Clinical Research Coordinator / Clinical Research Associate / Clinical Trial Assistant
Company: D365 Champs - A Dynamics 365 & Power Platform Community
- Location: Singapore
- Seniority: Entry level
- Employment type: Part-time
- Posted: 11 days ago
- Offer language: English
Job description
Role Description
The Clinical Research Coordinator / Clinical Research Associate / Clinical Trial Assistant supports the planning, conduct, and documentation of clinical studies in accordance with approved protocols and study procedures. Responsibilities include coordinating study activities, maintaining essential records, tracking progress, and communicating with investigators, study sites, and sponsors.
Clinical Research Coordinator positions support site-level activities, including participant scheduling, visit coordination, and accurate study data collection. Clinical Research Associate positions monitor study sites, review protocol adherence and data quality, and follow up on findings. Clinical Trial Assistant positions provide administrative support, maintain trial documentation, and coordinate meetings and submissions. All positions help protect participant confidentiality, escalate study concerns, and support timely completion of assigned activities.
Qualifications
- Diploma or bachelor’s degree in Life Sciences, Nursing, Pharmacy, Biomedical Science, or a related field.
- Relevant experience in clinical research, healthcare, study coordination, or clinical trial administration.
- Understanding of clinical trial processes, Good Clinical Practice principles, and research ethics.
- Strong attention to detail when maintaining study records and reviewing documentation.
- Ability to coordinate schedules, track study activities, and manage competing deadlines.
- Familiarity with electronic data capture systems, clinical trial management systems, or document management platforms.
- Clear communication skills when working with investigators, site teams, sponsors, and participants within the role’s responsibilities.
- Ability to handle confidential information appropriately and follow established study procedures.
- For coordinator positions, experience supporting participant visits and site activities; for associate positions, relevant monitoring experience and willingness to travel where required.
- For assistant positions, strong administrative and document coordination skills; relevant clinical research training is an advantage.
