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Clinical Research

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Clinical research courses

  • Interview for Pharma or Life Science Graduate at MPMMCC

    The  Tata Memorial Centre ( TMC) is a Comprehensive Cancer Centre with a mission to achieve the highest standards in patient care, cancer prevention, cancer research and professional development for oncology and allied disciplines.  TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India. TMC is affiliated to Homi Bhabha National Institute (HBNI).

  • Opportunity for M.Pharm, Pharm.D to Join Indian Pharmacopoeia Commission as Operations Director

    Indian Pharmacopoeia Commission (IPC) is an Autonomous Institution of the Ministry of Health and Family Welfare, Govt. of India. IPC is created to set standards of drugs in the country. Its basic function is to update regularly the standards of drugs commonly required for treatment of diseases prevailing in this region. It publishes official documents for improving Quality of Medicines by way of adding new and updating existing monographs in the form of Indian Pharmacopoeia (IP).

  • Work as Clinical Research Associate at Teva

    Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.

    Post : Clinical Research Associate I

  • DPSRU M.Pharm, M.S Pharm Recruitment - Research Scientist Post | Salary Rs. 56,000 pm plus HRA
    M.S. Pharm/ M.Pharm with specialization in Clinical Research/ Clinical Pharmacology / Pharmacology & Toxicology. Clinical Evaluation of Fibroblast Growth Factor FGF and Silver Nanoparticle AgNP Entrapped Gelatin, Gellan Hybrid Gels as Wound Dressings in Diabetic Foot Ulcer Patients
  • Vacancy for Clinical Trial Coordinator at MPMMCC
    Graduate in Life Science with Relevant Experience in Clinical Research. Post graduate degree in Life Science and Diploma in Clinical Research is desirable.
  • Indian Pharmacopoeia Commission Recruitment for M.Pharm, MSc as Materiovigilance Associate Post
    To organize national as well as international meetings/seminars, webinars, workshops, awareness programs, CMEs on medical devices for the awareness of healthcare professionals, medical device industries and consumers in order to promote the safety and efficacy of medical devices.
  • Opportunity for M.Pharm to Join Indian Pharmacopoeia Commission as Complaint Executive

    Indian Pharmacopoeia Commission (IPC) is an Autonomous Institution of the Ministry of Health and Family Welfare, Govt. of India. IPC is created to set standards of drugs in the country. Its basic function is to update regularly the standards of drugs commonly required for treatment of diseases prevailing in this region. It publishes official documents for improving Quality of Medicines by way of adding new and updating existing monographs in the form of Indian Pharmacopoeia (IP).

  • Job for Pharma and Life Sciences Candidates at Tata Memorial Centre

    The Tata Memorial Centre is a Comprehensive Cancer Centre with a mission to achieve the highest standards in patient care, cancer prevention, cancer research and professional development for oncology and allied disciplines. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India. TMC is affiliated to Homi Bhabha National Institute.

    Required for the post of Clinical Trial Co-ordinator on DAE-CTC Project (A/c No. 963) (Initially for a period of six months.) 

  • Public Health Foundation of India looking for Assistant Professor
    Lead and undertake teaching for on-campus and eLearning programs including mentorship of students for dissertations and internship activities. Assess and monitor student performance across modules for on-campus and eLearning programs.
  • Work as PV RA MW Coordinator at Thermo Fisher Scientific
    Provides critical support and coordination in the review of safety and regulatory publishing documents, ensuring timely and accurate processing upon receipt. Plays a key role in maintaining document quality by tracking safety and regulatory publishing data, ensuring seamless uploading into internal and/or external electronic trial master files.
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