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

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