Senior Medical Writer Role at Parexel | PV or Regulatory Writing
- About Parexel
- Current Openings
- Accepted Educational Background & Courses
- Key Responsibilities
- Required Skills & Competencies
- 📩 How to Apply
- Company & Job Summary Table
Senior Medical Writer Role at Parexel | Remote India | Life Sciences/Pharmacy Graduates with Experience in PV or Regulatory Writing
Apply now for Senior Medical Writer positions at Parexel (Remote, India). Open to Pharmacy, Life Sciences, Medical, or Allied Health graduates with relevant experience in pharmacovigilance or regulatory writing.
Join Parexel as a Senior Medical Writer – Work from Home, India
Are you a skilled scientific communicator with a passion for regulatory and safety documentation? Parexel, a global CRO, is looking for a Senior Medical Writer to join their Medical Writing team on a full-time remote basis from anywhere in India. This opportunity is ideal for experienced professionals in pharmacovigilance, signal detection, or regulatory writing who want to work on global clinical research projects.
About Parexel
Parexel is one of the world’s leading Contract Research Organizations (CROs), working with biopharma companies to bring life-changing therapies to market. Their culture fosters inclusion, innovation, and ongoing development, offering opportunities to grow your scientific career remotely.
Current Openings
Position: Senior Medical Writer
- Location: Remote (India)
- Experience Required: Minimum 2+ years in Pharmacovigilance/Medical Writing
- Required Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biochemistry, Biotechnology, Nursing, or related medical field
- Department: Medical Writing – Pharmacovigilance & Regulatory Affairs
Accepted Educational Background & Courses
Degrees:
- B Pharm / M.Pharm
- BSc. / MSc. in Biotechnology, Biochemistry, Microbiology, Biophysics
- MBBS / BDS / BPT / BAMS / BHMS
- Nursing (GNM, BSc. Nursing)
Relevant Training:
- Signal Detection & Risk Management
- Pharmacovigilance Reporting Guidelines
- Clinical Document Review & ICH-GCP Standards
- Scientific & Medical Writing Certification
Key Responsibilities
- Author pharmacovigilance documents, signal management reports, and HA responses
- Manage end-to-end signal evaluation process – assessment, meetings, presentations
- Collaborate with cross-functional teams to ensure compliance and data accuracy
- Perform literature reviews and data extraction from safety databases and journals
- Assist with regulatory submissions, benefit-risk assessments, and product safety documents
- Mentor junior team members and deliver training sessions when needed
Required Skills & Competencies
- Strong command of scientific writing and safety documentation
- Familiarity with global regulatory and ICH-GCP guidelines
- Experience in CTMS/eTMF systems and document tracking
Analytical mindset with attention to medical detail
Excellent communication and client-facing skills
Ability to manage timelines, deliverables, and complex medical texts
📩 How to Apply
Apply directly via the Parexel career portal:
👉 Apply Here
🗓️ Last date to apply: Not specified (Apply as early as possible)
Tag someone who may benefit from this work-from-home opportunity in medical writing!
Company & Job Summary Table
| Company Name | Current Vacancies in Departments | Required Education | Experience Required |
|---|---|---|---|
| Parexel | Medical Writing (PV/Regulatory) | B Pharm, M.Pharm, Life Sciences, Nursing, MBBS, BDS, etc. | 2+ years in PV or Regulatory Writing |
Start or elevate your remote career in scientific writing with Parexel – where science meets communication.
To apply for this job please visit jobs.parexel.com.
