Job Summary
The Clinical Research Associate II plays a vital role in the management and oversight of clinical trials. This position involves ensuring that studies are conducted in compliance with regulatory standards, Good Clinical Practices (GCP), and company policies. The role requires a proactive approach to monitor the progress of trials, address issues as they arise, and facilitate communication among all stakeholders involved in the research process.
Responsibilities
- Oversee the initiation, monitoring, and closure of clinical trials to ensure compliance with protocols and regulatory requirements.
- Conduct regular site visits to assess study progress and address any site-level issues.
- Manage essential documentation and ensure the integrity of data collected during the trials.
- Provide training and guidance to site staff and ensure they adhere to protocols and GCP.
- Collaborate with cross-functional teams, including regulatory affairs and data management, to support the research objectives.
Qualifications
- A Bachelor’s degree in a life science or related field is preferred.
- Experience in clinical research, particularly in monitoring clinical trials, is required.
- Knowledge of regulatory requirements and GCP is essential.
- Excellent organizational and communication skills.
- Ability to work independently and as part of a team in a fast-paced environment.
Kelly 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.
