Clinical Research Associate I
ICON Strategic Solutions
Vijayipur, Bihar, India0–2 yrs5d agovia LinkedIn
About the Role
As a Clinical Research Associate I at ICON, you will contribute to clinical trial operations, delivering high-quality outcomes across clinical programs. This role involves sponsor-dedicated work, supported by ICON’s global expertise.
Key Responsibilities
- Coordinate all activities for setting up and monitoring a study, working independently and actively.
- Complete accurate study status reports and maintain study documentation.
- Run sponsor-generated queries efficiently.
- Take responsibility for study cost efficiency.
- Participate in the preparation and review of study documentation.
- Participate in feasibility studies for new proposals as required.
- Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
- Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.
Requirements & Tech Stack
- Clinical trial monitoring experience
- ICH-GCP guidelines knowledge
- Expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills to deal with queries in a timely manner
- Willingness to travel (approximately 60%)
Qualifications
- University degree in medicine, science, or equivalent