Clinical Project Manager
發佈於： 2024/10/27
Taipei
Permanent
生命科學、醫療保健、製藥
Responsibilities:
- Coordinate and support multiple teams to ensure clinical trial operations run smoothly.
- Facilitate effective communication across teams, including clinical sites, CROs, and company management.
- Engage with CRA/CPM from contracted CROs and Principal Investigators/Site Coordinators at clinical sites to optimize patient recruitment strategies.
- Conduct routine monitoring of clinical sites and contracted CROs to oversee proper PK/PD sample collection and analysis processes.
- Compile, analyze, and summarize clinical data to create comprehensive reports.
- Handle additional tasks as assigned by the supervisor.
- Academic background in biomedical sciences or related fields. Proven experience (3-4 years) in clinical operations or research, particularly within new drug development studies.
- Strong organizational skills to manage study data, reports, documentation, and records.
- Demonstrated adaptability and eagerness to acquire new skills and knowledge relevant to project needs.
- Proficiency in communication and interpersonal skills.
- Foundational skills in report writing and presentations.