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Hiring Project Analyst, CDM & Regulatory Roles
🏢 ICON plc
📍 Bangalore / Trivandrum / Chennai
💊 Clinical Research
📊 Clinical Data Management
📑 Regulatory Affairs
ICON plc is actively hiring for multiple Clinical Research, Clinical Data Management, and Regulatory Affairs roles across India.
The company has announced openings for:
- Project Analyst I
- Clinical Data Coordinator (Immediate Joiners)
- Senior Global Regulatory Scientist
These opportunities are ideal for freshers, early-career professionals, and experienced regulatory professionals looking to grow in the CRO and pharmaceutical industry.
📘 Career Guide: Clinical SAS vs Clinical Data Guide
📋 ICON Recruitment 2026 – Overview
- Company: ICON plc
- Industry: Clinical Research / CRO / Regulatory Affairs
- Employment Type: Full-Time
- Mode: Office or Home / Hybrid
- Experience: 0–3+ Years
- Locations: Bangalore, Trivandrum, Chennai
📊 1. Project Analyst I
- Location: Bangalore
- Experience: Freshers & Early Career Professionals
- Qualification: Life Sciences / Pharmacy / Healthcare / Biotechnology
- Work Mode: Office or Home
- Estimated Salary: ₹4 – ₹7 LPA
📌 Key Responsibilities
- Support project execution activities
- Track KPIs and operational metrics
- Assist in risk management processes
- Coordinate project suppliers and resources
- Participate in project meetings and issue resolution
- Support process improvement initiatives
💻 Required Skills
- Analytical & organizational skills
- Stakeholder management
- Problem-solving mindset
- Attention to detail
- Project coordination understanding
- Communication skills
📚 Learn Project Coordination Basics: Healthcare IT vs Clinical Healthcare
📑 2. Clinical Data Coordinator (CDC I)
- Location: Bangalore & Trivandrum
- Experience: Freshers & Experienced
- Qualification: Life Sciences / Pharmacy / Biotechnology / Healthcare
- Work Mode: Office or Home
- Estimated Salary: ₹3.8 – ₹6.5 LPA
📌 Key Responsibilities
- Support eCRF development activities
- Assist in query generation and resolution
- Review clinical and third-party study data
- Support study documentation and archiving
- Coordinate with data scientists and project teams
- Maintain data quality and compliance
💻 Required Skills
- Clinical Data Management basics
- Knowledge of Medidata or Oracle RDC preferred
- Understanding of ICH-GCP guidelines
- Communication and documentation skills
- Attention to detail
📊 Learn Clinical Data Basics: Clinical SAS PDV Guide
📑 3. Senior Global Regulatory Scientist
- Locations: Bangalore / Trivandrum / Chennai / Kuala Lumpur / Seoul
- Experience: Minimum 3 Years
- Qualification: Scientific or Related Discipline
- Work Mode: Hybrid
- Estimated Salary: ₹12 – ₹22 LPA
📌 Key Responsibilities
- Coordinate regulatory submissions and ethics committee activities
- Develop global clinical trial submission strategies
- Manage regulatory documentation and compliance
- Support budget management and regulatory consulting
- Maintain regulatory intelligence and CTMS updates
- Lead stakeholder communication activities
💻 Required Skills
- Global regulatory guidelines knowledge
- Clinical trial submission experience
- Leadership & communication skills
- Regulatory affairs expertise
- Project management abilities
- CTMS and documentation handling
📚 Learn Regulatory Documentation: Clinical Documentation & CDISC Guide
🎁 Benefits Offered by ICON
- Competitive salary packages
- Hybrid work flexibility
- Health insurance coverage
- Retirement and savings benefits
- Employee Assistance Programme
- Paid leave and wellness benefits
- Career growth and learning opportunities
- Global CRO exposure
🎓 Eligible Qualifications
- B.Pharm
- M.Pharm
- Pharm.D
- BSc / MSc
- Life Sciences
- Healthcare
- Biotechnology
- Related Scientific Discipline
❓ Frequently Asked Questions
- Are freshers eligible? Yes, freshers can apply for Project Analyst I and CDC I roles.
- Which roles require experience? Senior Global Regulatory Scientist requires 3+ years experience.
- What work mode is offered? Office, Home, and Hybrid modes depending on role.
- What systems are preferred? Medidata, Oracle RDC, CTMS, and eTMF exposure.
- Which locations are available? Bangalore, Trivandrum, Chennai, Kuala Lumpur, and Seoul.
🧠 Prepare Before Applying
💡 Interview Tips
- Revise Clinical Research and CRO basics
- Understand ICH-GCP guidelines and clinical trial workflow
- Practice communication and stakeholder management questions
- Prepare examples for teamwork and problem-solving situations
- For CDM roles, revise query management and eCRF concepts
- For Regulatory roles, revise submission and compliance concepts
- Be confident while explaining your projects and internships
📊 Practice Interview Questions: Clinical & Data Interview Preparation Guide
📄 Resume Tips
- Keep your resume clean and ATS-friendly
- Highlight Clinical Research, Pharmacovigilance, or CDM skills clearly
- Add internships, projects, certifications, and workshops
- Mention software/tools like Medidata, Oracle RDC, CTMS, or Excel if known
- Include communication and analytical skills
- Keep resume length within 1–2 pages
- Use proper formatting and avoid spelling mistakes
📚 Career Guidance: Healthcare Career Knowledge Hub
🚀 Apply Now
📌 Note Before You Apply:
Kindly read the complete job description carefully before applying. Ensure your qualifications, skills, and experience align with the selected role requirements before proceeding.
Kindly read the complete job description carefully before applying. Ensure your qualifications, skills, and experience align with the selected role requirements before proceeding.
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