ICON Clinical Site Associate Jobs India
- ICON Hiring Clinical Site Associate | Freshers & Entry-Level Clinical Research Jobs in Bangalore, Chennai & Trivandrum
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Summary Table
ICON Hiring Clinical Site Associate | Freshers & Entry-Level Clinical Research Jobs in Bangalore, Chennai & Trivandrum
ICON plc is hiring for Clinical Site Associate roles under its Clinical Monitoring and Clinical Operations division. This is a hybrid, full-time opportunity open across Bangalore, Chennai, and Trivandrum. The role is ideal for freshers and candidates with initial experience in clinical research, making it a strong entry-level opportunity in the CRO industry. While the exact number of vacancies is not disclosed, multiple openings are expected across project teams supporting global clinical trials.
This position offers direct exposure to site management, clinical trial coordination, regulatory documentation, and real-world drug development processes.
Company Overview
ICON plc is a globally recognized clinical research organization (CRO) providing healthcare intelligence and clinical development services to pharmaceutical, biotechnology, and medical device companies. The company supports clinical trials across all phases, helping bring innovative therapies to market faster.
With a strong presence in over 100 countries, ICON is known for its scientific expertise, regulatory excellence, and data-driven clinical solutions. The organization focuses on improving patient outcomes through efficient clinical trials, advanced analytics, and global collaboration.
Working at ICON provides professionals with access to international clinical projects, structured training, and career progression in clinical research, pharmacovigilance, and regulatory affairs.
Job Role & Responsibilities
As a Clinical Site Associate, you will support site management activities and ensure smooth execution of clinical trials.
- Assist in site activation by collecting, reviewing, and tracking regulatory documents
- Maintain accurate site data in clinical trial systems such as CTMS and eTMF
- Support Clinical Research Associates (CRAs) in site communication and follow-ups
- Coordinate logistics for site visits, meetings, and documentation
- Ensure proper filing of essential documents for audit and inspection readiness
- Track site progress and resolve documentation or operational issues
- Support site payments and administrative processes
- Contribute to process improvements and operational efficiency initiatives
This role is crucial in ensuring clinical trials are conducted efficiently, compliantly, and in line with global regulatory standards.
Eligibility / Qualifications
Candidates must meet the following criteria:
- Bachelor’s degree in Life Sciences, Pharmacy, Healthcare, Business, or related field
- Freshers or candidates with initial experience in clinical research or administration can apply
Relevant courses include: B.Pharmacy, M.Pharmacy, BSc Life Sciences, MSc Clinical Research, MSc Biotechnology, Pharm.D, BBA Healthcare Management
Key skills required:
- Strong organizational and multitasking abilities
- Attention to detail and documentation accuracy
- Basic knowledge of clinical trials and regulatory guidelines (preferred)
- Good communication and interpersonal skills
- Proficiency in MS Office and clinical systems
- Ability to work in a team and adapt to dynamic project environments
Location & Salary
- Locations: Bangalore, Chennai, Trivandrum (Hybrid Work Model)
- Salary: Approximately ₹4 LPA – ₹8 LPA (based on entry-level clinical research roles in India)
Application Process
Interested candidates can apply through the official ICON careers portal:
Apply Here: https://careers.iconplc.com/job/clinical-site-associate-in-india-chennai-jid-50147
Ensure your resume highlights your academic background, internship experience, and knowledge of clinical research processes to improve your chances of selection.
Frequently Asked Questions (FAQs)
1. Is this job suitable for freshers?
Yes, freshers and candidates with minimal experience can apply.
2. What is the role of a Clinical Site Associate?
The role involves supporting clinical trial site activities, documentation, and coordination.
3. What qualifications are required?
A bachelor’s degree in Life Sciences, Pharmacy, or related fields is required.
4. Is this a remote job?
No, this is a hybrid role with office-based work.
5. What career growth can I expect?
You can progress to roles such as Clinical Research Associate (CRA), Study Coordinator, or Clinical Project Manager.
Summary Table
| Company | ICON plc |
|---|---|
| Vacancies | Clinical Site Associate |
| Required Education | B.Pharmacy, M.Pharmacy, BSc Life Sciences, MSc Clinical Research, Pharm.D, BBA |
| Experience | Freshers / Entry-Level |
To apply for this job please visit careers.iconplc.com.