Non-Clinical Job at Sun Pharma

Are you looking for a Manager – Medical Science role in Mumbai? Sun Pharma Laboratories Ltd has an opening for this position at its Mumbai location. The Non-Clinical Job covers medical monitoring, preparation of protocols and Clinical Study Reports, and collaboration with clinicians, data management and statistics teams. Candidates need an MBBS with an MD (Pharmacology) or another relevant medical qualification, along with 1-2 years of prior work experience.

About SUN Pharma:

Sun Pharmaceutical Industries Limited (Sun Pharma) is one of India’s leading pharmaceutical companies and a global provider of medicines. The company develops, manufactures, and markets a wide range of pharmaceutical products, including generic and speciality medicines, as well as active pharmaceutical ingredients (APIs).

Sun Pharma operates across several therapeutic areas, including cardiology, psychiatry, neurology, dermatology, oncology, and diabetology. Through its focus on research, innovation, and global healthcare access, the company aims to make quality medicines available to patients in India and international markets.

Job Details:

  • Job Title: Manager – Medical Science
  • Business Unit: MACR
  • Location: Mumbai (Sun House – Corporate Office)

Key Responsibilities:

  • Medical monitoring activity, which includes eligibility assessment based on inclusion and exclusion criteria and detailed medical history, review of study endpoint data, and safety investigations.
  • Preparation of synopsis, protocol, Clinical Study Report (CSR) and present the proposals in the subject’s expert committee (SEC) regulatory meeting.
  • Collaborate with clinicians and KOLs to get feedback and inputs on clinical trial design, comparator and endpoints of the study to finalise synopsis.
  • Review of patient eligibility and approval of patients through Interactive Response Technology (IRT) system
  • Work with the data management team to review timely data extracts and participate in data-cleaning activities to ensure timely database locking and release of tables, figures, and listings (TLFs).
  • Train the study team on the protocol and its application to clarify the relevance and criticality of each activity, considering the study endpoints.
  • Interact with the investigators to resolve protocol-related queries from the sites and the Ethics Committee.
  • Review of AE and SAEs forms and provide review comments promptly
  • Medical writing of scientific documents
  • Planning publication activities for clinical journal manuscripts, clinical journal abstracts, and study articles. Identify additional clinical data analysis in collaboration with the statistics team and subsequently submit and present the data in scientific forums.

Eligibility Criteria for the Non-Clinical Job:

  • Educational Qualification: MBBS +MD (Pharmacology)
  • Experience: 1 -2 years of previous work experience.

Required Skills for the Non-Clinical Job:

  • MD (Pharmacology) or other relevant medical qualification with 1-2 years of relevant experience or fresher.
  • Experience working in the clinical science domain in different capacities, as a medical monitor for clinical trials and a medical expert for clinical development plans for products across therapies, is desirable.

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