At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an workplace 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.”
YOUR TASKS AND RESPONSIBILITIES:
- Medical monitoring activity which includes eligibility assessment based on inclusion, exclusion criteria and detailed medical history, review of study endpoint data review and safety investigations.
- Preparation of synopsis, protocol, Clinical Study Report (CSR) and present the proposals in subject’s expert committee (SEC) regulatory meeting.
- Collaborate with clinicians,
KOL to get the feedback and inputs on clinical trial design, comparator and endpoints of the study to finalize synopsis.
- Review of patient eligibility and approval of patients through Interactive Response Technology (IRT) system
- Work with data management team to review timely data extract and participate in data cleaning activities to ensure timely database lock and release of tables, figures, and listings (TLFs).
- Training the study team on protocol and applied aspect of the protocol to clarify the relevance and criticality of each activity considering the study endpoints.
- Interact with investigator to resolve the queries related with protocol from the sites and Ethics Committee.
- Review of AE and SAEs forms and provide review comments in timely manner
- Medical writing of scientific documents
- Planning publications activities for clinical journal manuscripts, clinical journal abstracts, and study article. Identify additional clinical data analysi
📌 Manager - Medical Science (India)
🏢 Sun Pharmaceutical
📍 India
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