Details:
- Compensation: $75 - $90k
- Benefits: Medical, Dental, Vision
- Employment Classification: Direct Hire
- Status: On-Site
- Job ID: 21147
Job Title: Clinical Research Site Director
Work Location: Potter County, Texas
Summary:
The Clinical Research Site Director is responsible for leading clinical research operations at the site level, ensuring the successful execution of industry-sponsored clinical trials. This role requires strong leadership, patient care expertise, and a commitment to regulatory compliance and protocol adherence.
Responsibilities:
- Lead and oversee all aspects of clinical trial operations, including patient identification, screening, randomization, and enrollment.
- Coordinate and conduct clinic visits, ensuring high-quality patient care and adherence to study protocols.
- Perform and assist with direct patient care activities such as consenting, physical assessments, blood draws, medication administration, and ECGs.
- Maintain accurate and compliant data entry, regulatory documentation, and study records for efficient site visits and audits.
- Communicate effectively with research teams, principal investigators, sponsors, and monitors to foster strong working relationships.
- Ensure compliance with all applicable laws, regulations, and requirements from governing bodies throughout the study lifecycle.
- Utilize provided technologies to enhance daily operations and support efficient study set-up and maintenance.
- Manage multiple protocols simultaneously, including resolving IRB responses, tracking adverse events, and maintaining eSource materials.
Qualifications:
- Minimum of 5 years of experience coordinating industry-sponsored clinical trials.
- Prior experience in site leadership or management within clinical research.
- Demonstrated expertise in conducting IRB-approved clinical trial protocols and direct patient care activities.
- Strong attention to detail for data entry, regulatory compliance, and protocol adherence.
- Excellent communication and interpersonal skills to build relationships with research teams and stakeholders.
- Ability to manage multiple studies and tasks simultaneously while maintaining focus and accuracy.
- Experience or interest in therapeutic areas such as Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and/or Oncology.
- Commitment to core values such as compassion, integrity, collaboration, innovation, and dedication.
Published Category: Clinical Operations & Development