
Clinical Research Coordinator
5 days ago
The Medical City Ortigas is searching for an experienced Clinical Research Coordinator to join the team and help lead the organization to the next level. This role is directly responsible in assisting in the functioning of the Institutional Review Board office by processing research protocols submitted by pharmaceutical companies and TMC staff, maintaining files, coordinating meetings, preparing correspondence, facilitating the settlement of IRB fees, acting as liaison to project proponent, distributing protocols, ensuring that reports are submitted by the project proponents in timely manner, and monitoring the conduct of clinical trials.
What's The Role All About?
Job responsibilities include, but not limited to:
Providing administrative support to the IRB Chairman and Medical Services Group Administrative Manager in daily operations
Ensuring confidentiality of all study materials is strictly observed.
Managing and coordinating clinical trial-related activities in the hospital
Benchmarking and researching promptly on latest clinical trial industry standards
Implementing clinical trial trainings, workshops, and activities to clinical trial teams
Conducting quality and completion checks of clinical trial files and legal documents prior to review endorsement
Ensures that sufficient information for patients regarding clinical trials are addressed and followed by the project proponents
Ideally, a candidate must have a
Bachelor's Degree or Equivalent Level of any science related course with some research units
, preferably with at least 1 year experience in office work and exposure to clinical trials and basic training in Research
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