Site Services Specialist I at ICON Bangalore | Clinical Trials – Apply Now
An ICON clinical research Bangalore opportunity is available for aspiring clinical research professionals. The organization is seeking a Site Services Specialist I to support clinical trial sites, ensuring they are equipped with the necessary resources to conduct trials effectively. This entry-level position suits candidates with a background in life sciences or healthcare administration.
About ICON clinical research Bangalore
Moreover, ICON plc is a global healthcare intelligence and clinical research organization dedicated to bringing new medicines and treatments to patients faster. With a strong commitment to integrity, collaboration, agility, and inclusion, ICON operates in various locations, including Bengaluru, Karnataka, India, where they focus on clinical trials and site management.
- Company: ICON plc (ICON India Clinical)
- Location: Bengaluru, Karnataka, India (office with flex)
- Experience: No mandatory years. Relevant clinical research / site management / clinical operations experience preferred.
- Qualification: Bachelor’s in life sciences, healthcare administration, clinical research, or related field.
- Posted: 28 August 2026
- Deadline: Not specified
ICON clinical research Bangalore job description
As a Site Services Specialist I at ICON, the individual will contribute to clinical research activities by managing logistics, resolving site-related issues, and ensuring that clinical trial sites are well-equipped. Additionally, the role involves working collaboratively with cross-functional teams and supporting the overall study objectives.
Key Responsibilities
- First, providing logistical and operational support to clinical trial sites for this ICON clinical research Bangalore role, ensuring timely and efficient delivery of materials and supplies.
- Additionally, assisting in resolving site-related issues, troubleshooting operational challenges, and ensuring adherence to study protocols.
- Moreover, collaborating with cross-functional teams to ensure seamless communication between trial sites and ICON teams.
- Tracking site performance metrics and providing reports to support study timelines and goals.
- Finally, ensuring compliance with Good Clinical Practice (GCP) and applicable regulatory requirements across all site activities.
Eligibility Criteria
- Bachelor’s degree in a relevant field such as life sciences, healthcare administration, or clinical research.
- Experience in site management, clinical operations, or a related field is preferred.
- Strong problem-solving and organizational skills, with the ability to manage multiple tasks and deadlines.
- Knowledge of clinical trial processes, GCP, and regulatory requirements is a plus.
- Excellent communication and interpersonal skills, with the ability to work effectively within a cross-functional team.
- Willingness to travel as required (approximately 1%).
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support health, wellbeing, and career development. Benefits may include:
- Competitive base salary and performance-related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.
Benefits may vary depending on role and location. Visit the ICON careers site to read more about the benefits offered.
Inclusion and Accessibility
ICON is an equal opportunity employer committed to building an inclusive and accessible workplace where everyone feels valued and supported. If reasonable accommodations are required during the recruitment process, candidates are encouraged to submit a request.
This ICON clinical research Bangalore position represents an excellent opportunity for candidates looking to start their career in clinical research. Therefore, interested individuals should apply at the earliest to be considered for this role.
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