Job Summary
The Clinical Research Associate II plays a pivotal role in coordinating and overseeing clinical trial activities. This position is vital for ensuring that research projects are executed in compliance with regulatory standards and protocols. The associate will collaborate with cross-functional teams to facilitate the efficient conduct of clinical studies.
Responsibilities
- Monitor the progress of clinical trials to ensure adherence to study protocols and regulatory requirements.
- Conduct site visits and inspections to evaluate investigator performance and ensure data integrity.
- Assist in the preparation of trial documentation, including informed consent forms and study reports.
- Facilitate communication between sites, sponsors, and key stakeholders.
- Provide training and support to site staff regarding study procedures and requirements.
- Collect, analyze, and report data findings to facilitate timely project decisions.
- Participate in the development and implementation of study-related materials and processes.
Qualifications
- Bachelor’s degree in life sciences or a related field; advanced degree preferred.
- Minimum of 2 years of experience in clinical research or related fields.
- Strong understanding of clinical trial methodologies and regulatory guidelines.
- Excellent organizational and communication skills, with attention to detail.
- Ability to work collaboratively within a team and independently manage multiple trial sites.
- Proficiency in data management systems and software for tracking clinical trial progress.
ICON plc provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
