4 Veevarim Jobs

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8.0 - 12.0 years

0 Lacs

ranchi, jharkhand

On-site

As an experienced candidate with 8-12 years of experience, you will be responsible for the following key roles and responsibilities: - Familiarity with Pharmacovigilance Risk Management Plan (RMP) processes - Proficiency in Pharmacovigilance Periodic Safety Reports (PSR) processes - Ability to translate business requirements into technical specifications - Previous experience working with Top-30 Pharma companies - Cross-functional experience in safety, pharmacovigilance, and regulatory affairs - Good to have experience with Veeva.RIM - Good to have experience with Feith Orbit platform - Strong organizational skills and excellent verbal and written communication abilities If you are intereste...

Posted 1 day ago

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8.0 - 12.0 years

0 Lacs

ranchi, jharkhand

On-site

You have 8-12 years of experience and are looking for a permanent job opportunity. Your roles and responsibilities will include: - Experience in interface development and design. - Proficiency in Informatica. - Strong background in Oracle PL/SQL. - Familiarity with regulatory information management systems (RIMS). - Knowledge of IDMP (identification of medicinal products) standard. - Experience working in GxP environments, particularly in computer system validation. - Optional experience with ArisGlobal Total Safety suite (ARIS, LSMV). - Optional familiarity with Veeva.RIM. If you are interested in this position, please send your updated resumes to connect@datakaar.com.,

Posted 1 week ago

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8.0 - 12.0 years

0 Lacs

ranchi, jharkhand

On-site

You should have a minimum of 8 to 12 years of experience in interface development and design, Informatica, Oracle PL/SQL, regulatory information management systems (RIMS), and familiarity with the IDMP standard. Additionally, experience in GxP environments for computer system validation is required. Knowledge of ArisGlobal Total Safety suite (ARIS, LSMV) and Veeva.RIM would be a plus. This is a permanent position. If you meet these qualifications, please submit your updated resume to connect@datakaar.com.,

Posted 2 months ago

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8.0 - 12.0 years

0 Lacs

ranchi, jharkhand

On-site

You should have 8-12 years of experience in Pharmacovigilance, with familiarity in Pharmacovigilance Risk Management Plan (RMP) processes and Pharmacovigilance Periodic Safety Reports (PSR) processes. You should also have experience in translating business requirements into technical specifications and have worked with Top-30 Pharma companies. Cross-functional experience in safety, pharmacovigilance, and regulatory affairs is desired. Experience with Veeva.RIM and Feith Orbit platform is a plus. Strong organizational and verbal/written communication skills are essential for this role. If you meet the above criteria, please share your updated resume with us at connect@datakaar.com.,

Posted 3 months ago

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