Hyderabad

Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts, Clinical Research Associate at Sun Pharma

The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. The position requires working cross-functionally within the site and other functions to deliver on technical objectives.

Proven track record of leading a large, geographically diverse sales team, including at least 2 years of experience overseeing half of India with consistent performance, growth and positive P&L outcome.

Proven track record of leading a large, geographically diverse sales team including experience overseeing half of India - South & West with consistent performance, growth and positive P&L outcome.

GCP Subject Matter Expert, Provide independent and objective quality advice in support of clinical trial activities and in line with current standard methodology. Experience in Quality Management, Quality Assurance. pharmaceuticals

Deliver non-interventional studies, research collaborations, and investigator-initiated trials, managing spend and forecasts. Represent Study Management operations at Therapy Area Medical Affairs Team meetings.

Manage core HEVA communication processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with Core Value Dossier, the US AMCP dossier, and HEVA contributions as appropriate to other submissions

Review and approve development protocols, reports, and technical documents for formulation, analytical, and process development.

Preferably Pharm.D with Experience in Coordinating and conducting clinical trials. Conducting and coordinating clinical trials in the department of Medical Oncology.