Drug Regulatory Mumbai

Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Clinical Safety Manager to join our Clinical

Location: Delhi/Mumbai/Hyderabad Business Unit: CMR (Clinical, Medical, Regulatory and Pharmacovigilance) Are you passionate about what you are doing? Do you

About the job SANOFI CHC PURPOSE AND ASPIRATION At Sanofi CHC, we have one shared purpose - we work passionately, every day, to 'serve healthier, fuller lives.

Mobile Software Engineer II Contribute to the design and development of software across Android and iOS mobile applications under a disciplined product

Pharmacovigilance Associate Freshers Essential Duties and Responsibilities Collect and evaluate adverse event reports from various sources including healthcare

Location: Delhi/Mumbai/Hyderabad Business Unit: CMR (Clinical, Medical, Regulatory and Pharmacovigilance) Are you passionate about what you are doing? Do you

- Represent AbbVie Medical Affairs as subject matter expert Oncology and territory, provide scientific and technical leadership to ensure professional and

Catawba Research India is looking for an organized, flexible Clinical Research Associate to oversee clinical trials. Qualification: Bachelor’s Degree OR

Purpose: Formulation and process development using QbD paradigm to deliver products in a defined timeframe to meet product delivery goals for I&D.; Guide and

Location: Delhi/Mumbai/Hyderabad Business Unit: CMR (Clinical, Medical, Regulatory and Pharmacovigilance) Are you passionate about what you are doing? Do you

Position: Regulatory ExecutiveEligibility : M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory Affairs. Should have good knowledge of

Position: Regulatory ExecutiveJob Location: Vile Parle Mumbai: MaharashtraEligibility :M. Sc / B. Sc / M. Pharm / B. Pharm. Degree / Diploma in Regulatory

Skill : Medical Reviewer Qualification : MBBS/MD only (MCI Certification is not mandate**) Preferred Experience: Minimum of 1-5 years of experience in PV/

About the role Your responsibilities include, but are not limited to: • Lead and contribute to Clinical Data Standards definition, development, validation

CLIENT : is a leading healthcare organization providing services to the medical profession through the introduction of innovative molecules, information-based