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Hiring Clinical, Regulatory, Drug Safety & Analytics Roles
🏢 Parexel
📍 India (Hybrid / Remote)
🎓 Life Sciences / MBBS
⏳ 0–8+ Years
Parexel is hiring for multiple high-demand roles in clinical research, pharmacovigilance, regulatory affairs, and analytics. These roles offer strong career growth in CRO and pharma industry.
👉 Not sure which career to choose? Read: Healthcare IT vs Clinical Career Guide
🧪 Clinical Operations Associate (0–1 Years)
- Maintain Trial Master File (TMF) and essential documents
- Update CTMS and track study progress
- Support site activation, monitoring, and close-out
- Coordinate with CRAs, sponsors, and investigators
- Ensure compliance with ICH-GCP guidelines
Tools Used: CTMS, eTMF, Excel
Career Growth: CTA → CRA → Clinical Project Manager
👉 Learn basics: Clinical Research Career Guide
📊 Regulatory Affairs Associate (5–8 Years)
- Prepare global submissions (US FDA, EMA)
- Handle CMC documentation and lifecycle management
- Ensure compliance with regulatory guidelines
- Work on dossier publishing and submission tools
Skills: eCTD, Regulatory Writing, Global Guidelines
Career Growth: RA Associate → RA Manager → Global Head
📄 Medical Device Documentation (3–6 Years)
- Prepare technical documentation for medical devices
- Work on CE marking and regulatory approvals
- Ensure compliance with ISO and global device standards
Industry Demand: High growth in medical devices & diagnostics
💊 Drug Safety Physician (5–10+ Years)
- Medical review of ICSR cases
- Signal detection and risk management
- Ensure pharmacovigilance compliance
- Work on benefit-risk assessment
Qualification: MBBS / MD
👉 Practice PV concepts: Pharmacovigilance Quiz
📈 Visual Analytics Specialist (1–3 Years)
- Build dashboards using R / R Shiny
- Analyze clinical trial datasets
- Create reports and insights
- Support decision-making with data
Skills: R, SQL, Data Visualization
👉 Learn analytics: Clinical Data vs SAS Guide
💡 Interview Preparation Tips
- Revise ICH-GCP guidelines
- Understand clinical trial lifecycle
- Prepare domain-specific questions
- Top 100 Questions
- Aptitude Practice
📄 Resume Optimization Tips
- Use ATS keywords: GCP, TMF, ICSR, CTMS
- Highlight projects & internships
- Show measurable achievements
- Resume Guide
🚀 Job Application Links (Parexel)
🚀 Apply Now: Clinical Operations Associate
🚀 Apply Now: Senior Regulatory Affairs Associate
🚀 Apply Now: Senior Medical Device Documentation Associate
🚀 Apply Now: Senior Drug Safety Physician
🚀 Apply Now: Real-time Visual Analytics Specialist
📌 Important Note Before You Apply:
Kindly read the full job description carefully for your selected role before applying. Ensure your profile, qualifications, and core competencies align with clinical monitoring operations, healthcare regulatory affairs dossiers, medical device compliance documentation, pharmacovigilance medical review, or real-time visual analytics dashboard configuration workflows before proceeding.
Kindly read the full job description carefully for your selected role before applying. Ensure your profile, qualifications, and core competencies align with clinical monitoring operations, healthcare regulatory affairs dossiers, medical device compliance documentation, pharmacovigilance medical review, or real-time visual analytics dashboard configuration workflows before proceeding.
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