Job Summary
The Clinical Research Associate II plays a vital role in ensuring the smooth operation and efficiency of clinical trials. This position requires a skilled individual who can oversee study sites, manage compliance with regulatory standards, and facilitate communication between all stakeholders involved in the research process. The role emphasizes a hybrid working model, combining both remote and on-site responsibilities depending on study requirements.
Responsibilities
- Monitor clinical trial activities to ensure adherence to protocols and regulations.
- Conduct site evaluations, initiation visits, and routine monitoring visits.
- Maintain meticulous documentation and provide regular updates on trial progress.
- Assist in training site staff and ensure they are well-informed about study protocols.
- Act as a primary liaison between the study sites, sponsors, and other relevant parties.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Previous experience as a Clinical Research Associate, preferably in a hybrid role.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent communication and interpersonal skills.
- Proficiency in data entry and tracking software related to clinical research.
