At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key responsibilities:
- Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts
- Preparation and submission of study documents for EC permission for respective study across centers
- Oversee & document IP dispensing, inventory management & reconciliation
- Ensure timely site initiation, site monitoring, and site close-out activities are performed and respective reports are generated
- Investigator and site personnel training on the Study protocol, procedures, and GCP principles
- Ensure timely recruitment of trial participants and subsequent efficient and effective data entry, source data verification and query resolution
- Ensure timely reporting of SAEs, SUSARs, and reporting of SAEs to all sites and investigators in alignment with regulations and Suns PV policies
- Risk identification, analysis, and CAPA for sites not meeting expectations as per the plan
- Co-ordinate with in-house or CRO partners for data management, statistical analysis, statistical analysis report & DBL
