27 Clinical Development jobs in Singapore

We are seeking an exceptional Clinical Development Specialist to join our team.

As a Clinical Development Specialist, you will play a vital role in the development and implementation of clinical programs that enhance patient care and outcomes. Your primary responsibilities will include:

• Clinical Research: Collaborate with cross-functional teams to design, execute, and analyze clinical trials, ensuring compliance with regulatory requirements and industry best practices.
• Quality Assurance: Conduct regular site monitoring visits to ensure adherence to Good Clinical Practice (GCP) guidelines and maintain high-quality data collection.
• Quality Improvement: Analyze data and identify areas for process improvements, implementing changes to optimize clinical trial operations.

To be successful as a Clinical Development Specialist, you must possess:

• A degree in Pharmacy or a related field;
• At least 3 years of experience in clinical research or a related field;
• Strong knowledge of GCP regulations and industry standards;
• Excellent analytical and problem-solving skills;
• Ability to work independently and collaboratively in a fast-paced environment.

As a valued member of our team, you can expect:

• A competitive salary and benefits package;
• Opportunities for professional growth and development;
• A dynamic and supportive work environment.

We are committed to fostering a diverse and inclusive workplace culture. If you are a motivated and detail-oriented individual who is passionate about delivering high-quality clinical services, we encourage you to apply.

About Applied Medical

Applied Medical is a new generation medical device company with a strong global reputation in healthcare. Our proven commitment to innovation has fueled our rapid business growth and expansion for more than 30 years, with a vertically integrated business model enabling our team members to develop technologies that enhance clinical care. We believe in the power of working together to make a meaningful and positive difference and have curated an environment where team members of diverse backgrounds are valued, challenged, and acknowledged.

Position Description

The incumbent will lead the management of the entire product/program life cycle. This includes being a team resource and expert through the various stages of product/program life cycles, including but not limited to research on clinical/customer needs, R&D, sales trials, product launch, post market surveillance, inventory management, and field support. Work closely with the global Clinical Development teams and align on strategies and best practices.

Essential Duties and Responsibilities

• Contribute to the development of strategies and implementation to increase market adoption and penetration of Applied's best solutions.
• Develop expertise of how our devices/programs are used by customers and maintain knowledge of main competition.
• Provide leadership and expertise for any product/program development or enhancement projects, including but not limited to the design input, design validation, hazard analysis, Clinical Data research and compilation, post-market surveillance, complaints, labels & Instructions for Use (IFU) and pricing.
• Forge relationships with thought leaders in their respective markets to enhance understanding of clinical needs.
• Contribute to strategic decision-making for product/program life cycle.
• Manage sales trials or education projects relating to product/program launches or improvements.
• Protect and build product brands, including participation and contribution to organized national and international meetings and congresses.
• Mentor team members and act as a recognized resource to local team.
• Contribute to selection of appropriate team members.
• Assist in other cross-functional and interdepartmental projects that may require support.

Working Relationships

• Clinical Development team functions include mentoring and providing expertise to Clinical Development team members.
• Product/Program related projects may require cooperation with Engineering, Market Implementation, Branding, Regulatory, Education and Field Implementation teams.
• General product/program, competitive analysis and relevant reports should be shared and presented to the global Clinical Development team members.
• Product/program launches and trade shows (domestic and international) will require collaboration with the Education, Branding, Market Implementation, Field Implementation and global Clinical Development teams.
• Pricing changes and obsolescence projects will require cooperation with Senior Management, Clinical Development, Customer Relations, Field Operations, Contracts, international Customer Relations, and international Operations teams.
• Creation and updates to, product support material (PSM) and customer correspondence require collaboration with the Market Implementation and Branding teams.
• Support for Clinical Evaluation and post-market surveillance may require interface with Field Implementation, international and domestic Customer Relations, Regulatory, Field Operations and global Clinical Development teams.

Job Qualifications

Knowledge, Skills & Abilities:

• Excellent written and oral communication skills
• Ability to facilitate collaboration among the team
• Ability to formulate and critically assess reports and present findings
• Ability to execute tasks quickly and with accuracy and consistency
• Ability to facilitate communication amongst cross-functional teams
• Proficiency in using Microsoft Office programs, including but not limited to Word, Excel, PowerPoint, Outlook

Education and/or Formal Training:

• University Graduate
• Basic mathematics and analysis
• Statistics (preferred)

Experience:

• Minimum 3 years of project/product management expertise (medical device industry preferred)
• Experience in giving presentations
• Data mining and analysis (preferred)
• OR experience (preferred)

Working Environment

• The role will be performed in an office environment with needs to be at customers' sites, and/or meeting/congress locations (domestically and internationally).
• Occasional need to travel internationally.

Applied Medical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where Applied Medical operates.

About Applied Medical

Applied Medical is a new generation medical device company with a strong global reputation in healthcare. Our proven commitment to innovation has fueled our rapid business growth and expansion for more than 30 years, with a vertically integrated business model enabling our team members to develop technologies that enhance clinical care. We believe in the power of working together to make a meaningful and positive difference and have curated an environment where team members of diverse backgrounds are valued, challenged, and acknowledged.

Position Description

The incumbent will lead the management of the entire product/program life cycle. This includes being a team resource and expert through the various stages of product/program life cycles, including but not limited to research on clinical/customer needs, R&D, sales trials, product launch, post market surveillance, inventory management, and field support. Work closely with the global Clinical Development teams and align on strategies and best practices.

Essential Duties and Responsibilities

• Contribute to the development of strategies and implementation to increase market adoption and penetration of Applied’s best solutions.
• Develop expertise of how our devices/programs are used by customers and maintain knowledge of main competition.
• Provide leadership and expertise for any product/program development or enhancement projects, including but not limited to the design input, design validation, hazard analysis, Clinical Data research and compilation, post-market surveillance, complaints, labels & Instructions for Use (IFU) and pricing.
• Forge relationships with thought leaders in their respective markets to enhance understanding of clinical needs.
• Contribute to strategic decision-making for product/program life cycle.
• Manage sales trials or education projects relating to product/program launches or improvements.
• Protect and build product brands, including participation and contribution to organized national and international meetings and congresses.
• Mentor team members and act as a recognized resource to local team.
• Contribute to selection of appropriate team members.
• Assist in other cross-functional and interdepartmental projects that may require support.

Working Relationships

• Clinical Development team functions include mentoring and providing expertise to Clinical Development team members.
• Product/Program related projects may require cooperation with Engineering, Market Implementation, Branding, Regulatory, Education and Field Implementation teams.
• General product/program, competitive analysis and relevant reports should be shared and presented to the global Clinical Development team members.
• Product/program launches and trade shows (domestic and international) will require collaboration with the Education, Branding, Market Implementation, Field Implementation and global Clinical Development teams.
• Pricing changes and obsolescence projects will require cooperation with Senior Management, Clinical Development, Customer Relations, Field Operations, Contracts, international Customer Relations, and international Operations teams.
• Creation and updates to, product support material (PSM) and customer correspondence require collaboration with the Market Implementation and Branding teams.
• Support for Clinical Evaluation and post-market surveillance may require interface with Field Implementation, international and domestic Customer Relations, Regulatory, Field Operations and global Clinical Development teams.

Job Qualifications

Knowledge, Skills & Abilities:

• Excellent written and oral communication skills
• Ability to facilitate collaboration among the team
• Ability to formulate and critically assess reports and present findings
• Ability to execute tasks quickly and with accuracy and consistency
• Ability to facilitate communication amongst cross-functional teams
• Proficiency in using Microsoft Office programs, including but not limited to Word, Excel, PowerPoint, Outlook

Education and/or Formal Training:

• University Graduate
• Basic mathematics and analysis
• Statistics (preferred)

Experience:

• Minimum 3 years of project/product management expertise (medical device industry preferred)
• Experience in giving presentations
• Data mining and analysis (preferred)
• OR experience (preferred)

Working Environment

• The role will be performed in an office environment with needs to be at customers’ sites, and/or meeting/congress locations (domestically and internationally).
Occasional need to travel internationally

Applied Medical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where Applied Medical operates.

Clinical Service Planning Role

We are seeking a skilled Clinical Service Planner to support the development and implementation of clinical service plans for hospitals. This role involves close collaboration with clinical leads, medical/surgical division leads, and other stakeholders to ensure that plans are comprehensive, effective, and aligned with hospital goals.

Key Responsibilities:

• Support the development and implementation of clinical service plans for hospitals.
• Collaborate with clinical leads, medical/surgical division leads, and other stakeholders to ensure alignment and effectiveness.
• Contribute to the creation of comprehensive plans that meet hospital goals.

Requirements:

• Bachelor's degree in a relevant field such as healthcare administration or management.
• At least 3 years of experience in clinical service planning or a related field.
• Strong analytical and problem-solving skills.
• Effective communication and collaboration skills.

Benefits:

• Opportunity to work in a dynamic and growing industry.
• Collaborative and supportive team environment.
• Promotion opportunities based on performance.

We are seeking a highly skilled and innovative Scientist to join our R&D Lab.

The ideal candidate will be passionate about biologic drug development, have expertise in designing and developing assays, and demonstrate exceptional leadership skills.

• Design, develop, validate, and perform bioassays compliant with FDA/EMA, OECD GLP principles and other regulatory guidelines.
• Data compilation, interpretation, and statistical analysis when required.
• Perform studies/assays and ensure data integrity.
• Draft, revise, and review study protocols, study reports, and SOPs.
• Review various types of documents, data, and provide scientific input.
• Delegate scientific tasks to team members and ensure timelines are met.
• Perform literature reviews and provide technical and scientific expertise as required.

• PhD in biomedical science, life science, or equivalent.
• Proficiency in mammalian cell culture and aseptic techniques.
• Experience in cell-based assays, ligand binding assays, such as ELISA and BLI, and microscopy techniques.
• Knowledge in SDS-PAGE, Western Blot, flow cytometry, and immunostaining is desirable.
• Experience in drafting study protocols, study reports, and SOPs.
• Experience in method development, method validation, biologic drug characterization, and PK & immunogenicity analysis.
• Proficiency with LIMS, office management software (MS Office, Teams), and statistical tools (Prism, SPSS, or PLA).
• Experience in GLP/GCLP and/or ISO17025 is a plus.
• Ability to deliver quality data on time to meet project timelines.
• Outstanding organizational, interpersonal, and oral communication skills are critical.
• Superior attention to detail, problem-solving, and troubleshooting skills are desirable.

Job Scope:

• Manage investigational products, controlled drugs, and therapeutic products – including sourcing, receiving, storage, labelling, dispensing, reconciliation, and documentation
• Perform extemporaneous preparations, aseptic compounding, and related dispensing duties
• Maintain pharmacy operations including inventory management, cleanliness, and environmental monitoring
• Ensure proper management of randomization and unblinding procedures for blinded clinical trials
• Oversee handling and maintenance of pharmacy equipment
• Support cross-functional operations and ad-hoc duties as required

Requirement:

• Singapore-Registered Pharmacist
• Experience in compounding, cleanroom, or manufacturing setting will be good

Interested candidates, please forward your resume to

Consultant: Huang Jingsheng Kevyn (R13338)

Recruit Express Pte Ltd (99C4599)

This is an exciting opportunity for a Freelance Clinical Trial Nurse to join our research team. As a key member of our team, you will play a vital role in ensuring the success of clinical trials.

• Assist the research team in various tasks related to clinical trials.
• Ensure the smooth execution of trial procedures and protocols.
• Maintain accurate and detailed records of trial progress.

Required Skills and Qualifications:

We are looking for individuals with the following skills and qualifications:

• Strong knowledge of clinical trial procedures and protocols.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.

Benefits:

As a Freelance Clinical Trial Nurse, you will have the opportunity to work on a variety of projects and develop your skills and expertise. You will also have access to ongoing training and professional development opportunities.

Other Opportunities:

Working as a Freelance Clinical Trial Nurse offers many opportunities for career advancement and personal growth. You will have the chance to work with a dynamic team and contribute to the success of clinical trials.

This is a full-time contract position with 5.5 days of office hours per week.

We are looking for a highly motivated and organized individual with a passion for clinical research to join our team as a Research Coordinator.

The selected candidate will be responsible for coordinating studies, managing budgets, and working closely with the Principal Investigator (PI) to achieve project goals.

The ideal candidate will have strong interpersonal skills, experience in clinical research, and knowledge of healthcare administration.

We offer a dynamic and supportive work environment with opportunities for professional growth and development.

The successful candidate will have opportunities for career growth and personal development.

• Coordinate with the team and clinics to set up study sites, including making logistics arrangements and preparing for studies and meetings.
• Manage study budget, tracking expenses, and making financial payments.
• Coordinate studies across multiple sites and collaborate with other teams as needed.
• Monitor study progress and coordinate regular reviews with the study team.
• Assist in preparing study-related presentations and materials.
• Evaluate research results and provide feedback.

• Possess a relevant Diploma or Degree.

• This role is ideal for individuals with a strong understanding of research protocols.
• We are looking for a motivated individual who is passionate about clinical trials.

Job Summary

   We are seeking a skilled Clinical Research Pharmacist to join our team. In this role, you will be responsible for ensuring the proper management of Investigational Product Controlled Drug Therapeutic Product.

   Key Responsibilities:

• Source, receive, store, prepare, dispense, label, and inventory manage Investigational Products.

• Perform extemporaneous preparation, aseptic compounding, and other dispensing activities as required.

• Manage pharmacy operational activities, including inventory control, maintaining cleanliness of pharmacy areas, and environmental monitoring.

• Ensure compliance with regulations regarding randomization and unblinding procedures for clinical trials.

• Maintain equipment in the pharmacy and perform cross-functional duties as needed.

Qualification Requirements

• Registered Pharmacist license in Singapore.

• Experience in compounding or working in a cleanroom or manufacturing setting is preferred.