TransPerfect hiring Project Coordinator Pharmacovigilance
- Project Coordinator PV Vacancy – Pune
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Qualifications
- Desired Skills and Experience
- Relevant Educational Background
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- Is this a work-from-home position?
- Does this role require pharmacovigilance experience?
- What type of projects will I work on?
- How do I apply for this job?
- Summary Table
Project Coordinator PV Vacancy – Pune
TransPerfect hiring Project Coordinator Pharmacovigilance in Pune. Bachelor degree eligible. Full-time on-site vacancy. Apply now.
TransPerfect is inviting applications for the role of Project Coordinator – Pharmacovigilance (PV) Solutions at its Pune location. This opportunity is ideal for graduates seeking to build a stable and long-term career in pharmacovigilance, drug safety operations, and healthcare project management. The role offers hands-on exposure to literature monitoring projects, global healthcare clients, and regulatory-driven workflows within a structured professional environment.
Company Overview
TransPerfect is a globally established provider of language, technology, and business solutions, supporting leading pharmaceutical, biotechnology, clinical research, and healthcare organizations worldwide. The company plays a key role in regulatory submissions, pharmacovigilance services, clinical documentation, and post-marketing safety operations.
With a strong reputation in pharmacovigilance and life sciences solutions, TransPerfect supports global drug safety activities by ensuring accuracy, compliance, and operational excellence. The organization follows international regulatory standards and Good Pharmacovigilance Practices, making it a trusted partner for healthcare and pharmaceutical companies.
Job Role & Responsibilities
The Project Coordinator, Pharmacovigilance (PV) Solutions will handle day-to-day administrative and coordination tasks for literature monitoring and non-linguistic PV projects. The role supports the Production and Project Management teams to ensure timely delivery, compliance with regulatory standards, and consistent service quality.
Key Responsibilities
- Manage administrative components of pharmacovigilance literature monitoring projects
- Coordinate file transfers, internal tracking, and client deliveries
- Monitor project timelines and communicate progress to internal stakeholders
- Ensure strict adherence to client deadlines and quality benchmarks
- Implement and support Good Pharmacovigilance Practices (GVP) across projects
- Maintain Good Documentation Practice (GDP) standards in all project records
- Perform internal checks and balances to ensure process compliance
- Collaborate with cross-functional teams to resolve project-related issues
- Complete additional responsibilities assigned by managers or supervisors
This role contributes directly to global drug safety and regulatory compliance by supporting accurate and timely pharmacovigilance operations.
Eligibility / Qualifications
Required Qualifications
- Minimum Bachelor’s degree in any discipline
- Strong written and spoken English communication skills
- Proficiency in Microsoft Word, Excel, and Outlook
- Ability to adapt and work across multiple technology platforms
- Strong problem-solving and critical-thinking skills
- High attention to detail for regulatory-compliant deliverables
- Excellent organizational and time-management abilities
Desired Skills and Experience
- Ability to multitask in a fast-paced pharmacovigilance environment
- Comfortable working with global and cross-cultural teams
- Strong interpersonal and professional communication skills
- Ability to work independently and collaboratively
- Proactive mindset with a commitment to service quality
Relevant Educational Background
B.Pharmacy, M.Pharmacy, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Chemistry, B.Sc Nursing, M.Sc Life Sciences, M.Sc Biotechnology, M.Sc Pharmacology, Bachelor’s Degree in Science, Pharmacy, Life Sciences, Healthcare Management
Location & Salary
- Job Location: Pune, Maharashtra (On-site)
- Employment Type: Full-time, Permanent
- Department: Project Management – Pharmacovigilance Solutions
- Salary: As per industry standards and candidate experience
Compensation is competitive and aligned with current pharmacovigilance and healthcare project management market benchmarks.
Application Process
Eligible candidates can apply online through the official TransPerfect careers portal using the link below:
- Apply here: https://transperfect.recruitee.com/o/project-coordinator-pharmacovigilance-pv-solutions-pune
Candidates are encouraged to apply early, as applications are reviewed on a rolling basis.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Yes. Graduates with strong communication skills and interest in pharmacovigilance or healthcare project coordination can apply.
Is this a work-from-home position?
No. This is a full-time on-site role based in Pune.
Does this role require pharmacovigilance experience?
Prior pharmacovigilance experience is not mandatory, but knowledge of life sciences or healthcare processes is an advantage.
What type of projects will I work on?
You will support pharmacovigilance literature monitoring and non-linguistic PV projects for global healthcare clients.
How do I apply for this job?
Applications must be submitted through the official TransPerfect careers portal using the provided link
Summary Table
| Category | Details |
|---|---|
| Company | TransPerfect |
| Vacancies | Project Coordinator – Pharmacovigilance (PV) Solutions |
| Required Education | Bachelor’s Degree, B.Pharmacy, M.Pharmacy, Pharm.D, B.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Chemistry, Nursing |
| Experience | Freshers and Experienced Candidates |
To apply for this job please visit transperfect.recruitee.com.
