Company Overview
Advanced Reconstructive Surgery Alliance (ARSA) and its affiliates are the largest Plastic Surgery medical practice in the country. Our expanding team of top tier physicians, coupled with our continued medical advancements, allows us to offer patients extraordinary clinical services with a 5-star experience. We have a bold vision with a desire to revolutionize the industry, meeting patient needs while favorably transforming their lives. Common across the enterprise is not only the commitment to providing safe patient care, but to employee satisfaction and growth opportunities. It is a culture of teamwork, respect and appreciation for all employees-whether caring for patients directly or working in a support role.
Title: Senior Clinical Research Coordinator
ARSA Health is seeking a highly motivated and skilled individual to join our research department as a Senior Clinical Research Coordinator. The successful candidate will be responsible for assisting with various clinical research activities, including overseeing the day-to-day operations of one or more clinical studies, ensuring compliance with protocols, regulations, and ethical guidelines, literature reviews, manuscript writing, and preparing presentations.
Responsibilities:
Overseeing all aspects of the study lifecycle, from start-up to close-out, including protocol preparation, recruitment, and data management
- Study Management:
- Overseeing all aspects of the study lifecycle, from start-up to close-out, including protocol preparation, recruitment, and data management.
- Data Management:
- Ensuring accurate and timely data collection, documentation, and reporting, including adverse event reporting.
- Compliance:
- Maintaining complete and accurate regulatory files, ensuring adherence to GCP guidelines, and addressing queries.
- Supervision and Training:
- May supervise and train other CRCs, providing guidance and support.
- Communication:
- Serving as a liaison between the research team, sponsors, and other stakeholders.
- Project Management:
- Prioritizing tasks, managing budgets, and ensuring timely completion of study milestones.
- Technical Procedures:
- Performing study-specific procedures, such as phlebotomy, ECGs, and vital signs, as required by the protocol.
- Recruitment and Enrollment:
- Developing and executing recruitment plans, screening patients, and obtaining informed consent.
- Regulatory Submissions:
- Assisting with the preparation and submission of regulatory documents, such as IRB applications.
Qualifications:
- Bachelor's degree or equivalent experience in a related field.
- Significant experience in clinical research.
- Strong organizational, analytical, and communication skills.
- Proficiency in relevant software programs, such as electronic data capture systems and data management software.
- Knowledge of GCP guidelines, ethical guidelines, and regulatory requirements for clinical research.
- Ability to work independently and as part of a team.
- The ability to train and mentor other staff.