also been named the world's top young university for the past seven years. The University's main campus is frequently listed among the Top 15 most beautiful university campuses in the world and has 57 Green Mark-certified (equivalent to LEED-certified) buildings, of which 95% are certified Green Mark Platinum. Apart from its main campus, NTU also has a campus in Novena, Singapore's healthcare district.Under the NTU Smart Campus vision, the University harnesses the power of digital technology and tech-enabled solutions to support better learning and living experiences, the discovery of new knowledge, and the sustainability of resources.For more information, visit
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You will be part of the operational team in Clinical Trials & Research Unit (CTRU). You will work alongside members of the project team to provide project management service for projects that fulfil eligibility criteria under oversight of the Project Manager.

Responsibilities:

• Able to lead or facilitate project discussions independently, effectively and efficiently
• Ensure smooth and effective conduct of research projects according to applicable regulations by informed study teams

• To assist Principal Investigators in project organization which includes the following:

• Budget estimate and planning

• Grant(s) application (if applicable)
• Submission to ethics and regulatory bodies, and tracking the approval status
• Sourcing for external vendors/suppliers and assisting in negotiation of acceptable costs
• To manage, guide, supervise and review the performance evaluation of the project team members and review the quality of the work completed by the project team on a regular basis
• To assist in the drafting of relevant project progress reports including the analysis, interpretation and reporting process of findings and results as well as to assist in the preparation of manuscripts, reports and presentation materials (if applicable)
• Assist in the review and implementation of department SOPs and work instructions
• To take on projects as assigned from time to time

Requirements:

• Degree in Life Sciences/ Pharmaceutical Science/ Clinical Trials Management
• At least 4 years relevant experience in clinical project management. Those with advance proficiency in Project Management and expert knowledge of trial procedures, institutional, CIRB & regulatory authority requirements for managing clinical trial would be at an advantage
• Team Player and ability to multi-task, with good time management
• Self-motivated and ability to work in a fast-paced environment
• Good interpersonal relationship skills

Only shortlisted candidates will be notified

The Senior Manager/ Manager assumes responsibility to support Director for all administrative and operational functions of the Clinical Trials and Research Centre (CTRC). He/She is responsible for assisting in supervising and developing the staff at CTRC in providing quality clinical research related services to the hospital, investigators, and sponsors/ clinical research organisations (CRO).

The job responsibilities include:

• Ensure that all trials managed by CTRC are conducted in strict adherence to regulatory, ethical, Good Clinical Practice and protocols.
• Oversee the effective allocation and management of resources to support the execution of trials within CTRC.
• Design and implement a comprehensive training program for CTRC staff to maintain compliance with latest regulations and guidelines and conduct periodic review on staff performance.
• Oversee talent retention and succession planning.
• Building a strong pipeline to meet CTRC manpower needs.
• Provide operational oversight for CTRC's day-to-day activities and ensuring a seamless and effective workflow.
• Oversee and manage the CTRC's budget and ensure accurate financial planning, timely billing, and effective accounts management processes.
• Monitor expenditures to maintain alignment with departmental financial goals.
• Lead quality assurance and quality control initiatives to enhance CTRC's compliance, service quality and competitiveness.
• Develop and monitor CTRC's key performance indicators (KPIs), i.e. study start-up timelines, budget, staff performance etc. for continuous improvement.
• Collaborate with the Director to develop and implement business strategies aimed at expanding the CTRC's reach and impact.
• Build and strengthen partnerships to enhance clinical trials/ clinical research opportunities and drive growth initiatives that align with the CTRC's goals.
• Participate in departmental activities, contribute to institutional initiatives, and fulfil additional duties as required by management

Job Requirements:

• Possess a good general degree, preferably in healthcare related fields.
• Minimum of 8-10 years relevant clinical trial/research work experiences, with at least 4 years in a supervisory/management capacity.
• Possess a strong track record of performance and leadership/ people developer.
• Possess excellent interpersonal, communication, coordination and time management skills.
• Extensive experience in clinical trials operations and management
• Able to work independently and meticulously.
• Effective presentation and organisational skills

Job description

• To closely involved in patient/volunteer recruitment, coordination and follow‐up for clinical studies.
• To liaise and communicate with all team members of the research projects to ensure smooth running of the project.
• To provide administrative and secretarial support to research projects, such as organizing regular meetings to maintain regular communication with other members of the research team and procurement of materials.
• To assist clinical study database formation, data collection.

Interested candidates please send in your resume to:



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