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Project Coordinator, Pharmacovigilance (Pv) Solutions | Pune

Transperfect
Transperfect
0-2 years
preferred by company
10 Jan. 26, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Project Coordinator – Pharmacovigilance (PV) Solutions

Location: Pune, Maharashtra, India
Work Mode: On-site
Function: Project Management | Pharmacovigilance
Employment Type: Full-Time


About the Company

TransPerfect is a global leader in language, content, and life sciences solutions, supporting pharmaceutical, biotech, and medical device organizations worldwide. Through its Pharmacovigilance Solutions division, TransPerfect delivers compliant, high-quality safety and literature monitoring services aligned with global regulatory standards.


Job Overview

The Project Coordinator – Pharmacovigilance (PV) Solutions will support the operational and administrative execution of pharmacovigilance literature monitoring and non-linguistic safety projects. This role is critical to ensuring on-time delivery, process compliance, and high-quality outputs across client programs. The position works closely with the Production and PV teams and is ideal for professionals seeking to build a career in pharmacovigilance project coordination.


Key Responsibilities

  • Manage day-to-day administrative activities for non-linguistic pharmacovigilance projects, including literature monitoring support

  • Coordinate file transfers, internal quality checks, and client deliverables in accordance with project timelines

  • Track project progress and proactively communicate status updates to internal stakeholders

  • Ensure strict adherence to client deadlines and internal service level agreements

  • Apply Good Pharmacovigilance Practices (GVP) and Good Documentation Practices (GDP) across all assigned projects

  • Support process compliance and continuous improvement initiatives within the PV Production team

  • Perform additional tasks and responsibilities as assigned by the manager or supervisor


Required Qualifications & Experience

  • Education: Bachelor’s degree in any discipline (Life Sciences preferred)

  • Experience Required: 0–2 years of experience in project coordination, pharmacovigilance support, clinical operations, or related administrative roles


Required Skills & Competencies

  • Excellent written and verbal communication skills in English

  • Strong proficiency in Microsoft Office tools (Word, Excel, Outlook)

  • Ability to quickly learn and adapt to new technologies and systems

  • Strong problem-solving and analytical skills

  • High attention to detail with a commitment to quality and accuracy

  • Excellent organizational and time-management skills


Preferred Skills & Attributes

  • Ability to manage multiple tasks in a fast-paced, deadline-driven environment

  • Experience working with cross-functional and multicultural teams

  • Strong interpersonal skills with the ability to build effective working relationships

  • Ability to work independently as well as collaboratively within a team

  • Proactive mindset with a strong customer-service orientation


Why Join TransPerfect

  • Opportunity to work on global pharmacovigilance and safety programs

  • Exposure to regulated PV operations and literature monitoring projects

  • Collaborative and inclusive work environment

  • Career growth opportunities within life sciences project management

  • Hands-on experience supporting compliant, patient-focused safety solutions


Apply now on thepharmadaily.com to build your career in Pharmacovigilance Project Coordination with a global life sciences organization.