169 Medical Writer jobs in Singapore

• Job Code: FLS-PEP 050

Pepgra is seeking freelance specialist medical and clinical writers in Public Health, capable of handling a wide range of disorders including healthcare-associated infections, cardiovascular disease and stroke, HIV/AIDS, nutrition, physical activity, and obesity. Candidates should be highly proficient in English (preferably native speakers from the USA, Europe, or UK) and able to contribute to our clinical research, writing, and editing services.

1. Scientific research and writing in Public Health, including manuscripts (original, experimental studies, case reports, literature reviews, meta-analyses, systematic reviews), clinical documents, regulatory submission documents, evidence-based policy documents, theses, and dissertations.
2. Adherence to specific job instructions.
3. Timely delivery of research and writing tasks.
4. Research industry-related topics and produce plagiarism-free content.
5. Ensure accuracy, proper terminology, flow, transition, and coherence in content.

• Postdoctoral, PhD, or Master's degree, or expertise in Public Health research/writing.
• Experience and preferred certifications in academic writing, editing, publishing, dossier report writing, policy development reports, scientific communication, or journal article writing.
• Knowledge of academic and scientific writing styles and conventions.
• Excellent writing and editing skills with attention to detail.

• Opportunity to develop research writing and editing skills.
• Access to articles on industry trends, publication tips, and a learning platform.
• Insight into worldwide research activities.

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Job Code: FLS-PEP 055

Freelance Specialist Medical Writers and Editors play a vital role in Pepgra's business model by assisting us in ensuring client satisfaction through writing high-quality research and evidence-based policy documents intended for publication in high-impact journals, regulatory submissions, and policy documents across various subject areas.

1. Adhere to job-specific instructions
2. Work within set deadlines
3. Research industry-related topics
4. Deliver plagiarism-free content
5. Ensure correctness of content, terminology, flow, transition, and coherence

1. Research/writing experience with preferred certification in academic writing, editing, publishing, dossier report writing, evidence-based reports for policy development, scientific communication, journal article writing, etc.
2. Knowledge of different styles and conventions in academic and scientific writing
3. Excellent writing and editing skills with attention to detail (prior writing experience is advantageous)

You will develop skills in research writing and gain an understanding of the nuances of editing. You will have access to articles on the latest industry trends and publication tips through our learning and discussion platform. This role provides an inside view into worldwide research activities and evidence-based reports for policy development.

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• Freelance Specialist Medical and Clinical Writer in Sexual Health

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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

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

National Neuroscience Institute of Singapore

Job Category: Research

Posting Date: 11 Jan 2025

We are looking for a candidate who will be providing research support service to the investigators in the conducting and implementation of clinical trial and/or clinical research studies at the National Neuroscience Institute (TTSH campus), in adherence to Singapore Guideline for Good Clinical Practice (SGGCP) and protocol requirements.

There will be opportunities to:

1. Contribute to clinical trials set-up, feasibility and coordination
2. Contribute to data processing and analysis of results for multiple studies conducted within the department
3. Acquire new skillsets, such as imaging handling, processing and analysis
4. Gain experience in scientific writing for presentations and publications

Requirements:

1. Bachelor’s degree in Life Sciences, Psychology or related fields
2. Good communications and interpersonal skills
3. Good IT literacy and statistics skills are also desirable
4. Prior experience in a clinical environment and/or with clinical trials/studies would be most advantageous

Job Responsibilities:

• Manage and execute clinical projects and related administrative tasks in a fast-paced environment.
• Ensure proper documentation and maintain an up-to-date database.
• Perform regular maintenance and calibration of clinical equipment.
• Handle data entry and collect accurate clinical data.
• Plan and schedule subject visits, including coordinating recruitment activities.

Job Requirements:

• Possess at least a Diploma or Degree in a relevant field.
• Able to work independently and meet tight project deadlines.
• Strong team player who can also work with minimal supervision.
• Capable of prioritizing tasks and managing multiple responsibilities efficiently.
• Excellent coordination, communication, and interpersonal skills.
• Able to thrive in a fast-paced environment and handle work-related stress effectively.

To apply for this position, please email your detailed resume, including your current and expected salary, to .

We regret to inform that only shortlisted candidates will be notified.

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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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• 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.

• Manage and execute clinical projects and related administrative tasks in a fast-paced environment.
• Ensure proper documentation and maintain an up-to-date database.
• Perform regular maintenance and calibration of clinical equipment.
• Handle data entry and collect accurate clinical data.
• Plan and schedule subject visits, including coordinating recruitment activities.

• Possess at least a Diploma or Degree in a relevant field.
• Able to work independently and meet tight project deadlines.
• Strong team player who can also work with minimal supervision.
• Capable of prioritizing tasks and managing multiple responsibilities efficiently.
• Excellent coordination, communication, and interpersonal skills.
• Able to thrive in a fast-paced environment and handle work-related stress effectively.