Novartis Hiring Clinical Scientific Expert
Posted inHyderabad

Novartis Hiring Clinical Scientific Expert

Additional InformationQualification : Master's, PharmD, M.Pharma, PhD, MBBS, BDS, MD strongly preferable. Fluent English (oral and written). Experience : >1 year experience.Job ID : REQ-10020654Location : HyderabadIndustry Type : Pharma /…
Syngene Hiring Junior Executive
Posted inHyderabad

Syngene Hiring Junior Executive

Exp- 0-3 Years Qualification- Bsc or Relevant (Preferably in Chemistry) Mode Of interview- Face to face Should have Knowledge of SAP MM- Module Good Documentation and SDS Management Must have…
Lee Pharma- R&D Department
Posted inHyderabad

Lee Pharma- R&D Department

Qualification- B.Sc/M.Sc. Exp.- 0 to 5 Years Location- Hyderabad (Kazipally) Mode of interview- Face to Face Need Male Candidates Only Interested Candidates share your Resume to talentaquisition@leepharma.com
Posted inBangalore Hyderabad

Parexel Hiring Medical Writer II

Knowledge and Experience: Relevant experience is desirable in Regulatory/ Pharmacovigilance or related field. Good knowledge of medical terminologies Education: Science/Medicine degree: The minimum qualification required would be a university degree…
Posted inBangalore Hyderabad

Parexel Hiring Clinical data Analyst II

Education:• Bachelor’s degree and / or other medical qualifications or relevant industry experience. Location: Only office Based- Bengaluru/Hyderabad Knowledge and Experience:• Strong technical aptitude with awareness/potential prior experience in Microsoft…
Posted inHyderabad

Arcolab Hiring Pharmacovigilance Associate

Walk in InterviewDate : 28th September, 2024Time : 9:00 AM onwardsVenue : 10th Floor, Building No 10, Raheja Mindspace, Hitech City, Madhapur, Hyderabad.Share the CV's with dev.kiran@arcolab.comOnly shortlisted candidates will…
Novartis Hiring for Regulatory Coordinator
Posted inHyderabad

Novartis Hiring for Regulatory Coordinator

Regulatory Coordinator Job ID REQ-10022239 Sep 16, 2024 India Summary -Contributes and support the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Supports all…