384 Clinical Research Associate jobs in Singapore

Direct message the job poster from HiRO - Harvest Integrated Research Organization

• At least 3 years of experience as a Clinical Research Associate (CRA)
• Availability for 12-16 hours per week (0.3-0.4 FTE)
• Strong English communication skills (Chinese proficiency preferred but not mandatory)

Responsibilities:

• Conduct monitoring visits (remote/on-site as needed)
• Ensure compliance with study protocols and regulatory requirements
• Collaborate with investigators and study teams

Interested candidates, please submit your CV to

• Seniority level Associate

• Employment type Part-time

• Job function Research

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Job Title: Clinical Research Associate

We are seeking a highly motivated and detail-oriented individual to join our team as a Clinical Research Associate.

Responsibilities:

• To assist the principal investigator in developing and implementing clinical research protocols
• To prepare and submit regulatory documents for approval
• To facilitate the signing of project agreements with external collaborators
• To implement and monitor programme activities and workflow
• To conduct surveys or questionnaires
• To manage study-related equipment and handle queries from research subjects

Requirements:

• Degree in Nursing, Biological Science, Pharmacy or other healthcare related discipline
• Able to work independently and adapt in a fast-paced environment

Benefits:

This role offers the opportunity to work on exciting clinical research projects and develop valuable skills in clinical trials management. If you have a passion for research and are looking for a challenging role, we encourage you to apply.

Contact Information:

Please send your resume to for consideration.

This role is ideal for individuals who enjoy working in a fast-paced environment and are passionate about advancing medical research.

1. Key Responsibilities:

• We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team. The successful candidate will be responsible for coordinating clinical trials, managing databases, and ensuring compliance with regulatory requirements.

About the Job:

Job Title: Clinical Research Coordinator

Key Responsibilities:

• Coordinate clinical trials from start to finish, including site selection, patient recruitment, and data management;
• Develop and maintain accurate and detailed databases, spreadsheets, and other tools to track trial progress and participant information;
• Maintain strong relationships with sites, investigators, and other stakeholders to ensure timely and efficient trial conduct;
• Ensure adherence to Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and other regulatory guidelines;
• Collaborate with cross-functional teams to identify and implement process improvements;
• Provide education and support to sites and participants on trial procedures and protocols;
• Assist in the development of study-related documents, such as informed consent forms and case report forms;
• Perform other duties as assigned by management.

Requirements:

To be successful in this role, you will need:

• A bachelor's degree in a life science or related field;
• At least 1 year of experience in clinical research coordination or a related field;
• Excellent communication, organizational, and interpersonal skills;
• Able to work independently and as part of a team;
• Strong attention to detail and ability to manage multiple priorities;
• Familiarity with electronic data capture (EDC) systems and clinical trial management software (CTMS);
• A valid driver's license and reliable transportation.

What We Offer:

We offer a competitive salary, comprehensive benefits package, and opportunities for career growth and professional development. If you are a motivated and detail-oriented individual who is passionate about advancing medical research, we encourage you to apply for this exciting opportunity.

About Us:

We are a leading organization dedicated to improving human health through innovative research and development. Our team is comprised of talented professionals who share a common goal of making a positive impact on people's lives.

Job Title: Clinical Research Studies Assistant

• Conduct comprehensive literature reviews and assist in compiling research findings
• Support data collection, data entry, and basic statistical analysis
• Coordinate meetings, documentation, and ethics submissions related to research projects
• Assist in preparing reports, presentations, and manuscripts for research publications
• Perform general administrative duties to support the research team

• Bachelor's degree in Social Science, Public Health, Psychology, or Nursing
• Prior experience in research or healthcare projects is an advantage
• Familiarity with research methodologies and ethical guidelines
• Proficient in Microsoft Office and data analysis tools (e.g. STATA, SPSS, Python, R, Excel)
• Strong organisational skills with attention to detail
• Good communication and interpersonal skills to work with diverse stakeholders
• Self-motivated, able to work independently and in a team
• Able to manage multiple tasks and meet tight deadlines

This is an exciting opportunity to support research teams in conducting clinical studies. As a Clinical Research Studies Assistant, you will play a key role in assisting with research-related activities.

As a valued member of our team, you will have the opportunity to contribute to the success of our research projects and make a meaningful impact in the field of clinical research.

As a Research Coordinator, you play a vital role in the success of clinical trials.

Clinical Research Coordinators are essential to the execution of clinical trials. In this part-time position, you will support investigators by recruiting and managing study participants effectively.

• Recruit and screen participants, ensuring strict adherence to study protocols and regulatory requirements.
• Coordinate specimen collection and dispatch, monitor adverse events, and report safety concerns.
• Manage study data entry and validation, extracting relevant information from medical records and reporting adverse events.
• Prepare and sort data for entry and maintain high-quality data levels to optimize team efficiency.
• Resolve incomplete or discrepant data.
• Coordinate scheduling and visits for stakeholders and participants, including logistics and finances.
• Provide administrative support as required.

Seeking a highly skilled and dedicated Research Fellow to join our team.

As a Research Fellow, you will play a key role in supporting the design, execution, and analysis of clinical and translational research projects.

Main Responsibilities

• Design and refine clinical or population-based research protocols to ensure high-quality results.
• Collaborate with clinicians, data analysts, lab personnel, and institutional research offices to implement efficient study protocols.
• Develop study objectives, inclusion criteria, methodology, and outcome measures through collaborative efforts.
• Propose new studies by planning, preparing study protocols, and implementing these studies efficiently.
• Conduct statistical analyses, clean, and interpret datasets using advanced statistical tools.
• Prepare and present data and insights at various relevant forums to drive decision-making.
• Collaborate on manuscript preparation for submission to peer-reviewed journals through literature review, data analysis, and drafting.
• Provide guidance to junior research staff, interns, or medical students supporting the project.

Additional Responsibilities

• Work closely with cross-functional teams to bridge clinical and scientific information into actionable insights.
• Attend regular team meetings, journal clubs, and collaborative planning sessions to drive project success.
• Stay up-to-date with industry trends and best practices to continuously improve research methods and outcomes.

As a skilled Clinical Research Coordinator, you will be responsible for assisting investigators in clinical research projects. The ideal candidate will possess strong knowledge of clinical research principles and excellent organizational skills.

• Key Responsibilities:

Join to apply for the Clinical Research Associate II role at Emerald Clinical

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Join to apply for the Clinical Research Associate II role at Emerald Clinical

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At Emerald Clinical, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.

Our therapeutic expertise spans renal, cardiometabolic, and oncology—areas where we make a significant impact on improving global health.

At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.

Why Join Us?

At our core, Emerald Clinical is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

Here’s what makes us stand out:

• Purpose-Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.

• Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.

• Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.

About the Role

The Clinical Research Associate 2 (CRA2) is a member of the Clinical Operations group at Emerald Clinical. The Clinical Operations group is responsible for site management, monitoring tasks, and the operational support of clinical trials. The group allocates resources to projects as appropriate to assist with implementing project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures (SOPs)

Your Responsibilities

Coordinate the identification, feasibility assessment, and selection of investigators and sites to undertake the trial.

Complete all monitoring activities per the Monitoring Plan along with completing monitoring visit reports, accurately and within the predetermined timeframe.

Prepare, plan, organize, and conduct site evaluation visits and report on these visits to assist in site selection.

Prepare, submit, and/or liaise with regulatory specialist colleagues, regarding the preparation of regulatory packages, importation/exportation requirements, and updates of Ethics Committee packages.

Negotiate site budgets, coordinate for site contract execution, track invoicing, and ensure timely site payments.

Prepare, plan, organize, and conduct site initiation visits.

Develop and maintain appropriate monitoring tools and project-specific documents.

Motivate and train investigators to ensure that the trial site personnel have a good understanding of the protocol, investigational product, and requirements of the trial so they can fulfill their obligations to conduct the trial accurately and to deadlines. Collect, review, and approve essential documents from trial sites, to ensure quality and compliance, and code documents for Trial Master File (TMF) filing.

Reconcile contents of in-house TMF and site’s Investigator Site Files.

Coordinate distribution, tracking, handling, and destruction of investigational product and other trial supplies per site/trial requirements.

Maintain trial information using the clinical trial management system and any other tracking and reporting tools for the trial.

Support strategies to boost recruitment efforts.

About You

Tertiary qualifications in a related science or health care discipline.

Previous experience in clinical trials within an academic, CRO, or pharmaceutical environment with 3 – 5 experiences in monitoring and site management experience is mandatory

Demonstrate practical knowledge of ICH-GCP guidelines and global and local ethical and regulatory research requirements.

Display competence in the following technical areas: ethical and participant safety considerations, site start-up management, site conduct management, risk management, quality management, supply management, scientific concepts and clinical research design, and issue escalation management.

Demonstrate competence in the following business skill areas: negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking.

Demonstrate solid interpersonal communication, presentation skills, and flexibility to work well within a multi-disciplinary team both autonomously and with a wide range of varying stakeholders

Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments.

Ability and willingness to travel

What We Offer

We understand that great work happens when people feel valued and supported. That’s why we provide:

• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.

• Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.

• Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.

• Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.

• Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.

Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.

• Seniority level Not Applicable

• Employment type Other

• Job function Research, Analyst, and Information Technology

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As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits.

Your responsibilities will include:

• Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation

• Supporting the development of a subject recruitment plan

• Establishing regular lines of communication plus administering protocol and related study training to assigned sites

• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate

• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

• You will need to be comfortable collaborating and communicating with a variety of colleagues and customers . You will need to have a good knowledge of applicable clinical research regulatory requirements.

Qualifications:

• University degree in scientific discipline or healthcare

• At least 1 year of on-site monitoring experience

• Good knowledge of GCP and clinical research regulatory requirements

• Good computer skills including MS Office

• Excellent command of English language

• Organizational, time management and problem-solving skills

• Ability to establish and maintain effective working relationships with colleagues, managers, and customers.

• Flexibility to travel.

What you can expect:

• Working with different customers on global trials

• Career development opportunities for those who are passionate in wanting to grow as part of the organization.

• Leaders that support flexible work schedules/arrangement

• Excellent working environment in a stable, international, reputable company

• Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape

• Attractive remuneration package.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at