169 Medical Writers jobs in Singapore

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.

Job Summary:

This role involves coordination and administration of research studies, focusing on recruitment, data collection, and management.

Key Responsibilities:

• Participate in subject recruitment, scheduling, and data entry processes, adhering to study protocols.
• Screen patients based on eligibility criteria and communicate the study's objectives in a clear and concise manner.
• Obtain informed consent, administer study questionnaires, and ensure timely follow-up with study participants.
• Collaborate closely with the research team, clinicians, clinic staff, and relevant departments to guarantee research study needs are met.
• Manage multiple tasks simultaneously, set realistic targets, and achieve research deliverables within tight timelines.
• Conduct research activities including patient recruitment, data collection, and data management.
• Assist in extracting data from electronic health records and maintain accurate records in databases such as Redcap and electronic health record systems.
• Maintain adherence to strict research protocols, including those related to patient confidentiality and data security.
• Liaise with investigators, clinicians, and laboratory teams to establish efficient clinical workflows at various departments for research recruitment purposes.
• Prepare necessary documentation for audit purposes and coordinate submissions of new IRB applications, study amendments, and annual reports.
• Ensure highest standards of professional conduct, record-keeping, and adherence to hospital policies, ethics requirements, and local regulations.

Job Scope

•    To ensures proper management of Investigational Product Controlled Drug Therapeutic Product , which includes sourcing, receipt, storage, preparation, dispensing, labelling, inventory accountability, reconciliation, retention, destruction and documentation, etc.

•    To Perform extemporaneous preparation, aseptic compounding and other dispensing activities.

•    To Perform pharmacy operational activities such as inventory management, ensuring cleanliness of pharmacy areas, and environmental monitoring.

•    To ensure proper management of randomization and unblinding procedures for blinded clinical trials.

•    To ensures proper handling and facilitates maintenance of equipment in the pharmacy.

•    To Perform cross-functional and other duties as required.

Qualification

•    Singapore Registered Pharmacist.

•    Experience in compounding, or working in cleanroom or manufacturing setting (preferred).

Interested candidates please send in your resume to:

 
EA Personnel: Valerie Yong Kian Fung
CEI No.: R1103704
Recruit Express Pte Ltd, EA License No.: 99C4599

We are seeking a skilled and detail-oriented research coordinator to join our team. In this role, you will be responsible for coordinating clinical trial activities in accordance with the study protocol and ICH Good Clinical Practice guidelines.

• Patient recruitment and screening,
    • Monitoring subject compliance to treatment and follow-up,
    • Data collection and management including resolving data discrepancies,
    • Coordinating biological specimen collection,
    • Adverse event monitoring and safety reporting,
    • Maintaining investigator site files and submitting to relevant authorities,
    • Tracking trial expenditures and invoicing.

• Degree in Life Sciences or Nursing
• OR Diploma in Nursing with minimum 6 years working experience as CRC
• 2 years of related working experience 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

The ideal candidate will possess excellent organizational and communication skills, with the ability to work effectively in a team environment. A strong attention to detail and the ability to maintain confidentiality are essential for this role.

• Ongoing training and development opportunities
• Opportunity to work on challenging projects
• Collaborative and dynamic work environment