What are the responsibilities and job description for the Clinical Trials Management Associate position at ATR International?
We are seeking an experienced Clinical Trials Management Associate to support the planning, coordination, and execution of clinical trials for a high-profile client. This role ensures regulatory compliance, data quality, and efficient collaboration with CROs, vendors, and internal teams.
Responsibilities
- Conduct site evaluations, initiations, monitoring, and close-out visits
- Ensure protocol, regulatory, and data quality compliance
- Support study timelines, project plans, and vendor coordination
- Assist in CRO/vendor selection and oversight
- Draft and review protocols, informed consents, CRFs, and monitoring plans
- Support data review, discrepancy resolution, and study report preparation
- Participate in cross-functional, CRO, and vendor meetings
- Assist in CRA and project assistant training
- Participate in departmental initiatives
- Travel as required
Qualifications
- BS/BA in a scientific field or RN certification with 4 years of clinical research experience
- CCRA or other certification preferred
- Knowledge of FDA/EMEA regulations, ICH-GCP
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong communication, organizational, and problem-solving skills
- Ability to manage multiple priorities and improve project efficiency
Salary : $55 - $65