Site Services Specialist I – ICON plc | Clinical Data Management & Life Science Jobs
Join ICON plc, a global leader in clinical research and healthcare intelligence, as a Site Services Specialist I. This role offers the chance to contribute to groundbreaking clinical data management operations supporting clinical trial sites across India. If you’re looking to advance your career in life science jobs with a company that drives innovation and excellence, this opportunity is for you.
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to transforming clinical development. With a global team dedicated to innovation, ICON supports pharmaceutical, biotechnology, and medical device companies in accelerating the development of life-saving treatments. Known for its inclusive, diverse, and high-performing work culture, ICON plc careers empower professionals to grow while making a lasting impact on global health.
Job Overview:
As a Site Services Specialist I, you will play a key role in coordinating clinical site operations, managing logistics, and ensuring the efficient execution of clinical trials. Based in Bangalore (Hybrid, Office-Based), this position supports clinical data management and site activities critical to the success of ICON’s global studies.
- Location: Bangalore, India (Hybrid)
- Position: Full-time
Qualifications:
- Bachelor’s degree in Life Sciences, or Clinical Research
- Prior experience in site management, clinical operations, or clinical data management preferred
- Understanding of GCP guidelines and regulatory compliance
- Excellent organizational and communication skills
- Strong problem-solving abilities and attention to detail
Key Responsibilities:
- Provide operational and logistical support to clinical trial sites.
- Manage timely delivery of study materials and ensure site readiness.
- Resolve site-related issues and ensure protocol adherence.
- Collaborate with cross-functional teams to streamline communication.
- Track and report site performance metrics to support project timelines.
- Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements.
Skills Required:
- Strong understanding of clinical data management and trial site coordination
- Proficiency in MS Office and related systems
- Excellent interpersonal and communication skills
- Ability to multitask and meet deadlines
- Detail-oriented, proactive, and adaptable team player
Join ICON plc and become part of a team transforming global clinical development through cutting-edge clinical data management and operational excellence. If you’re passionate about meaningful life science jobs that make a difference in healthcare, this is your opportunity to grow with a world leader.
How to Apply:
Interested candidates can apply through the official ICON careers portal for more details and current openings.
