Parexel is hiring for Medical Writer I / Medical Writer II – Patient Safety under its Medical Affairs function. The positions are available across Hyderabad, Bengaluru, Mohali and remote locations in India.
These roles focus on pharmacovigilance, medical writing and safety communications. Selected professionals will work on regulatory safety documents, aggregate reports, signal detection, safety data analysis, literature reviews and Risk Management Plans while collaborating with internal teams and external clients.
Parexel Medical Writer Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Parexel |
| Job Title | Medical Writer I / Medical Writer II |
| Job ID | R0000046349 |
| Department | Medical Affairs |
| Primary Location | Hyderabad, India |
| Additional Locations | Bengaluru, Mohali, Remote – India |
| Medical Writer I Experience | 2+ years |
| Medical Writer II Experience | 4+ years |
| Qualification | Degree in Life Sciences, Health Sciences or Biomedical Sciences |
| Domain | Pharmacovigilance / Patient Safety / Medical Writing |
| Key Skills | Scientific Writing, Signal Detection, Safety Data Analysis, Regulatory Writing |
| Salary/CTC | Not specified |
About Parexel
Parexel is a global clinical development organization working with biopharmaceutical companies and research organizations across the life sciences sector. Its activities cover clinical development, consulting and other services supporting the development of new therapies.
About the Medical Writer I / II – Patient Safety Role
The Medical Writer will support pharmacovigilance and patient safety activities by preparing scientifically accurate and regulatory-compliant documents.
The position involves analyzing safety information, preparing aggregate safety reports, conducting signal detection and evaluation, reviewing scientific literature and maintaining documentation required for regulatory and inspection readiness.
The role can also involve direct interaction with clients and collaboration with cross-functional teams.
Key Responsibilities
Regulatory Safety Writing
The selected candidate will contribute to the preparation and development of scheduled and ad-hoc safety documents, including:
- Periodic Safety Update Reports (PSURs)
- Periodic Benefit-Risk Evaluation Reports (PBRERs)
- Development Safety Update Reports (DSURs)
- Other regulatory safety documents
- Drug Safety Reports (DSRs)
- Signal Evaluation Reports (SERs)
- Risk Management Plans (RMPs) and related documentation
The writer will be expected to ensure that safety documents are scientifically accurate, clearly written and prepared within applicable timelines.
Signal Detection and Safety Data Analysis
Responsibilities include:
- Conducting independent signal detection activities.
- Reviewing safety information from multiple sources.
- Analyzing information from safety databases, clinical data, scientific literature and regulatory sources.
- Applying quantitative and qualitative approaches to identify potential safety signals.
- Preparing evidence-based signal assessments.
- Reviewing emerging safety trends.
- Supporting epidemiological and safety evaluations when required.
- Maintaining signal tracking records and logs.
- Identifying discrepancies between safety data sources and supporting their resolution.
Literature Review
The role includes systematic literature searches and reviews to support pharmacovigilance activities.
The candidate may evaluate published information to identify relevant safety findings, emerging trends and evidence needed for signal assessments and regulatory safety documents.
Risk Management Documentation
The Medical Writer will also support the preparation and updating of Risk Management Plans (RMPs) and related documents.
These activities require alignment between available safety information and applicable regulatory expectations across different therapeutic areas.
Client and Stakeholder Management
The role involves communication with internal stakeholders and clients.
Responsibilities may include:
- Responding independently to routine client queries.
- Escalating complex issues to the appropriate stakeholders.
- Providing regular project updates.
- Understanding client-specific requirements.
- Participating in document review and discussion cycles.
- Working collaboratively with cross-functional teams.
- Supporting delivery of high-quality safety documents.
Documentation and Inspection Readiness
Maintaining complete and accurate documentation is an important part of the role.
The selected candidate will:
- Maintain audit-ready records.
- Properly archive source documents and supporting materials.
- Support inspection-readiness activities.
- Follow applicable company procedures and regulatory requirements.
- Maintain data integrity across safety-related deliverables.
Additional Responsibilities for Medical Writer II
Medical Writer II professionals will have additional responsibilities involving leadership and mentoring.
These may include:
- Mentoring junior team members.
- Providing technical and professional feedback.
- Supporting the development of junior writers.
- Leading complex client discussions.
- Coordinating multi-stakeholder document review cycles.
- Contributing to process improvement initiatives.
- Supporting more complex safety writing and assessment activities.
Educational Qualification
Candidates should have a university degree in a relevant Life Sciences, Health Sciences or Biomedical Sciences discipline.
Relevant backgrounds may include:
- Pharmacy
- Microbiology
- Biochemistry
- Biotechnology
- Biophysics
- Dentistry
- Physiotherapy
- Other relevant Life Sciences or Biomedical disciplines
An equivalent combination of education, training and relevant work experience may also be considered.
Experience Requirements
The experience requirement differs according to the position:
Medical Writer I
Candidates should have 2 or more years of experience in:
- Pharmacovigilance
- Medical writing
- Patient safety
- Healthcare
- A related field
Medical Writer II
Candidates should have 4 or more years of relevant experience in pharmacovigilance, medical writing or a related field.
Medical Writer II candidates should also be capable of handling more complex assignments, mentoring junior professionals and supporting client discussions.
Required Skills and Knowledge
Candidates should have a good understanding of:
- Pharmacovigilance principles
- Global pharmacovigilance regulations
- Medical terminology
- Safety-related concepts
- Scientific writing
- Safety data interpretation
- Signal detection and evaluation
- Regulatory safety documentation
- Literature review
Technical proficiency should include:
- Medical writing tools
- Microsoft Office applications
- Pharmacovigilance databases
- MedDRA
- WHO-DD coding dictionaries
Strong analytical thinking and problem-solving abilities are important for interpreting complex safety information and developing clear, evidence-based conclusions.
Preferred Qualifications
Parexel also identifies the following as desirable:
- Previous pharmacovigilance or safety assessment experience
- Clinical experience in a hospital environment
- Direct clinical research experience
- Knowledge of specific therapeutic areas or product types
- Familiarity with pharmacovigilance systems
- Experience with regulatory submission processes across multiple regions
Key Professional Skills
The ideal candidate should demonstrate:
- Strong scientific writing ability
- Analytical thinking
- Attention to detail
- Problem-solving skills
- Clear written and verbal communication
- Strong organization
- Effective time management
- Ability to prioritize multiple projects
- Client-focused approach
- Ability to work collaboratively
- Commitment to quality and compliance
Work Location and Work Arrangement
The primary location for the vacancy is Hyderabad, India.
Additional locations listed by Parexel include:
- Bengaluru, India
- Mohali, India
- Remote, India
The vacancy therefore provides flexibility across different work arrangements, subject to the specific position and company requirements.
Salary and CTC
Parexel has not specified the salary or CTC for the Medical Writer I / Medical Writer II position in the provided job information.
Candidates should refer to the official recruitment communication for compensation details.
Selection Process
The detailed selection process has not been specified in the provided vacancy information. Candidates should follow the recruitment instructions provided by Parexel during the hiring process.
How to Apply for Parexel Medical Writer Recruitment 2026
Interested and eligible candidates can submit their application through the official Parexel careers portal.
Candidates should review the requirements for the appropriate level before submitting their application.
Important Details Before Applying
- Company: Parexel
- Position: Medical Writer I / Medical Writer II – Patient Safety
- Job ID: R0000046349
- Primary Location: Hyderabad
- Other Locations: Bengaluru, Mohali and Remote – India
- Department: Medical Affairs
- Medical Writer I: 2+ years relevant experience
- Medical Writer II: 4+ years relevant experience
- Qualification: Relevant Life Sciences, Health or Biomedical Sciences degree
- Core Domain: Pharmacovigilance and Patient Safety
- Salary: Not specified
- Application: Online through the official Parexel careers portal
Frequently Asked Questions
1. What position is Parexel hiring for?
Parexel is hiring for Medical Writer I / Medical Writer II – Patient Safety.
2. What is the job ID?
The job ID is R0000046349.
3. Where are these positions available?
The primary location is Hyderabad, with additional locations in Bengaluru, Mohali and Remote – India.
4. How much experience is required for Medical Writer I?
Medical Writer I requires 2+ years of experience in pharmacovigilance, medical writing or a related field.
5. How much experience is required for Medical Writer II?
Medical Writer II requires 4+ years of relevant experience.
6. What educational qualification is required?
A degree in Life Sciences, Health Sciences or Biomedical Sciences is required or preferred, depending on the applicable qualification pathway.
7. Is Pharmacy an eligible educational background?
Yes. Pharmacy is specifically listed among the relevant educational backgrounds.
8. What are the main responsibilities?
The role includes regulatory safety writing, aggregate safety reports, signal detection, signal evaluation, literature reviews, Risk Management Plans and safety documentation.
9. Which pharmacovigilance tools or standards are relevant?
The role mentions pharmacovigilance databases and coding dictionaries including MedDRA and WHO-DD, along with medical writing tools and MS Office.
10. Is Medical Writer II responsible for mentoring?
Yes. Medical Writer II professionals may mentor junior team members, provide feedback and lead complex client and document-review activities.
11. Is the salary mentioned?
No. The provided vacancy does not specify a salary or CTC.
12. Where can candidates apply?
Candidates can apply through the official Parexel careers link provided in the How to Apply section.
Important Note
Job availability, eligibility criteria, responsibilities, work arrangements and other recruitment conditions may change. Candidates should verify the latest information on the official Parexel careers portal before submitting their application.