228 Vaccine Development jobs in Singapore

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

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.

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 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 Trials Monitoring Manager (US Pharma MNC, Regional, Global Study Mgmt)
Design, plan and conduct clinical research trials by effectively coordinating the activities of study coordinators and investigators and by ensuring compliance with study protocols, FDA and International regulations, IRB and/or Ethics committees requirements and overall clinical objectives.
Responsibilities
• Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements.

• Develop and deliver technical training on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements as well as training and proctoring new employees on trial and study related activities.
• Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Boards, Contract, and Training, developing process improvements.
• Contribute to the development of clinical protocols, informed consent forms, and case report forms. Also contribute to team projects.
• Validate investigational device accountability by tracking the history of investigational devices to the field sites and through final disposition.
  Qualifications
  • Bachelor’s degree in Life Sciences or related field is highly preferred. Associates or equivalent 5-10 year clinical degree in Life Sciences or related field or equivalent in work experience is required. GCP/ Clinical research certification is strongly preferred (ACRP or SoCRA, Clinical Coordinator/CRA certification).
• Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are a must.
• Knowledge of FDA regulatory requirements related to the conduct of clinical studies.
• Work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors
• Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

If you are interested in the position, do kindly drop your most updated resume to
(Attn: Clinical Trials Monitoring)
Thank You.
Leon Leong De Cong
R
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599
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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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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.
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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