Details:
- Compensation: $90 - $110k
- Benefits: Medical, Dental, Vision
- Employment Classification: Direct Hire
- Status: On-Site
- Job ID: 21148
Job Title: Clinical Research Site Director
GMC Clinical Research
Work Location: Sacramento County, California
Summary:
Seeking an experienced Clinical Research Site Director to lead and coordinate clinical trial activities, ensuring high-quality patient care and regulatory compliance. The ideal candidate will have a strong background in site leadership and clinical trial coordination, with a passion for advancing new therapies and improving patient outcomes.
Responsibilities:
- Lead and oversee all aspects of clinical trial protocols, including patient identification, screening, randomization, and enrollment.
- Supervise and assist with direct patient care activities such as consenting, physical assessments, blood draws, medication administration, and ECGs.
- Ensure accurate data entry, regulatory compliance, and strict adherence to study protocols and governing regulations.
- Maintain productive site visits, efficient study set-up, and ongoing study maintenance.
- Foster effective communication and relationships among research teams, principal investigators, sponsors, and monitors.
- Manage multiple protocols simultaneously, including resolving IRB responses, tracking adverse events, and maintaining eSource materials.
- Utilize provided technologies to enhance daily operations and improve study outcomes.
- Demonstrate ownership of assigned studies and patients, ensuring timely and effective communication with leadership and team members.
Qualifications:
- Minimum 5 years of experience coordinating industry-sponsored clinical trials.
- Prior experience in site leadership or management roles.
- Proficiency in all aspects of IRB-approved clinical trial protocols.
- Skilled in direct patient care activities, including consenting, assessments, and clinical procedures.
- Strong attention to detail for data entry, regulatory compliance, and protocol adherence.
- Excellent communication and relationship-building skills with research teams and external partners.
- Ability to manage multiple studies and tasks simultaneously with focus and efficiency.
- Demonstrated leadership, teamwork, and commitment to advancing clinical research.
Published Category: Clinical Operations & Development