Parexel is hiring for Medical Writer I and Medical Writer II – Patient Safety positions across multiple locations in India. The opportunities are available in Hyderabad, Bengaluru and Mohali, with remote options listed for Hyderabad and Mohali.
These positions are focused on pharmacovigilance, medical writing, safety signal management and regulatory safety documentation. Candidates with relevant life sciences or healthcare qualifications and experience in pharmacovigilance, medical writing or related fields can apply.
The experience requirement is 2+ years for Medical Writer I and 4+ years for Medical Writer II.
Parexel Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Parexel |
| Job Title | Medical Writer I / Medical Writer II – Patient Safety |
| Job Requisition ID | R0000046349 |
| Locations | Hyderabad, Bengaluru, Mohali |
| Remote Options | Hyderabad Remote / Mohali Remote |
| Medical Writer I Experience | 2+ Years |
| Medical Writer II Experience | 4+ Years |
| Qualification | Life Sciences / Health / Biomedical Sciences or equivalent |
| Job Function | Pharmacovigilance / Medical Writing |
| Work Arrangement | Hybrid / On-site / Remote, depending on location |
| Salary / CTC | Not specified |
| Job Type | Full-time |
| Application Mode | Online |
About Parexel
Parexel is a global clinical development and consulting organization serving the life sciences industry. The company works with biopharmaceutical organizations and research sites across areas such as clinical development, regulatory services, consulting and market access.
Its teams support clinical research and drug development programs with a focus on patient needs, scientific quality and regulatory requirements.
About the Medical Writer – Patient Safety Role
The Medical Writer I / Medical Writer II – Patient Safety position supports pharmacovigilance and drug-safety activities throughout the product lifecycle.
The role involves preparing regulatory safety documents, reviewing and analyzing safety information, conducting signal detection, performing literature searches and supporting risk management activities.
Medical Writer II professionals will additionally take on mentoring, complex client interactions, document review leadership and process improvement responsibilities.
Medical Writer I – Job Profile
Medical Writer I professionals will support the preparation of safety documents and pharmacovigilance deliverables while working with safety data from different sources.
The role requires the ability to analyze scientific information, prepare clear medical documents and work according to applicable regulatory and quality requirements.
Experience: 2+ years in pharmacovigilance, medical writing or a related field.
Medical Writer II – Job Profile
Medical Writer II is a more experienced position requiring 4+ years of relevant experience.
In addition to core medical writing and safety responsibilities, the role includes mentoring junior colleagues, handling complex client discussions, coordinating multi-stakeholder document reviews and contributing to process improvements.
Educational Qualification / Eligibility Criteria
Candidates should have a university degree in a relevant Life Sciences, Health Sciences or Biomedical Sciences discipline.
Relevant educational backgrounds may include:
- Pharmacy
- Microbiology
- Biochemistry
- Biotechnology
- Biophysics
- Dentistry
- Physiotherapy
- Other equivalent Life Sciences, Health or Biomedical Sciences qualifications
An equivalent combination of training and relevant work experience may also be considered.
Experience Requirements
The experience requirement depends on the position:
Medical Writer I
- 2+ years of experience in pharmacovigilance, medical writing or a related field.
Medical Writer II
- 4+ years of experience in pharmacovigilance, medical writing or a related field.
Candidates should also have an understanding of global pharmacovigilance regulations, medical terminology and safety-related concepts.
Required Skills and Qualifications
Applicants should have:
- Strong scientific and medical writing abilities.
- Analytical thinking and problem-solving skills.
- Understanding of pharmacovigilance principles.
- Knowledge of global drug-safety regulations.
- Familiarity with medical terminology and safety concepts.
- Experience working in regulated environments.
- Strong communication and interpersonal skills.
- Good organization and time-management abilities.
- Ability to prioritize multiple projects and deadlines.
- Strong attention to detail.
- Familiarity with medical writing tools and Microsoft Office applications.
- Knowledge of pharmacovigilance databases.
- Familiarity with coding dictionaries such as MedDRA and WHO-DD.
- Ability to collaborate with internal teams and external clients.
Key Responsibilities
The selected candidate may be responsible for the following activities:
Safety Report Preparation
- Prepare and coordinate scheduled and ad-hoc aggregate safety reports.
- Support development of PSURs, PBRERs, DSURs and other regulatory safety documents.
- Ensure safety documents are accurate and completed within required timelines.
- Support regulatory submissions across different regions.
Safety Signal Detection and Evaluation
- Perform independent signal detection using safety information from multiple sources.
- Analyze information from safety databases, clinical data, scientific literature and regulatory sources.
- Apply quantitative and qualitative approaches when evaluating potential safety signals.
- Prepare documents such as Drug Safety Reports (DSRs) and Signal Evaluation Reports (SERs).
- Integrate information from multiple sources to develop evidence-based safety assessments.
Literature Review
- Conduct systematic literature searches.
- Review published information relevant to product safety.
- Identify emerging safety trends.
- Support signal evaluation and epidemiological assessments through literature-based evidence.
Signal Tracking and Data Quality
- Maintain appropriate signal tracking records and logs.
- Identify discrepancies between safety data sources.
- Support resolution of data inconsistencies.
- Help maintain data integrity across safety deliverables.
Risk Management Activities
- Support the preparation and updating of Risk Management Plans (RMPs).
- Ensure safety information is appropriately reflected in related documentation.
- Work according to applicable regulatory requirements across therapeutic areas.
Client and Stakeholder Management
- Communicate with clients regarding routine project queries.
- Provide timely project status updates.
- Escalate complex issues when required.
- Adapt deliverables and communication according to client-specific requirements.
- Coordinate with multiple stakeholders during document preparation and review.
Compliance and Documentation
- Maintain documentation in an audit-ready condition.
- Ensure appropriate archiving of source materials.
- Support inspection-readiness activities.
- Follow applicable processes and regulatory requirements.
Additional Responsibilities for Medical Writer II
Medical Writer II professionals may also:
- Mentor junior team members.
- Provide technical and professional feedback.
- Lead complex client discussions.
- Coordinate multi-stakeholder document review cycles.
- Contribute to process improvement initiatives.
Preferred Qualifications
The following experience can be advantageous:
- Previous pharmacovigilance or safety assessment experience.
- Clinical exposure in hospital settings.
- Direct clinical research experience.
- Expertise in specific therapeutic areas or product categories.
- Familiarity with pharmacovigilance systems.
- Understanding of regulatory submission processes across multiple regions.
Work Location and Work Arrangement
Parexel has listed the position across the following locations:
- Hyderabad, India
- Bengaluru, India
- Mohali, India
- Mohali – Remote
- Hyderabad – Remote
The role is described as having hybrid, on-site or remote arrangements depending on the applicable location.
Candidates should verify the work arrangement associated with the specific position/location they select during the application process.
Salary / CTC
The salary or CTC for the Medical Writer I / Medical Writer II – Patient Safety position has not been disclosed in the provided job information.
Candidates should confirm compensation details with Parexel during the recruitment process.
Selection Process
The detailed recruitment and selection stages have not been specified in the available job description.
Candidates should follow the instructions provided through the official Parexel application process and be prepared for the company’s applicable assessment and interview stages.
How to Apply for Parexel Recruitment 2026
Interested and eligible candidates can apply online for the Medical Writer I / Medical Writer II – Patient Safety position.
Job Requisition ID: R0000046349
Before submitting the application, candidates should ensure that their resume clearly highlights relevant experience in pharmacovigilance, medical writing, safety reporting, signal detection, literature review and regulatory documentation.
Important Details Before Applying
- Parexel is recruiting for Medical Writer I / Medical Writer II – Patient Safety.
- The job requisition ID is R0000046349.
- Locations include Hyderabad, Bengaluru and Mohali.
- Remote options are listed for Hyderabad and Mohali.
- Medical Writer I requires 2+ years of relevant experience.
- Medical Writer II requires 4+ years of relevant experience.
- Relevant degrees include Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, Dentistry, Physiotherapy and other related disciplines.
- Knowledge of pharmacovigilance regulations and medical terminology is required.
- Experience with safety databases and coding dictionaries such as MedDRA and WHO-DD is relevant.
- Salary/CTC has not been disclosed.
- The position supports pharmacovigilance and patient-safety activities.
Frequently Asked Questions
1. What is the job title at Parexel?
The position is Medical Writer I / Medical Writer II – Patient Safety.
2. What is the Parexel job requisition ID?
The requisition ID is R0000046349.
3. Where are these Medical Writer jobs available?
The listed locations include Hyderabad, Bengaluru and Mohali, with remote options available for Hyderabad and Mohali.
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 qualifications are accepted?
Relevant university degrees in Life Sciences, Health or Biomedical Sciences are accepted, including Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, Dentistry and Physiotherapy.
7. What are the main responsibilities of the Medical Writer?
The role includes safety report preparation, signal detection and evaluation, literature review, signal tracking, risk management documentation, client coordination and regulatory compliance activities.
8. Is pharmacovigilance experience relevant to this position?
Yes. The role specifically supports patient-safety and pharmacovigilance activities, and prior pharmacovigilance experience is relevant to the position.
9. Which safety reports may the Medical Writer prepare?
The job description mentions PSURs, PBRERs, DSURs and other regulatory safety documents.
10. What coding dictionaries are relevant?
The position mentions familiarity with MedDRA and WHO-DD.
11. Is the Parexel Medical Writer job remote?
Remote positions are listed for Hyderabad and Mohali, while the overall role may also be hybrid or on-site depending on the selected location.
12. What is the salary for the Parexel Medical Writer position?
The salary/CTC has not been specified in the provided vacancy details.
Important Note
Job locations, work arrangements, eligibility criteria, compensation, recruitment stages and vacancy status may change according to Parexel’s hiring requirements. Candidates should verify the latest details on the official Parexel careers page before applying.