Pharmacovigilance Associate- Fresher- Pharmacy/ Biotech/ Bioinformatic Gratisol Labs

0.0 - 1.0 years

2 - 3 Lacs

Hyderabad, Pune, Bengaluru

Work from Office

Perform triage & intake of ICSR received daily in ARGUS databases Should have hands On Experience On ARGUS Safety Database Should Have hands on Experience on MEDDRA Applicants Should Complete Certification in Pharmacoviiglance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Posted 3 months ago

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Walk In- Pharmacovigilance Associates - Freshers- Pharma/ Life Science Gratisol Labs

- 2 years

2 - 3 Lacs

Hyderabad

Work from Office

Posted 4 months ago

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Medical Writer - Medical Affairs Eli Lilly And Company

7 - 9 years

11 - 12 Lacs

Bengaluru

Work from Office

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position. EMS (Executive Medical Summary) Content Strategy and Execution: Document Preparation, Development and Finalization/Document Management Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing pro...

Posted 4 months ago

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Walk In - Pharmacovigilance Associate -Pharma / BDS / Life Sciences Gratisol Labs

3 - 5 years

3 - 4 Lacs

Hyderabad

Work from Office

We are currently hiring for DSA I role with a minimum of 3 to 5 years Of experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Knowledge In Aggregate Reporting is Must Required Candidate profile Require 3 to 5 years of pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT)

Posted 4 months ago

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Junior Drug Safety Associate - B pharm/M Pharm/ Pharm D/ Life Sciences Gratisol Labs

1 - 2 years

3 - 4 Lacs

Hyderabad, Pune, Bengaluru

Work from Office

We are currently hiring for DSA I role with a minimum of 1 year experience in Pharmacovigilance Perform triage & intake of ICSR received daily in ARGUS databases. Ensure data entry of ICSR in ARGUS Required Candidate profile A minimum of 1 year pharmacovigilance case processing experience. Responsible for coding events using MEDDRA Any Life Sciences(B pharm/M Pharm/ Pharm D, Life Sciences, Nursing, BDS, BPT) are Eligible

Posted 4 months ago

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Officer - Clinical Research/BA/BE Studies Medreich

4 - 5 years

4 - 5 Lacs

Bengaluru

Work from Office

Basic understanding of Clinical pharmacology, pharmacokinetics and toxicological aspects Review of literature and preparation of Biopharmaceutics review, Dissolution studies , Biowaiver/Bio strategy Basic understanding of bioequivalence studies for various regulatory agencies Review of study specific documents for BE studies (like study protocol, ICF,CRF, CSR, TMF) Monitoring & audit of clinical phases of Biostudies and Quality management system Co-ordination with CROs for execution of Pilot and Pivotal bioequivalence studies. Co-ordination with internal departments for BE NOC/TL documents and project contracts/invoices. Management, receipt, logistics and shipment of study IMPs to CRO’s Subm...

Posted 4 months ago

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Clinical Pharmacist Hlg Memorial Hospital

1.0 - 5.0 years

1 - 2 Lacs

asansol

Work from Office

The pharmacist is responsible for preparing, dispensing, and managing medications as prescribed by physicians. They ensure the safe and effective use of pharmaceutical drugs and counsel patients on proper medication use, side effects.

Posted Date not available

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Walk In- Pharmacovigilance Associates - Freshers- Pharma/ Life Science Clininfotech

0.0 - 2.0 years

2 - 3 Lacs

hyderabad

Work from Office

Posted Date not available

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Global Scientific Communications Regulatory Writing Eli Lilly And Company

2.0 - 6.0 years

15 - 19 Lacs

bengaluru

Work from Office

Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. Conduct effective document initiation meeting to ensure authoring team alignment and understanding. Build scientific-based rationale that support the purpose of more complex and/or strategic documents. Ensure data are presented in a clear, complete, accurate, and concise manner. Ensure that key data, statements and conclusi...

Posted Date not available

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