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Pharm.D

GPAT courses

  • Job for M.Pharm or Doctoral Degree in Pharma at National Chemical Laboratory, Salary Rs. 42,000 pm

    Masters in Natural or Agricultural or Pharmaceutical Sciences, Animal Sciences OR Bachelors degree in Engineering or Technology or Medicine from a recognized University OR Doctoral Degree in Science, Pharma, MD, MS from a recognized University or equivalent
  • Opportunity for Pharm.D, M.Pharm, MSc as Clinical Trial Coordinator at MCC-PGIOSR
    Pharm.D, MPharm, BDS, MPH, MSc Biostatistics, MSc Clinical Research, MSc Nursing Or MSc Life Science, BTech Biotechnology with Post graduate Diploma in Clinical Research
  • Novo Nordisk Looking for Associate Global Scientific Advisor
    As an Associate Global Scientific Advisor, you will Provide timely, accurate and credible scientific and medical input for a variety of projects pertaining to scientific communication around Novo Nordisk’s products. Collaborate closely and communicate effectively with various cross-functional stakeholders including colleagues from the US affiliate, global medical affairs, and other functional areas. Engage in dialogue with Key Opinion Leaders (KOLs) in different settings with focus on medical and scientific information. Prepare presentations for Novo Nordisk standalone events and international medical congresses.
  • Job for M.Pharm or Pharm.D as Pharmacovigilance Associate at AIIMS
    Master degree in Pharmacy, Clinical Pharmacology, Pharmacy Practice, and Clinical Research. OR Pharm.D, MBBS, BDS from a recognised university, Institute. 
  • Opportunity for M.Pharm, MSc, Pharm.D as Senior Project Associate at NCL
    Membrane preparation and characterization. Prior experience of working in research laboratory, industry desired. Direct Sea Water Electrolysis by electrolyte engineering & by coupling electrolyser directly with FO module.
  • Job for Pharma and Life Sciences Candidates under DST sponsored SATHI Program at Banaras Hindu University
    Doctoral degree in Science, Engineering, Technology, Pharma, MD, MS from a recognized University or equivalent and experience in Research and Development in industrial and Academic institutions or science and technology organizations and scientific activities and services. To operate and maintain analytical and/or imaging Equipment such as Ion Chromatograph/ HRMS/ IRMS/ NMR/ photoacoustic imaging/confocal laser scanning microscopy/ ICPMS or related equipment and in interpreting their data.
  • Novo Nordisk Require Medical Writer - Ph.D, M.Pharm, Pharm.D Apply
    Performing medical writing tasks for trial and/or non-trial activities within clinical reporting including but not limited to preparation of Protocols, Clinical Trial Reports CTRs, Non-interventional study reports NSRs, Layperson Summary LPS, Investigator Brochure and Regulatory response documents. PhD, MSc, MPharm, PharmD
  • IISc Admission Notice for the Academic Year 2025-26
    The educational qualifications remain the same as for the regular candidates. Qualifying in one of the national entrance tests like CSIR-UGC NET for JRF, UGC-NET for JRF, DBT JRF, ICMR JRF, GATE, and NBHM is desirable but not mandatory. Further, the candidate should have completed two years of full-time employment in the current organization after completion of degree. The candidates must be officially sponsored by their employing organizations and compulsorily fill in an online application form and submit the printed version, in duplicate, on or before 07th April 2025.
  • Job as Associate Professor, Assistant Professor at Kota College of Pharmacy - Pharmaceutical Chemistry, Pharmaceutical Analysis, Quality Assurance, Pharmaceutics
    Pharmaceutical Chemistry, Pharmaceutical Analysis, Quality Assurance, Pharmaceutics; Kota College of Pharmacy emphasizes on the overall development of the students since last 18 Years. It aims at not only producing good pharmacist but also good and worthy citizens of the society.
  • TCS hiring Pharma candidates for Gandhinagar location, only experienced
    Looking for clinical Database Developer experience in eCRF build and edit checks build in Veeva studio; Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process. Providing support for the mapping and transformation of clinical data to CDISC SDTM standards. Work independently and accountable for study Data Management deliverables; Coordinate with Biostatistician, Clinical, Medical and local study team as applicable
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