Experience:- 1-7 yrs Location:- Ahmedabad Education Qualification:- Graduate degree holder in any medical discipline Job Description:- Data Entry and Quality Check of ICSRs in pharmacovigilance database Preparation of PSURs per the Regulations and SOPs Understand product characteristics ...
innovative medical content products by leveraging on the depth of scientific content Adhering to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards, requirements, and policies
Controlling/reducing the cost of content development, cycle times, and error rates in projects Developing innovative medical content products by leveraging on the depth of scientific content Adhering to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory
Candidate MUST be BSc Nursing Graduate. He could have work experience in Hospitals - Staff Nurse / Pharmacovigilance / Toxicology / Clincal studies / Clinical Trials Duties and Responsibilities: SME review of section 4(First Aid Phrase) of MSDS Work in SAP R/3 and NEA (ECC) to complete Section 4
have been in a customer facing role for >4 years - Willing to work in shifts Industry Pharma / Biotech / Clinical Research functional Area Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology Job Role Clinical Research Manager Keyword pharmacovigilance drug safety team management
Training- Advanced PG Diploma in Pharmacovigilance/Drug Safety in Oracle Argus Safety Database with Practical Hands on Training - Project Experience Certification • Online Training-Pharmacovigilance/Drug Safety in Oracle Argus Safety Database with practical Hands on Training with Project • Online