1. Identify and qualify potential investigators to ensure that the sites have adequate time and can fulfill their obligation to the study.
2. Responsible for identification & collection of necessary documents to be forwarded to Project Manager/ designee, in order to check the feasibility of site/ investigator and approval from authorities.
3. Prepare or submit or support other colleagues for Regulatory and EC submissions and in the generation of Financial Agreements according to standard and local country practices.
4. Negotiate study budgets with investigators and ensure that timely payments are made to the site as per guidance from Project Manager.
5. Responsible for training of site study team regarding the monitoring plan, recording & maintenance of essential documents and for start up activities & site initiation as per the guidance of Project Manager.
6. Assist for the preparation and presentation at investigator meetings, as required to ensure that the clinical and investigational site staff team are well informed about the study and related procedures.
7. Conduct of monitoring visits as per monitoring plan in order to check compliance with study management, protocol & other requirements at all assigned sites.
Job Type: Full-time
Salary: ₹500,000.00 – ₹700,000.00 per year
Benefits:
Schedule:
Supplemental pay types:
Ability to commute/relocate:
Education:
Experience:
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