Job Title: Clinical Research Associate II
Location: Delhi, India (Office or Home – Strategic Solutions Program)
Employment Type: Full-Time
Job ID: JR137236
Company Overview:
ICON plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment that drives innovation and excellence. ICON supports clinical development and innovative treatments through high-quality data and trial management.
Role Summary:
As a Clinical Research Associate II, you will oversee clinical trial activities, ensuring protocol compliance, data integrity, and patient safety. You will collaborate with site staff, review data, and contribute to study documentation for clinical trials.
Key Responsibilities:
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborate with investigators and site staff to facilitate smooth study conduct.
Perform data review and resolve queries to maintain high-quality clinical data.
Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
Qualifications & Profile:
Bachelor’s degree in a scientific or healthcare-related field.
Minimum 3 years of on-site monitoring experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills with attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.
Willingness to travel as required (train, car, bus, air).
Benefits & Opportunities:
Competitive salary and annual leave entitlements.
Health insurance options for you and your family.
Retirement planning offerings.
Global Employee Assistance Program (LifeWorks) providing 24-hour support.
Life assurance.
Flexible country-specific optional benefits (e.g., childcare vouchers, bike schemes, gym memberships, subsidized travel, health assessments).
Inclusion & Diversity:
ICON is committed to an inclusive and accessible environment, providing equal employment opportunities for all applicants regardless of race, color, religion, sex, sexual orientation, gender identity, disability, veteran status, or other protected categories.
Reasonable accommodations available for applicants with medical conditions or disabilities.
Additional Notes:
Candidates are encouraged to apply even if they do not meet all requirements.
Opportunity to gain hands-on experience in clinical monitoring, trial management, and data integrity.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | Tarasadi | Vadodara | Vapi |Maharashtra :
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Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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Rangpo |India :
Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Japan | Saitama |Tokyo :
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