Job Description
Job Description - Providing operational support for execution of clinical trials including (not limited to): - Liaising with doctors/consultants or investigators conducting the trial - Assisting with protocol development - Assisting with CRF development - Planning and participating in investigator meeting - Overseeing the setup of the trial site - Keeping supplies stocked - Patient enrollment tracking - Evaluating and monitoring the site performance - Preparing study documents: Monitoring Manual, Laboratory Manual, Pharmacovigilance plan, informed consents - Periodically reviewing data to identifying potential issues that could signal problems with data - Ensuring adherence to GCP, SOPs, and study protocols - Coordinating data management activities - Generating informed consent forms and site-related materials as needed - Recording results - Assisting with analyzing results - Assisting with study report completion
Requirements
Requirements - Fluency in English - A Bachelor’s degree (minimum) in life science or health care related sciences - Outstanding communication skills and the ability to function within a team environment - Effective negotiation and interpersonal skills - Problem Solving - Quick change of job knowledge - Excellent command of MS Office (PowerPoint, Excel, word) - At least 2 years’ experience of relevant experience - Ready to travel on a regular basis
Employment Type
- Full Time
Job Category
Seniority
Details
Employment type
- Full Time
Job Category
Educations
Seniority
