September 2026

Knowledge of Instruments like HPLC, UPLC, GC, UV, AMV, Knowledge of HPLC / AMV as reviewer.

As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.

Collaborate with lab staff to gather study requirements, test article information, and study design details necessary for study initiation, laboratory assignment, and resource planning.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

As the sole CRA Manager in India, this role presents an opportunity to build and lead your own team and to take your career to the next level as you work closely with the Senior Director of Clinical Monitoring.

Manage and deliver a wide range of medical writing tasks to a consistently high standard and take the role of Clinical Reporting Project Lead or Medical Writing Lead.

Bachelors degree in pharmacy or Life Sciences related field with 4-7 years of pharmacovigilance experience. 

M.Pharm, PharmD, or PhD (Pharmaceutical/Life Sciences). MBA will be an added advantage. Johnson & Johnson

Bachelors or Masters degree in Pharmaceutical Sciences, Life Sciences, Chemistry, Engineering, Sciences, or a related discipline