331 Clinical Trials jobs in Singapore

We are seeking a highly organized Clinical Study Coordinator to support our team in managing clinical trials.

Key Responsibilities:

• Maintain accurate and up-to-date study files and documents in both physical and electronic formats.
• Assist with preparing study-related materials and training documents, ensuring timely delivery of high-quality results.
• Verify and track clinical trial data to ensure accuracy and completeness, identifying potential issues and proposing solutions.
• Prepare and organize documents for study reviews and monitoring visits, facilitating effective communication among team members.
• Coordinate with the study team, vendors, and clinical staff to ensure seamless execution of clinical trials.
• Receive and register clinical trial participants, adhering to strict protocols and guidelines.
• Process and prepare biological samples for testing and shipment, maintaining accurate records and logs.
• Manage inventory of study supplies and laboratory consumables, minimizing waste and optimizing resource allocation.
• Contribute to the maintenance and documentation of biomedical equipment and laboratory conditions, ensuring compliance with regulatory standards.

Requirements:

• Minimum GCE O Level and above
• Proficient in basic computer applications, particularly Microsoft Office

Attractive remuneration package includes competitive salary and benefits. We value diversity and encourage applicants from all backgrounds to apply. Please note that only shortlisted candidates will be notified.

The role of a Clinical Research Associate is multifaceted and involves providing research support services for clinical trials. As a key member of the Respiratory & CCM team, you will work closely with the Principal Investigator (PI) to ensure the successful execution of clinical studies.

Main responsibilities include:

• Screening patients for eligibility and enrollment into clinical trials.
• Organizing patient visits and ensuring procedures are carried out as per protocol.
• Collecting data and completing clinical reports in a timely manner.
• Recording and reporting adverse events in accordance with Good Clinical Practice guidelines.
• Maintaining accurate site files and records.
• Collaborating with the sponsor company and investigators to provide ancillary services.

Job requirements:

• A bachelor's degree in Science, Health Science, Nursing, or a related field.
• Proficiency in computer applications like Microsoft Access, Excel, PowerPoint, and SPSS.
• Excellent coordination and organizational skills with a strong ability to multitask.
• A certificate in Basic Good Clinical Practice (GCP) or registered nurse with SNB certification is advantageous.

The Clinical Trials Manager is responsible for leading cross-functional teams to deliver global clinical trials. This involves collaborating with sponsors, managing timelines and project deliverables, and coordinating services contracted for the study.

• Project lead role for multiservice global clinical trials
• Interacting with sponsors and managing timeline and project deliverables
• Coordinating all services contracted for the study

• Bachelor's degree in a health-related field;
• At least two years of clinical trial management experience in Asia Pacific region ideally in a CRO environment;
• Experience in Infectious Disease/Ophthalmology/Neurology studies preferred;
• Excellent communication skills including good written and spoken English;
• Flexible, accountable, and comfortable working in a global environment.

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.

Job Opportunity

We are seeking an individual to perform label printing and secondary packaging operational processes for pharmaceutical products in clinical trials.

This role requires strong attention to detail, with a focus on accurate GMP label printing, inspection, over-labelling and secondary packaging activities. The successful candidate will maintain site cleanliness and adhere to standard operating procedures (SOPs) and policies, ensuring all documentation is completed accurately and on time.

Key Responsibilities:

• Ensure accurate GMP label printing, inspection, over-labelling and secondary packaging activities
• Maintain site cleanliness and adheres to standard operating procedures (SOPs) and policies
• Complete all documentation accurately and on time

• Pharmaceutical industry experience
• Maritime logistics knowledge
• Inbound logistics expertise
• Housekeeping skills
• Pharmaceutical care understanding
• GMP knowledge
• Clinical trials awareness
• Chemistry understanding
• Packaging skills
• Import logistics experience
• Biopharmaceuticals knowledge
• Export & logistics understanding

This role offers a challenging and rewarding environment for individuals looking to develop their skills in the pharmaceutical industry.

Clinical Research Coordinator Role

As a Clinical Research Coordinator, you will play a crucial role in the successful execution of clinical trials. This position requires a high degree of organizational skills and attention to detail.

The primary responsibilities of this role include:

1. Subject Recruitment and follow-up activities are coordinated by Clinical Research Coordinators. They ensure that potential participants are approached and recruited for research studies.
2. Research documentation and administrative duties form a significant part of the job. This includes maintaining accurate records, preparing reports, and managing databases.

Key Responsibilities:

1. Clinical Research Coordinators conduct various research study activities such as patient recruitment, data collection, and data management. This involves interacting with patients, collecting data, and ensuring its accuracy.
2. Coordinators also assist in data collection from electronic health records. This involves retrieving relevant information, verifying its accuracy, and updating records accordingly.
3. Maintaining study investigator files is another critical responsibility. This includes storing consent forms, blood collection records, and other relevant documents.
4. Clinical Research Coordinators maintain study records in databases like Redcap and electronic health record systems. This involves regular updates, ensuring data integrity, and adhering to regulatory requirements.
5. Liaising with investigators, clinicians, and laboratory teams is essential for setting up clinical workflows at multiple departments. This involves coordinating efforts, communicating effectively, and resolving any issues that may arise.
6. Preparing necessary documentation for audit purposes is a critical task. This involves gathering information, organizing it, and presenting it in a clear and concise manner.
7. Finally, Clinical Research Coordinators coordinate the submission of new IRB applications, study amendments, and annual reports. This involves ensuring compliance with regulations, meeting deadlines, and maintaining accurate records.

Requirements:

• A Bachelor's Degree in Science, Public Health, or Social Science is required for this position.
• Candidates must be able to adapt to a fast-paced environment and work efficiently under pressure.
• Familiarity with Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA) is essential.

Project Management Specialist

The Clinical Trial Project Manager role performs a lead position for multiservice global clinical trials. The position collaborates with sponsors and oversees the timeline and project deliverables. This role coordinates all services contracted for the study. Project Managers are also responsible for leading cross-functional teams of clinical monitoring, study start-up, regulatory, contract, safety, medical monitoring etc.

Requirements

• A Bachelor's degree in a health-related field;
• At least two years of clinical trial management experience in the Asia Pacific region, preferably in a CRO environment;
• Experience in Infectious Disease/Ophthalmology/Neurology studies is preferred;
• Excellent communication skills including good written and spoken English;
• Flexible, accountable, and comfortable in working in a global environment.

Press Tab to Move to Skip to Content Link
Select how often (in days) to receive an alert:
National Cancer Centre of Singapore Pte Ltd
Senior / Manager (Clinical Trials Contract)
Job Category: Research
Posting Date: 12 Aug 2025
We are seeking a Senior / Manager with professional experience and skills to contribute to the development of the clinical trial program at the National Cancer Centre Singapore (NCCS). The role primarily involves supporting our Clinical Trials Office in reviewing and finalizing contracts related to clinical trials within the Division of Clinical Trials & Epidemiological Sciences (CTE).
Main Duties:
Review clinical trial contracts and collaborate with the SingHealth Legal Department to negotiate agreement terms with sponsors, CROs, academic institutions, or international trial groups.
Verify hard copy contract documents and coordinate signatures from NCCS signatories.
Monitor agreement timelines and follow up on pending responses.
Supervise and advise the Feasibility Team during NDA negotiations, and serve as backup during manpower shortages.
Approve online payments in APIMS, manage training applications in PeopleConnexion (SuccessFactors), and other assigned online applications.
Oversee financial and insurance reporting to CTCC and annual NMRC reporting.
Assist in the submission and updates on clinicaltrials.gov, and manage archiving costs and payments.
Maintain secure filing of executed contracts to ensure confidentiality and prevent loss or damage.
Perform additional duties as assigned by supervisors or senior management.
Main Requirements:
A recognized degree with 6 to 8 years of relevant experience in negotiating clinical trial or research study contracts, including staff supervision.
Knowledge of clinical trial conduct procedures is preferred.
Familiarity with laws and regulations such as HBRA, Medicines Act, Clinical Trial Regulation, PDPA, and ICH GCP.
Excellent communication and writing skills, with strong team and people skills.
Proven leadership and management abilities.
#J-18808-Ljbffr

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