Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in overseeing clinical trials. This position involves managing the interaction between sponsors/CROs and investigative sites, ensuring the integrity of data collected during these studies.
Responsibilities
- Monitor the progress of clinical trials to ensure compliance with regulatory guidelines.
- Act as the primary liaison between the sponsor or contract research organization (CRO) and the investigative sites.
- Ensure the accuracy and integrity of data collected during the trial.
- Conduct site visits and audits to assess procedure compliance.
- Collaborate with investigative teams to address and resolve any issues that arise during the study.
Qualifications
- A degree in life sciences, nursing, pharmacy, or a related discipline.
- Approximately 1 to 3+ years of relevant experience in clinical research.
- Strong understanding of clinical trial protocols and regulatory requirements.
- Excellent communication and interpersonal skills for effective collaboration.
- Ability to work onsite and travel as required for monitoring activities.
allied executive solutions 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.
