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Regulatory affairs

 

Clinical courses

 

Clinical research courses

  • Job requirement for Clinical Trial Registry Specialist at Lilly

    Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 140 years.  Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health.

    Post : Clinical Trial Registry Specialist

  • Job for Assistant Manager in Regulatory Affairs at Sandoz Private Limited

    At Novartis, we use science-based innovation to address some of society’s most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible.

    Post : Asst. Manager – Regulatory Affairs-API

  • Job for Consultant in Global Regulatory Affairs at Lilly

    Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 140 years.  Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health.

    Post : Consultant, Global Regulatory Affairs, CMC

  • Job for Manager in Regulatory Affairs at PAREXEL

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

    Post :  Manager Regulatory Affairs

  • Job for Drug Safety Associate at Parexel | Degree in Life Sciences, Pharmacy

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

    Post: Drug Safety Associate

  • Opportunity at Amgen as Regulatory Affairs Associate

    Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.

    Post : Regulatory Affairs Associate

  • Job for Master in Pharmacy in Regulatory Affairs at Johnson & Johnson

    Johnson & Johnson was founded more than 120 years ago on a revolutionary idea: Doctors and nurses should use sterile sutures, dressings and bandages to treat peoples’ wounds.  Johnson & Johnson is ranked by Fortune Magazine as the 3rd most Admired Pharmaceutical Company in the world with an outstanding product range as well as an extensive research base with a number of life saving original research molecules.

    Post : Manager, Regulatory Affairs

  • Job for Senior Manager- Regulatory CMC at MSD

    MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where MSD has codified its 125-year legacy. MSD’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

    MSD’s Regulatory Affairs division helps bring new medical advancements to the world by facilitating the communications and procedures that allow swift, organized compliance across regulatory agencies. As a team of energetic, results-driven individuals, we’re a global network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices, and solutions to the world on time, every time.

    Post : Sr. Manager- Regulatory CMC

  • Career for M.Pharm, B.Pharm as Regulatory Affairs Specialist at Medtronic

    This is a question we’ve asked ourselves over and over. It’s how we at Medtronic have made hearts beat stronger and longer. It’s how we’ve pushed the limits of what technology can do in and for the body. It’s how we will continue to alleviate pain, restore health and extend life. Rising costs, an aging population, and the burden of chronic disease impact us all. And no single entity in the healthcare system can solve these challenges alone. That’s why we’re stepping forward. That’s why we’re prepared to put the full power of our technologies, services, resources — and our people — to work with new partners, in new ways, to usher in a new era in healthcare.

    Post : Assoc Regulatory Affairs Spec

  • Multiple Job openings for M.Pharm, M.Sc in Etico Lifesciences Private Limited

    Etico is an ethical pharmaceutical company founded in 2016 and based out in Hyderabad, India. We are specialized in development of oncological and non-oncological parenteral dosage forms development and provide product development and technology transfer solutions to innovator and generic pharmaceutical companies worldwide.

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