Apply for Parexel Medical Writer I II remote job in India. Check eligibility, pharmacovigilance writing responsibilities, and application process details.
Introduction
If you are aiming to build a strong career in pharmacovigilance, medical writing, and drug safety reporting, this opportunity is highly valuable. A globally reputed CRO is hiring Medical Writers who can contribute to safety documentation, aggregate reports, and clinical narratives. This role offers remote flexibility along with exposure to international regulatory standards and safety reporting practices.
Company Overview
Parexel is a globally established Contract Research Organization (CRO) providing clinical development, regulatory consulting, and medical writing services to pharmaceutical and biotechnology companies. With operations across multiple countries, the organization supports the development of innovative therapies while maintaining high standards of quality and compliance.
Job Overview (Quick Details)
| Job Title | Medical Writer I / Medical Writer II |
|---|---|
| Company | Parexel |
| Location | India (Remote) |
| Employment Type | Full-Time |
| Department | Medical Sciences / Pharmacovigilance |
| Experience Required | Freshers to Experienced (Relevant experience preferred) |
| Education | Life Sciences / Medical Degree |
| Salary | As per company norms |
| Job ID | R0000037044 |
Job Location & Employment Type
- Location: Remote (India)
- Employment Type: Full-time
Open Positions / Department Details
- Department: Medical Writing & Drug Safety
- Role includes working on aggregate safety reports, clinical narratives, and signal detection activities
- Opportunity to collaborate with global pharmacovigilance teams
Key Roles & Responsibilities
Aggregate Safety Reports
- Prepare and update Risk Management Plans (RMPs) and related safety documents
- Work on periodic safety reports such as PSUR, PBRER, DSUR, and PADER
- Develop safety evaluation reports, clinical overviews, and risk-benefit assessments
- Perform literature review and epidemiological analysis for safety data inclusion
- Ensure consistency, accuracy, and regulatory compliance in all reports
- Handle line listings and identify discrepancies in safety data
Clinical Study Narratives
- Draft patient safety narratives based on clinical and safety databases
- Collaborate with study management teams for narrative development
- Review and refine narratives to ensure medical clarity and consistency
- Perform quality checks and ensure proper formatting and completeness
- Act as a point of contact for narrative-related queries
Signal Detection & Management
- Conduct signal detection activities using multiple data sources
- Perform qualitative and quantitative analysis of safety signals
- Support signal evaluation and reporting processes
- Participate in safety review meetings and discussions
General Responsibilities
- Maintain knowledge of drug safety profiles and regulatory requirements
- Ensure compliance with global pharmacovigilance guidelines
- Participate in audits, inspections, and training sessions
- Coordinate meetings, track action items, and follow up on deliverables
- Mentor junior team members when required
- Communicate effectively with internal teams and clients
- Support process improvements and quality initiatives
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, or related field
- Candidates with degrees in Medicine, Dentistry, Nursing, Physiotherapy, or related clinical fields will have an added advantage
Experience
- Freshers with strong academic background can apply
- Experience in pharmacovigilance, regulatory writing, or medical writing is preferred
- Prior exposure to safety reporting and aggregate reports is a plus
Skills Required
- Strong analytical and critical thinking abilities
- Excellent written and verbal communication skills
- Good understanding of medical terminology
- Ability to summarize complex medical data clearly
- Attention to detail and accuracy in documentation
- Ability to manage multiple tasks and deadlines
- Proficiency in MS Office tools (Word, Excel, PowerPoint)
- Familiarity with global safety reporting guidelines
- Strong teamwork and client-focused approach
Salary & Benefits
- Salary: As per company norms
- Additional benefits may include:
- Work-from-home flexibility
- Exposure to global pharmacovigilance projects
- Learning and development opportunities
- Career growth in medical writing and drug safety
Selection Process
The recruitment process typically includes:
- Application screening
- HR interview
- Technical/medical writing assessment
- Final interview round
How to Apply
- Candidates should apply through the official Parexel careers website
- Use Job ID: R0000037044 while searching
- Submit an updated resume highlighting relevant skills and experience
Important Dates
- Last Date to Apply: Not specified
Why Apply for This Pharma Job?
- Opportunity to work with a globally recognized CRO
- Gain expertise in pharmacovigilance and regulatory writing
- Exposure to international drug safety reporting standards
- Flexible remote work environment
- Strong career growth opportunities in medical writing domain
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Parexel or any recruiter. We do not charge any fees for job postings. Candidates are advised to verify all details through official sources before applying.
Final Call-to-Action
Interested candidates should apply as soon as possible to secure this opportunity and build a successful career in medical writing and pharmacovigilance.
