Experience: 8 - 12 years. Job type: Permanent. Roles and Responsibility: Familiar with Pharmacovigilance Risk Management Plan (RMP) processes Familiar with Pharmacovigilance Periodic Safety Reports (PSR) processes Experience in transfer of business requirements into technical specifications Experience with Top-30 Pharma companies Cross-functional experience safety / pharmacovigilance and regulatory affairs Good to have experience with Veeva.RIM Good to have experience with Feith Orbit platform Strong organization and verbal/written communication skills Please share your updated resumes on connect@datakaar.com
Experience: 8 - 12 years. Job type: Permanent. Roles and Responsibility: Experience in interface development and design. Experience in Informatica. Experience in Oracle PL/SQL. Experience with regulatory information management systems (RIMS). Familiar with IDMP (identification of medicinal products) standard. Experience in GxP environments (computer system validation). Experience with ArisGlobal Total Safety suite (ARIS, LSMV) - optional. Familiar with Veeva.RIM - optional. Please share your updated resumes on connect@datakaar.com
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.,
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.,