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This role sits within Thermo Fisher's Clinical Data Management team, based in Bengaluru. As a Clinical Data Team Lead, you will act as the lead data manager for...

This role is based out of Chennai. You will be responsible for creating on-time pharmacovigilance reports. You will ensure that each PV report satisfies standar...

Based in Chennai this role is about keeping clinical trial data accurate and reliable. As a Clinical Validation Analyst, you will run checks to catch errors bef...

Accenture's Regulatory Services team will work closely on Life Sciences Regulatory Affairs. You are required to support submission tasks, which include formatti...

This role sits within the Post Market Surveillance Center of Excellence, based in Bangalore. As a Quality Specialist II, you will update and maintain approved P...

The Medical Copywriting Lead role is about making sure medical content is good, interesting and follows the rules of pharmaceutical marketing. They will make co...

This role sits within the Regulatory Affairs Operations team, based in Gurgaon. As a Specialist you will support internal reporting work tied to frameworks, lik...

This role sits within the Quality Control Lab, based in a global pharmaceutical manufacturing setup. As a Trainee Officer, you will carry out in process and fin...

This job offers services that match the CGMP rules and the Novartis Quality Management System. As a Quality Assurance Operations Specialist you will take charge...

This role sits within Masimos growing Regulatory Affairs team, based in Bengaluru. As a Regulatory Affairs Specialist you will support both international filing...

This role is based in Kolkata, within Abbott's Medical and Clinical Affairs team. As a Regional Medical Advisor, you will provide scientific and medical support...

This role supports the Medical Information team and senior management with day to day administrative work. As a Medical Information Assistant you will help make...

This job is part of an expanding pharmacovigilance team that focuses on drug safety. As a Senior Drug Safety Associate you will handle the process of dealing wi...

This job is part of an expanding medical writing team that helps with research projects. As a Senior Medical Writer you will. Check important clinical papers fr...

This role is part of the Smart Care team within Stryker's Regulatory Affairs group. As a Senior Specialist, you will support regulatory work across the full pro...

This specialist role sits within the Pharma Research and Development space focused on pharmacovigilance. As a Specialist you will support drug safety by managin...

This position belongs to the Regulatory Affairs team located in Gurgaon, India. As a Senior RA Specialist, you will handle activities for Baxter’s pharmaceutica...

This role is based in Sanofi’s Registries team, which's part of the General Medicines function in Hyderabad. Central Clinical Research Associate will be the poi...

This position is located in Hyderabad, within the Medical function of Sanofi, in Externally Sponsored Research. As Associate Project Manager, you will be respon...

This is a temporary role, a nine month contract, based on-site with the Patient Safety Operations team. As a Patient Safety Associate II or Specialist, you will...