Clinical Research Associate Job at ICON | Healthcare Graduates Apply
A global clinical research associate job opportunity is now open at ICON plc in Mumbai. ICON is hiring CRA I/II professionals to support critical clinical monitoring activities within oncology and immunology studies. This healthcare job offers exposure to global clinical trials, structured career growth through ICON careers, and a strong professional pathway for candidates exploring Jobs in Mumbai within clinical research.
Job Details:
- Job Title: CRA I / II
- Location: Mumbai
- Job Reference: JR135624
- Division: Clinical Monitoring
- Department: ICON Strategic Solutions
- Position Type: Office-Based
About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization. The organization is recognized for fostering an inclusive environment that drives innovation and excellence while shaping the future of clinical development. ICON careers are built on scientific expertise, global collaboration, and high-quality clinical research, offering long-term healthcare job opportunities worldwide.
Job Description
ICON is currently seeking a Clinical Research Associate I / II to join its diverse and dynamic team in Mumbai. As part of this clinical research associate job, the role plays a pivotal part in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. This office-based position under ICON Strategic Solutions is well-suited for professionals seeking Jobs in Mumbai within global clinical research and long-term growth through ICON careers.
Qualifications
- Bachelor’s degree in a scientific or healthcare-related field.
- Minimum of 3 years of experience as a Clinical Research Associate & On-Site Monitoring
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Oncology/Immunology TA is mandatory.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Ability to travel at least 60% of the time (international and domestic – fly and drive) and should possess a valid driver’s license.
Key Responsibilities
- Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
