What are the responsibilities and job description for the Clinical Research Associate (CRA) II / Senior CRA position at i-Pharm Consulting?
Job Title : Clinical Research Associate (CRA) II / Senior CRA
Job Type : Permanent Full Time
Location : United States - All States
Must Have : Minimum 2 Years of On Site Monitoring Experience & 1 Year of Oncology Experience
Our client is a global leader in healthcare data, technology, and advanced analytics, dedicated to supporting the pharmaceutical and biotechnology industries in the development of ground-breaking treatments. With a strong focus on oncology, our mission is to accelerate the discovery and development of life-changing therapies. They are seeking a highly skilled Clinical Research Associate II (CRA II) to join our team and contribute to the success of cutting-edge oncology clinical trials.
Key Responsibilities :
- Oversee and manage the progress of clinical trials at investigational sites, ensuring adherence to the study protocol, ICH-GCP, and local regulatory requirements.
- Conduct site initiation, monitoring, and close-out visits, offering continuous support to ensure optimal site performance.
- Establish and maintain strong working relationships with investigators, site staff, and other key stakeholders.
- Ensure accurate and timely collection and reporting of clinical trial data.
- Proactively identify potential risks and work with the study team to resolve issues affecting timelines, data quality, or compliance.
- Provide guidance to junior CRAs and assist in their professional development.
- Ensure all clinical trial documentation is maintained in compliance with regulatory requirements and company SOPs.
- Regional travel.
Qualifications :
If you are interested in finding out more about this role or others, please contact Sharleney Chandraratna at schandraratna@i-pharmconsulting.com or call : 44 (0) 2075510732
