The posting
Key Responsibilities
- Support investigators in the administration and coordination of clinical research activities throughout the study lifecycle, from initiation to completion.
- Recruit and enroll suitable study subjects and monitor their condition throughout the study.
- Perform clinical procedures including vital signs monitoring, biological sample collection and processing, where required.
- Collect, manage and accurately enter research data.
- Work closely with the study team to ensure subject safety and compliance with study requirements.
- Conduct study procedures in accordance with SOPs, study protocols, instruction manuals, applicable regulations and ICH-GCP guidelines.
- Attend investigator meetings, including local and overseas meetings, as assigned.
- Participate in site initiation meetings and liaise with relevant internal and external stakeholders throughout the study.
Requirements
- Degree in Science or Nursing. Candidates with a Diploma may be considered for an Associate-level position.
- Registration with the Singapore Nursing Board (SNB) is required for State Registered Nurses.
- Minimum 2 years of experience in coordinating clinical research activities.
- Strong interest in clinical research and healthcare innovation.
- Good team player with strong interpersonal and communication skills.
- Strong problem-solving and organisational abilities.
- Able to work independently while collaborating effectively with multidisciplinary teams.
Interested candidates please send a copy of your resume in MS Word to [email protected]
Cheryl Lee
Outsourcing Team
Company Reg. No. 199601303W
EA Licence No. 99C4599



