168 Clinical Trials jobs in Singapore

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.

We are seeking a Senior Project Management Specialist to oversee multi-site clinical trials from initiation to closure. The ideal candidate will collaborate with various stakeholders, ensuring seamless operations and compliance with regulatory requirements.

This role encompasses:

• Managing multi-site clinical trials
• Monitoring trial progress and guaranteeing timely funding and payment throughout the trial duration
• Liaising with vendors and drug companies for outsourced activities, clinical supplies, and issue resolution
• Reviewing and maintaining the trial master file
• Working closely with sites as the primary point of contact for operational activities

• Bachelor's degree in life sciences or a related field
• At least 4 years of clinical trial experience, including a minimum of 1 year of clinical trial management experience
• Required CRA experience
• Excellent time management skills and ability to handle multiple priorities independently

A highly motivated and detail-oriented Research Nurse is required to assist our team in various aspects of research projects. This role involves providing support to the research team, screening and recruiting suitable patients, briefing patients on research background, collecting data from medical records and research statistics, documenting adverse events, and performing phlebotomy when required.

• Assist in the conduct of clinical trials
• Screen and recruit suitable patients for research projects
• Brief patients on research background and obtain their consent
• Collect and document data from medical records and research statistics
• Perform phlebotomy and venepuncture when required

• Degree in Nursing, Life Sciences, Biomedical Sciences, or related field
• Valid SNB and BCLS certification
• Strong understanding of clinical research ethics and patient confidentiality
• Detail-oriented with good documentation and data entry skills

This is an excellent opportunity for a skilled Research Nurse to join our team and contribute to the success of our research projects.

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

We 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 research

The 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.

The successful candidate will provide and coordinate nursing care to patients who participate in research studies, enforcing standards of care and professional codes of conduct.

This role requires a high level of expertise in clinical trials and the ability to ensure the safety and well-being of study subjects.

We are seeking an experienced and skilled nurse to join our team as a Senior Clinical Nurse in Research Specialization.

National Cancer Centre of Singapore Pte Ltd

Job Category: Administration

Posting Date: 22 Mar 2025

About Us

The National Cancer Centre Singapore (NCCS) is a leading national and regional tertiary cancer centre, attending to the majority of cancer cases in Singapore’s public healthcare sector. We offer world-class oncology care by having the best talent, doing robust clinical and translational research and leading education efforts to improve cancer outcomes. Join us to build a meaningful career and offer patients hope for a cancer-free tomorrow.

About the Role

As a Senior Associate / Associate Executive, you are responsible for Clinical Trials Management in terms of:

1. Maintaining master records in relevant systems such as SAP, OAS, and APIMS.
2. Extracting information from the relevant information systems to prepare the necessary statements and journal vouchers.
3. Coordinating with coordinators and CTE Finance on information verification such as payment requisitions and patient bills.
4. Performing administrative tasks as assigned by Supervisor.

Job Requirements

1. At least 2 years of experience in accounting.
2. Meticulous and observant with an eye for detail.

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

Clinical Research Coordinator

Description

• Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.
• Responsible for working with the principal investigator to meet or exceed study enrollment.
• Reviews the study design and inclusion/exclusion criteria with physician and patient.
• Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance.
• Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review. Monitors data for missing or implausible data.
• Ensures that adequate and accurate records are maintained for inspecting.
• Creates study specific tools for source documentation when not provided by sponsor.
• Collects, completes, and enters data into study specific case report forms or electronic data capture systems.
• Generates and tracks drug shipments and supplies as needed.
• Reports and follows up on serious adverse events as necessary.
• Implements study-specific communications.
• Ensures timely adherence to protocol requirements.
• Responsible for completion of all required documentation according to site works guidelines.
• Ensures timely and accurate data completion.
• Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, subject logs and study-related communications.
• Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations.
• Communicates all protocol-related issues to appropriate study personnel or manager.
• Attends study specific on site meetings, Investigator meetings, conference calls and monthly CRC meetings as required or asked to do so.
• Apprises principal investigator, Research Operations Director and Regional site manager of all study specific medical issues for guidance.
• Maintains patient confidentiality according to ethical and legal requirements.
• Assists in providing coverage for satellite clinic sites as necessary or asked to do so.
• Practice and adhere to the 'Code of Conduct' philosophy and 'Mission and Value Statement.'

Requirements

• Min Degree, preferably in Science / Life Sciences / Public Health / Health Sciences / Pharmacy / Medicine / Nursing or similar from an accredited university
• No exp needed, full training provided
• At least 1-2 years of working experience within clinical research settings (e.g. clinical research associate, study coordinator, or research administrator) is advantageous but not essential
• Knowledge of GCP guidelines and applicable regulations and guidelines of clinical research, or ethical principles relating to human biomedical research
• Able to work independently, as well as part of a team
• Able to work with a high degree of accuracy and attention to detail
• Possess excellent analytical, organisation, communication, and interpersonal skills

If you are interested in the position, do kindly drop your most updated resume to (Attn: Clinical Research Coordinator)

Thank You.

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