Clinical Trial Associate Job in Bengaluru at ICON plc for professionals with CTMS, NDCT rules, and regulatory submission experience.
About the Company
ICON plc is a globally recognized Clinical Research Organization (CRO) providing comprehensive clinical development and drug commercialization services to the pharmaceutical, biotechnology, and medical device industries. ICON supports clinical trials across all phases and therapeutic areas, helping bring innovative and life-changing treatments to patients worldwide.
With a strong global presence and a reputation for quality, compliance, and scientific excellence, ICON plc offers professionals the opportunity to work on complex international studies in a collaborative and growth-oriented environment.
Job Details
- Job Title: Clinical Trial Associate
- Company: ICON plc
- Location: Bengaluru, Karnataka, India
- Experience Required: 2 – 4 Years
- Qualification: B.Pharm, M.Pharm, Pharm.D, BSc, MSc (Life Sciences)
- Employment Type: Full-Time, Permanent
- Industry: Pharmaceutical & Life Sciences
- Number of Openings: 1
- Joining Timeline: Immediate or within 30 days
- Job Status: Verified Job
- Application Mode: Online
Job Description
ICON plc is hiring a Clinical Trial Associate to support end-to-end clinical trial operations at its Bengaluru location. This role is ideal for professionals with hands-on experience in clinical trial coordination, regulatory documentation, and Clinical Trial Management Systems (CTMS). Clinical Trial Associate Job in Bengaluru
The Clinical Trial Associate will work closely with cross-functional teams to ensure clinical trials are conducted in compliance with study protocols, ICH-GCP guidelines, NDCT rules, and applicable regulatory requirements. Clinical Trial Associate Job in Bengaluru
Key Responsibilities
- Assist in the coordination and administration of clinical trials in accordance with protocols and regulatory standards
- Maintain, organize, and track essential clinical trial documentation and study files
- Support regulatory submissions to Ethics Committees (EC) and Institutional Review Boards (IRB)
- Assist in preparation and review of study documents such as Informed Consent Forms (ICF) and Case Report Forms (CRF)
- Update and maintain clinical trial data in CTMS and related systems
- Track clinical trial milestones, metrics, and deliverables
- Coordinate with internal teams to ensure smooth execution of trial activities
- Support compliance with ICH-GCP, NDCT rules, and company SOPs
Clinical Trial Associate Job in Bengaluru
Skills / Qualifications
Educational Qualifications
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related healthcare discipline
Experience Requirements
- 2 to 4 years of relevant experience in clinical research or clinical trial operations
- Hands-on experience with:
- Clinical Trial Management Systems (CTMS)
- NDCT Rules and Indian regulatory requirements
- EC and IRB submissions
Technical & Professional Skills
- Strong understanding of clinical trial processes and regulatory guidelines
- Knowledge of ICH-GCP and applicable local regulations
- Excellent documentation, organizational, and communication skills
- Ability to work effectively in a fast-paced CRO environment
- Strong attention to detail and compliance-driven mindset
Clinical Trial Associate Job in Bengaluru
Salary & Benefits
- Estimated Salary Range: ₹5,00,000 – ₹9,00,000 per annum (as per Bengaluru industry standards)
- Opportunity to work on global clinical trials
- Exposure to international sponsors and stakeholders
- Professional training and compliance-focused work culture
- Clear career growth opportunities within a leading global CRO
Clinical Trial Associate Job in Bengaluru
Why You Should Join
Joining ICON plc as a Clinical Trial Associate provides an opportunity to work in a globally respected CRO environment focused on innovation, quality, and patient safety. Employees gain exposure to diverse therapeutic areas, structured learning, and long-term career progression within clinical research. Clinical Trial Associate Job in Bengaluru
ICON values collaboration, scientific integrity, and professional development, making it an ideal workplace for clinical research professionals looking to advance their careers.
How to Apply
Early applications are encouraged due to limited openings.
FAQs
Is this role suitable for candidates with CRO experience only?
CRO experience is preferred, but candidates with relevant clinical research exposure may also apply.
Is this a full-time position?
Yes, this is a full-time, permanent role.
Is CTMS experience mandatory?
Yes, hands-on experience with CTMS is required.
What is the work location?
The position is based in Bengaluru, Karnataka.
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