146 Clinical Research jobs in Singapore

Precision for Medicine is not your typical CRO. At Precision for Medicine, we combine new technologies, expertise, and operational scale to improve the speed, cost, and success rate of bringing life-changing therapies to patients. We focus on Oncology and Rare Diseases, integrating clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences.

We pride ourselves on high CRA retention rates, a supportive culture, and a work environment where your voice is heard. Our smaller size allows for greater influence, manageable protocols, and a better work/life balance with reasonable travel requirements.

We are seeking an experienced CRA or Senior CRA for our team in Singapore. The ideal candidate will have prior monitoring experience in Oncology clinical studies conducted in Singapore.

This position is remote (homebased anywhere in Singapore) with travel to sites for monitoring visits.

About you:

• You are calm, thoughtful, and responsive when challenges arise.
• You are well-prepared and proactive in meetings, site visits, and updates.
• You find creative solutions to overcome difficulties.
• You have a keen eye for detail.
• You can identify risks and propose mitigation strategies.
• You take responsibility for the quality and outcomes of your work.
• You handle conflicts effectively using proven resolution strategies.

Responsibilities include:

Monitoring and managing clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations. Coordinating activities such as site identification, regulatory submissions, pre-study and initiation visits. Supporting larger trials and mentoring junior staff. Interacting directly with clients, managing payments, and contributing to proposals and presentations.

Requirements:

• Life science degree or equivalent experience.
• CRA experience in Oncology within CRO or pharmaceutical industry, with at least 1 year in Oncology monitoring.
• Availability for domestic travel, including overnight stays; international travel may be required for senior roles.

Preferred:

• Graduate or postgraduate degree in a scientific or healthcare field.
• Over 2 years of oncology experience.
• Experience with study startup activities.
• For Senior CRAs, financial management and mentoring experience are desirable.

Join us to contribute to groundbreaking cancer therapies, with a culture that values your contributions, ideas, and growth. We are committed to diversity and equal opportunity employment, with accommodations available for applicants with disabilities.

Precision for Medicine is not your typical CRO. We combine new technologies, expertise, and operational scale to enhance the speed, cost, and success rate of bringing life-changing therapies to patients. Our approach uniquely integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences, with a strong focus on Oncology and Rare Diseases.

We pride ourselves on high CRA retention rates, a supportive culture, and a work environment where your voice is valued. Our smaller size allows for greater influence, manageable protocol loads, and a better work/life balance, with reasonable travel requirements.

We are seeking an experienced CRA or Senior CRA for our team in Singapore. Previous monitoring experience in Oncology clinical studies within Singapore is required.

This is a remote, home-based position in Singapore, with travel to sites for monitoring visits.

About you:

• You are calm, thoughtful, and responsive, especially when facing challenges.
• You are well-prepared and proactive for investigator meetings, site visits, or team updates.
• You excel at overcoming difficulties creatively and efficiently.
• You have a keen eye for detail and can identify study risks, proposing mitigation strategies.
• You take responsibility for the quality and outcomes of your work.
• You handle conflicts effectively using proven resolution strategies.

Role responsibilities include:

Monitoring clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations. Coordinating study setup activities, supporting larger trials, mentoring junior staff, and interacting directly with clients, including payments and proposals.

Requirements:

• Life science degree or equivalent experience
• At least 1 year of CRA experience in Oncology within Singapore
• Availability for domestic travel, including overnight stays; international travel may be required for senior roles

Preferred qualifications include a postgraduate degree, over two years of oncology experience, study start-up experience, and financial management or mentoring experience for senior roles.

Join us to contribute to groundbreaking cancer therapies, be valued for your contributions, and grow within our organization.

About Precision for Medicine:

We are a precision medicine CRO, integrating novel clinical trial designs, operational and medical expertise, biomarker and data analytics, and a passion for rare diseases and oncology. Our work leverages molecular insights and advanced technology to optimize oncology development pathways.

We adhere to all applicable privacy laws and are committed to equal opportunity employment. For accommodations or concerns about fraudulent job offers, contact us directly.

3 months ago Be among the first 25 applicants

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 Senior Clinical Research Associate (SCRA) 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 the implementation of 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 with 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.
• Manage trial sites utilizing both on-site and off-site activities including: o Verification of quality, accuracy, completion, and timeliness of data.
• 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.
• Coordinate and perform translation verification of regional language, as required or as applicable per region.
• Perform site close-out visits and other site activities including archiving, as applicable.
• Mentor, coach, and train junior staff members as directed by line management.
• Perform any additional responsibilities assigned by the Line Manager and/or Project Lead.

About You

• Educated to degree level in pharmacy, medical, nursing, biological science, or other health-related disciplines preferred or equivalent relevant experience.
• ≥5 years’ experience preferred, but ≥4 years may be considered based on relevant experience in clinical trial monitoring and/or site management within an academic, contract research organization, or pharmaceutical environment.
• Displays high 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 high competence in the following skill areas: negotiation and conflict resolution, critical thinking, problem-solving, decision making, and strategic thinking. Ability and willingness to travel.
• Ability to be flexible and adaptable in the face of changing organizational priorities and ambiguous environments.

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
• Industries Pharmaceutical Manufacturing

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(Senior) Clinical Research Associate page is loaded(Senior) Clinical Research Associate Apply locations Singapore time type Full time posted on Posted Yesterday job requisition id R1458967

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.

#LI-Hybrid

#CRAFSAJD

#CRASDAJD

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

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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Job Category: Research

Posting Date: 27 Mar 2025

Job Description:

You will provide research support service for clinical research, in accordance to the applicable regulatory, Good Clinical Practice and protocol requirements. You will work closely with the Principal Investigators (PIs), to assist them with organisation of study initiation meetings, IRB submission, protocol development, preparation of study logistics, recruitment, data collection and management, study documentation, study monitoring and other duties as assigned.

You will support and participate in the SGH mission of providing quality patient care, education, and research.

Job Requirements:

1. Bachelor Degree in Nursing/Science or Diploma in Clinical Trials Management
2. Fresh graduate or with at least one year of relevant experience
3. Proficient in using MS Office software
4. Effectively bilingual
5. Excellent oral and written communication skills

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• Assist the investigators in overall administration of clinical research activities prior to, during, and post-study, such as enrolling suitable subjects, taking vital signs, collecting and processing biological samples, collecting and entering data, and monitoring subjects’ condition.
• Work with the study team to ensure subjects’ safety.
• Carry out the required procedures according to the SOP, study protocol, and Instruction manual(s) in compliance with the Regulations and ICH Good Clinical Practice Guideline.
• Attend investigator’s meetings (local/overseas) and site initiation meetings as assigned, and liaise with relevant internal and external agencies during the course of work.

• Degree in Sciences/Nursing. Those with a Diploma will be considered as Associate.
• Registration with the Nursing Board, Singapore (applicable to State Registered Nurse only).
• At least 2 years’ experience in the coordination of clinical research activities.
• Good team player.
• Problem-solving skills.

Only shortlisted candidates will be notified.

As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.

You will support and assist the Principal Investigator in the following trial related activities:

• Patient screening and recruitment,
• Monitoring subject’s compliance to their treatment and follow-up,
• Data collection and management including resolving data discrepancies,
• Coordinating the collection of biological specimens,
• Monitoring of adverse events and safety reporting,
• Maintaining and organising of investigator site files, preparation and submissions to the ethics committee and relevant local health authorities,
• Tracking of trial expenditures and timely invoicing.

Requirements:

• Degree in Life Sciences/Nursing
• OR Diploma in Nursing with minimum 6 years working experience as CRC
• 2 years of related working experience will be advantageous
• Excellent time-management and communication skills
• Able to work independently and as a team
• Detail-oriented and self-motivated
• Good grasp of MS Office applications

National Cancer Centre of Singapore Pte Ltd

Job Category: Research

Posting Date: 15 Jan 2025

As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance with the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.

You will support and assist the Principal Investigator in the following trial-related activities:

• Patient screening and recruitment
• Monitoring subject’s compliance to their treatment and follow-up
• Data collection and management including resolving data discrepancies
• Coordinating the collection of biological specimens
• Monitoring of adverse events and safety reporting
• Maintaining and organizing investigator site files, preparation and submissions to the ethics committee and relevant local health authorities
• Tracking trial expenditures and timely invoicing

Requirements:

• Degree in Life Sciences/ Nursing/ Biomedical Science/ Biological Sciences
• 1-2 years of related working experience will be advantageous
• Good time-management and strong ability to multi-task
• Able to work independently and as a team
• Conscientious, meticulous, and self-motivated