- Dear Candidate,
Looking for candidates with 2-6 yrs of experience on
Safety Draft Exchange Agreements, Pharmacovigilance Agreements, Draft and negotiation of pharma or PV agreements, Attention to detail, Post Marketing/Agreements and Excellent Communication skills.
Interested candidates can share there resume to Kavya.l2@iqvia.com or Shivangi.gaur@iqvia.com.
Walk-In Details:
Date: 2-Mar-19
Venue - IQVIA
G Corp, 12th & 13th,
Ghodbunder Rd, Sai Nagar,
G Corp, 12th & 13th,
Ghodbunder Rd, Sai Nagar,
Kasarvadavali,
Thane West,
Thane West,
Maharashtra 400615
Job Description
PURPOSE
Under general supervision, develop and prepare pharmacovigilance agreements for assigned customers.
RESPONSIBILITIES
Work closely with project teams to determine appropriate terms and conditions of safety agreements
Develop and prepare safety agreements
Prepare and maintain PSMFs for small/mid-size companies
Act as primary customer interface on small to mid-size projects
Support senior team members on medium to larger customers / projects
Assist in the negotiation of safety agreement text using approved process and templates
Oversee finalization and distribution of documents
Update and maintain safety agreement databases and files
All responsibilities are essential job functions unless noted as nonessential (N).
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of applicable global, regional and local clinical research regulatory requirement; i.e. Good Pharmacovigilance Practice (GVP) and International Conference on Harmonization (ICH) guidelines, Quintiles Standard Operating Procedures.
Good knowledge of Lifecycle Safety processes;
Excellent attention to detail and accuracy and maintain consistently high quality standards.
Excellent written and verbal communication skills.
Ability to work effectively on multiple projects simultaneously. Organize own workload and effectively time manage competing priorities.
Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Regards,
Kavya
Job Description
PURPOSE
Under general supervision, develop and prepare pharmacovigilance agreements for assigned customers.
RESPONSIBILITIES
Work closely with project teams to determine appropriate terms and conditions of safety agreements
Develop and prepare safety agreements
Prepare and maintain PSMFs for small/mid-size companies
Act as primary customer interface on small to mid-size projects
Support senior team members on medium to larger customers / projects
Assist in the negotiation of safety agreement text using approved process and templates
Oversee finalization and distribution of documents
Update and maintain safety agreement databases and files
All responsibilities are essential job functions unless noted as nonessential (N).
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of applicable global, regional and local clinical research regulatory requirement; i.e. Good Pharmacovigilance Practice (GVP) and International Conference on Harmonization (ICH) guidelines, Quintiles Standard Operating Procedures.
Good knowledge of Lifecycle Safety processes;
Excellent attention to detail and accuracy and maintain consistently high quality standards.
Excellent written and verbal communication skills.
Ability to work effectively on multiple projects simultaneously. Organize own workload and effectively time manage competing priorities.
Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Regards,
Kavya
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