Apply for Medical Writer Parexel job 2026. Check eligibility, remote opportunity, salary, and application process for pharma professionals in India.
Introduction
If you are looking to grow your career in medical writing, pharmacovigilance, and clinical documentation, this opportunity from Parexel offers an excellent platform. The company is hiring skilled professionals for Medical Writer I and II roles, providing exposure to global clinical research projects. This role is ideal for candidates who want to work remotely while contributing to drug safety and regulatory documentation.
Job Overview
| Particulars | Details |
|---|---|
| Job Title | Medical Writer I / Medical Writer II |
| Company Name | Parexel |
| Location | Hyderabad (Remote – India) |
| Employment Type | Full-Time |
| Department | Medical Writing / Pharmacovigilance |
| Experience Required | Relevant experience preferred |
| Education | Life Sciences / Pharmacy / Biomedical Sciences |
| Salary | As per company norms |
Company Overview
Parexel is a globally recognized Clinical Research Organization (CRO) that supports pharmaceutical and biotechnology companies in clinical trials, regulatory consulting, and market access. Known for its patient-focused approach, Parexel plays a key role in bringing innovative therapies to market while maintaining high standards in safety and compliance.
Job Location & Employment Type
This is a remote job opportunity based in Hyderabad, allowing professionals across India to work in a flexible and collaborative environment. The role is full-time and part of Parexel’s global operations.
Open Positions / Department Details
Parexel is hiring for Medical Writer I and Medical Writer II positions within its Pharmacovigilance and Regulatory Writing team. These roles focus on safety reporting, clinical documentation, and regulatory submissions.
Key Roles & Responsibilities
Aggregate Report Writing & Safety Documentation
- Prepare and update Risk Management Plans (RMPs) and core safety documents
- Develop aggregate reports such as PSUR, PBRER, DSUR, PADER, and safety evaluation reports
- Ensure compliance with regulatory guidelines and SOPs
- Perform quality checks and ensure data accuracy across reports
Literature Review & Epidemiology
- Conduct systematic literature reviews for safety data
- Analyze epidemiological data such as incidence and prevalence
- Develop strategies for literature searches related to safety reports
Clinical Study Narratives
- Write clear and accurate patient narratives based on clinical and safety data
- Collaborate with study teams to ensure consistency and quality
- Perform narrative quality checks and formatting
Signal Detection & Risk Evaluation
- Perform signal detection using multiple data sources
- Analyze safety signals and contribute to risk assessment
- Participate in signal management activities and review meetings
General Responsibilities
- Maintain knowledge of global drug safety regulations
- Coordinate with cross-functional teams and stakeholders
- Ensure timely delivery of high-quality documents
- Support audits, inspections, and training initiatives
- Mentor junior team members (for higher roles)
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, or related field
- Degrees in Medicine, Nursing, or Physiotherapy are an added advantage
Experience
- Experience in medical writing, pharmacovigilance, or regulatory affairs is preferred
- Freshers with strong knowledge may be considered for entry-level roles
Skills Required
- Strong analytical and problem-solving abilities
- Excellent written and verbal communication skills
- Knowledge of medical terminology and clinical research processes
- Ability to work with MS Office tools and web-based applications
- Strong attention to detail and organizational skills
- Ability to manage multiple projects and deadlines
- Team collaboration and client-focused mindset
Salary & Benefits
- Salary: As per company norms
- Remote working flexibility
- Opportunity to work on global clinical projects
- Career growth in medical writing and pharmacovigilance
- Exposure to international regulatory standards
Selection Process
The hiring process typically includes:
- Resume screening
- HR interview
- Technical assessment or writing test
- Final interview
How to Apply
Candidates interested in this Medical Writer I / Medical Writer II at Parexel 2026 opportunity can apply online through the official Parexel careers portal. Ensure your CV highlights your experience in medical writing, pharmacovigilance, or clinical research.
Important Dates
- Application Deadline: April 10, 2026
Why Apply for This Job?
This Medical Writer I / Medical Writer II at Parexel role offers a strong foundation for professionals aiming to build a career in clinical research and regulatory writing. The opportunity to work remotely adds flexibility, while the exposure to global projects enhances your professional growth.
Parexel provides a collaborative work environment where employees contribute to meaningful healthcare advancements. You will gain hands-on experience in safety reporting, clinical documentation, and regulatory processes, which are highly valuable in the pharmaceutical industry.
FAQs
1. What is the focus keyword for this job?
The focus keyword is “Medical Writer Parexel”.
2. Is this job fully remote?
Yes, this is a remote role based in India, with Hyderabad as the primary location.
3. What experience is required?
Relevant experience in medical writing or pharmacovigilance is preferred, but entry-level candidates may also apply.
4. What skills are important for this role?
Strong writing skills, knowledge of medical terminology, and understanding of regulatory processes are essential.
5. How can I apply for this job?
You can apply online through Parexel’s official careers website.
Conclusion
The Medical Writer I / Medical Writer II at Parexel is an excellent opportunity for candidates looking to establish or grow their career in medical writing and drug safety. With remote flexibility, global exposure, and strong learning opportunities, this role is highly suitable for pharma and life sciences professionals. Apply before the deadline to secure your position.
Disclaimer
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