For Medical Writer I, the focus is on developing, editing, and reviewing clinical documentation, supporting literature research, analyzing study information, and working with cross-functional teams.
Job Overview
| Particulars | Details |
|---|---|
| Position | Medical Writer |
| Company | Parexel |
| Location | Bengaluru |
| Job Type | Remote |
| Category / Department | Scientific Writer |
| Application Mode | Online |
🏢 About Parexel
Parexel is a global clinical development partner supporting organizations across the Life Sciences industry.
The company works with biopharmaceutical companies, emerging innovators, research sites, and other stakeholders to help plan and deliver clinical development programs.
Its services span areas including clinical research, regulatory support, consulting, and therapeutic expertise, with a focus on helping move promising treatments through development and toward patients.
With a global workforce and decades of experience in clinical development, Parexel brings together scientific knowledge, local understanding, and international capabilities to support complex research programs.
The company's approach emphasizes collaboration, patient-focused clinical research, innovation, and reliable execution across the development journey.
🎯 COMPANY MISSION
Parexel's work is centered on helping the Life Sciences industry advance clinical research and bring meaningful healthcare innovations closer to patients.
Its patient-focused approach aims to make clinical research more accessible while supporting biopharmaceutical organizations throughout the clinical development process.
💡 Editor's Note / Preparation Tip
📌 The recruitment information provided lists two positions: Medical Writer I and Senior Medical Writer.
📌 The roles are listed as remote opportunities based in India, with Bengaluru mentioned as the location.
📌 Experience expectations may differ between the two positions.
📌 Medical Writer I candidates may be considered with early-career experience, while Senior Medical Writer applicants should have stronger professional medical-writing experience.
📌 Candidates should tailor their resume according to the specific position they are applying for.
📌 Relevant experience in CROs, pharmaceutical companies, biotechnology organizations, or medical communications can strengthen an application.
📌 Knowledge of clinical documents, regulatory requirements, and ICH-GCP can be valuable.
📌 The stated application deadline is 30 August 2026; candidates should verify the latest vacancy status and deadline on the official Parexel careers portal before applying.
📄 RESUME PREPARATION TIPS
1️⃣ Highlight your medical, scientific, or regulatory writing experience prominently on your resume.
2️⃣ List specific documents you have worked on, such as CSRs, Protocols, Investigator Brochures, Patient Narratives, Clinical Summaries, or CTD documents.
3️⃣ Mention your exposure to clinical trials, ICH-GCP, regulatory requirements, literature review, and clinical data interpretation.
4️⃣ Showcase collaboration with teams such as Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, and Medical Affairs.
5️⃣ For Senior Medical Writer applications, highlight document ownership, project leadership, review management, mentoring, and stakeholder coordination.
🎯 INTERVIEW PREPARATION
1️⃣ Review the purpose and structure of common clinical documents, particularly CSRs, Protocols, Investigator Brochures, and CTD documents.
2️⃣ Be prepared to explain how you approach researching, drafting, reviewing, and finalizing a scientific document.
3️⃣ Refresh your understanding of ICH-GCP and major regulatory expectations, including the role of FDA and EMA requirements.
4️⃣ Prepare examples of how you handled reviewer comments, conflicting feedback, tight deadlines, or multiple document revisions.
5️⃣ Practice explaining complex clinical or scientific information in a clear and concise manner.
💡 PROFESSIONAL TIPS
🚀 Build expertise in both scientific writing and clinical research fundamentals.
📚 Keep improving your knowledge of clinical and regulatory documentation.
✍️ Maintain a small portfolio of writing samples where confidentiality permits.
🤝 Develop strong stakeholder-management skills because medical writing is highly collaborative.
🧠 Learn to interpret scientific and statistical information without losing accuracy or context.
📝 Job Description
PAREXEL IS HIRING | MEDICAL WRITER I & SENIOR MEDICAL WRITER 🧬📝
🏠 Remote | Bengaluru, India | Full-Time | 0–5 Years | Medical & Regulatory Writing
Are you from a Pharmacy, Life Sciences, Medicine, Biotechnology, or Healthcare background and interested in building a career in medical writing?
Parexel is hiring for Medical Writer I and Senior Medical Writer opportunities in India. These remote roles offer professionals the chance to work on clinical and regulatory documents that support global drug development programs and contribute to the advancement of new therapies.
If you enjoy scientific writing, literature review, clinical research, and working with complex medical information, this could be an exciting opportunity to develop your career while collaborating with global pharmaceutical and biotechnology teams. 🚀
📌 JOB DETAILS
🏢 Company: Parexel
💼 Positions: Medical Writer I / Senior Medical Writer
📍 Location: Bengaluru, India
🏠 Work Mode: Remote
⏰ Employment Type: Full-Time
🧬 Department: Medical Writing
🏥 Industry: CRO / Clinical Research
🎓 Qualification: B.Pharm, M.Pharm, B.Sc./M.Sc. Life Sciences, Biotechnology, Pharmacy, Medicine, MBBS, PharmD, MD, PhD, or another relevant Healthcare/Life Sciences degree
💼 Experience: 0–5 Years
📅 Posted: 31 July 2026
📅 Stated Application Deadline: 30 August 2026
🌟 PREFERRED SKILLS & EXPERIENCE
🔹 Experience in medical, scientific, or regulatory writing
🔹 Previous exposure to CRO, pharmaceutical, biotechnology, healthcare, or medical communications environments
🔹 Experience preparing clinical and regulatory documents
🔹 Knowledge of clinical development processes
🔹 Experience with CSRs, Protocols, Investigator Brochures, Clinical Summaries, Clinical Overviews, or CTD documents
🔹 Familiarity with global clinical research and regulatory requirements
🔹 Strong project coordination and stakeholder-management abilities
🎓 EDUCATION & EXPERIENCE
Candidates from the following academic backgrounds may be considered:
🎓 B.Pharm
🎓 M.Pharm
🎓 B.Sc. Life Sciences
🎓 M.Sc. Life Sciences
🎓 Biotechnology
🎓 Pharmacy
🎓 Medicine
🎓 MBBS
🎓 PharmD
🎓 MD
🎓 PhD
🎓 Other relevant Healthcare or Life Sciences qualifications
Medical Writer I: Candidates with 0–5 years of experience may be relevant, with medical or scientific writing experience preferred.
🎯 Key Responsibilities
- ✓ Write, edit, and review clinical and regulatory documents.
- ✓ Support preparation of Clinical Study Reports (CSRs).
- ✓ Contribute to Interim Study Reports and Patient Narratives.
- ✓ Assist with Safety Update Reports and Informed Consent Forms (ICFs).
- ✓ Conduct literature searches and scientific reviews.
- ✓ Review clinical study information and prepare scientific documentation.
- ✓ Follow relevant ICH-GCP requirements and applicable regulatory standards.
- ✓ Perform document quality checks for accuracy, consistency, and completeness.
- ✓ Participate in document review cycles and manage stakeholder feedback.
- ✓ Collaborate with Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, and Medical Affairs teams.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Medical Writer role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
1️⃣ Who can apply for the Medical Writer I position?
Professionals with relevant qualifications in Pharmacy, Life Sciences, Biotechnology, Medicine, or related healthcare disciplines may be considered. Early-career candidates with relevant scientific or medical writing exposure may be suitable.
2️⃣ What is the experience requirement for Senior Medical Writer?
The Senior Medical Writer position is intended for candidates with stronger prior experience in medical writing, particularly within CRO, pharmaceutical, biotechnology, or related organizations.
3️⃣ Is this a remote opportunity?
Yes. The provided job information lists the opportunities as Remote, with Bengaluru, India, mentioned as the location.
4️⃣ What documents might a Medical Writer work on?
Depending on the position and project, responsibilities may include Clinical Study Reports, Protocols, Investigator Brochures, Patient Narratives, Clinical Summaries, Clinical Overviews, Safety Reports, and CTD documentation.
5️⃣ Can Pharmacy and Life Sciences graduates build a career in Medical Writing?
Yes. Pharmacy, Life Sciences, Biotechnology, Medicine, and related educational backgrounds can provide a strong scientific foundation for medical writing. Strong communication and writing skills are equally important.
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