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

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