Sr. CRA at Global Pharma
Major Global Pharma
About Our Client
Well established International Pharma company. Products available in more than 150 countries.
Find out ideal investigators for the trial and obtain the agreement on the study plan by fully deliberating at the stage of research.
Perform all necessary procedures required by GCP, such as the required for participation in a clinical trial, contract, supply of trial products, provision of safety information related to SAEs, CRF collection, close of a clinical trial, etc in a timely and prompt manner.
Keep track of registered subjects who are participating in the trial (on trial products) and investigators. Also, record the CRF's agreed timeline and take prompt action to discrepancy.
The Successful Applicant
Experience as a CRA minimum 3 years
Team Player, Logical Thinker, Proactive
What's on Offer
Opportunity in Pharma
Innovative drug development