Recruit and Develop CRAs and implement necessary actions to improve their performance.
Lead quality clinical trial projects (CDP and/or local) in the country.
Provide trial related communication and insight to key internal and external stakeholders.
Coordinate the clinical trial set-up in partnership with the COM.
Maintain ongoing communication with Ethics Committees and the Health Authority, ensuring the Central and local (as applicable) Ethic Committee is provided with the documents requested.
Qualification & Experience
8 to 10 years of experience in managing global clinical trials as CRA/Sr. CRA (approx. 6 yrs) and Team lead/Trial Manager (aprox. 2 yrs)
Currently leading/managing project team of CRAs and or CTAs
Candidates with prior experience in handling Diabetes/Obesity/OSCD (Other Serious Chronic Diseases)/Hemophilia/Growth Hormone disorders trials will be preferred