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Clinical Research Site Director

Clinical Research Site Director

C-Clinical at Los AngelesLos Angeles, CA, US
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Job Description

Job Description

Clinical Research Site Director – Oncology

A leading hematology and oncology research facility in Los Angeles is seeking a Clinical Research Site Director to take charge of daily operations and guide the delivery of innovative cancer trials. This is a rare opportunity to influence breakthrough therapies and play a vital role in advancing patient care on a global scale.

In this leadership position, you will oversee clinical staff, build and maintain sponsor relationships, and ensure that every trial is executed with precision and integrity. Your expertise in oncology research and command of regulatory standards (FDA / 21 CFR and ICH-GCP) will set the standard for quality and compliance across the site.

We are looking for a leader with hands-on oncology trial experience, a proven record in clinical operations, and the ability to cultivate strong, motivated teams. The ideal candidate thrives in complex environments, balancing operational efficiency with the compassion required in cancer research.

What You’ll Do :

  • Direct day-to-day site operations and provide oversight to research teams
  • Collaborate with sponsors to meet study goals, budgets, and timelines
  • Maintain full compliance with regulatory and ethical requirements
  • Enhance participant care, satisfaction, and retention strategies
  • Track performance indicators and implement solutions for continuous improvement

If you’re ready to lead a research site dedicated to oncology and hematology advancement, this is your chance to have a direct impact on the future of cancer care. Apply today and join a mission that saves lives.

Compensation : $145,000 - $165,000

Responsibilities :

  • Site Management : Oversee daily operations of the clinical research site, including study planning, protocol implementation, patient recruitment, data collection, and maintaining regulatory compliance.
  • Team Leadership : Manage and mentor a team of approximately 15 Clinical Research Coordinators and 10+ Research Assistants. Provide guidance and training and conduct performance evaluations to ensure high-quality work and adherence to compliance standards.
  • Regulatory Compliance : Ensure all clinical research activities comply with Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and other relevant regulatory requirements.
  • Study Execution : Serve as the subject matter expert for sponsors and research organizations, collaborating with the Principal Investigator (PI) to oversee compliance of clinical trial teams in accordance with protocols, timelines, and budgets.
  • Patient Recruitment & Retention : Work closely with the recruitment team to develop effective strategies for research participant recruitment and retention, ensuring access to eligible participants and maintaining participant engagement throughout the study.
  • Budget & Financial Oversight : Manage study budgets, invoicing, and site expenditures, ensuring effective use of resources while staying within allocated financial parameters.
  • Quality Assurance : Ensure data integrity by reviewing audit trails, identifying compliance or quality concerns, and implementing corrective actions. Monitor ongoing site performance to detect risks and take proactive measures.
  • Collaboration & Communication : Foster strong communication and collaboration between internal teams, study sponsors, and external stakeholders, ensuring alignment and transparency in the study’s progress.
  • Clinical Data Management : Oversee the collection and review of clinical data, ensuring strict compliance with study protocols and regulatory requirements.

    • Qualifications :

  • Education : Bachelor's degree in life sciences, nursing, or a related field (required). A Master's degree or higher is preferred.
  • Experience : Minimum of 5 years of clinical research experience, with at least 2 years in hematology / oncology clinical trials. A minimum of 3 years in a management or leadership role overseeing clinical research teams (CRCs and RAs).
  • Certifications : CCRP (Certified Clinical Research Professional), CCRC (Certified Clinical Research Coordinator), or other relevant certifications preferred.
  • Knowledge : In-depth understanding of clinical research methodologies, regulatory compliance (FDA, ICH-GCP), and hematology / oncology drug development.
  • Skills : Strong leadership, communication, organizational, and problem-solving skills. Proficiency in clinical trial management systems and Microsoft Office Suite.
  • Other : Ability to manage multiple priorities in a fast-paced environment while maintaining high standards of performance and patient care.

    • Compensation : The salary for this position is competitive and positioned within the 80th to 90th percentile for Clinical Research Site Directors in the Los Angeles area, based on experience and qualifications. A comprehensive benefits package is included, covering health, dental, and vision insurance, 401(k), and paid time off.

    Work Environment :

  • The Clinical Research Site Director will primarily work in a clinical research setting, interacting with patients, site staff, and external stakeholders.
  • Occasional travel to sponsor meetings or other clinical sites may be required.
  • Full-time position with flexible hours based on study needs.

    • About Company

    C-Clinical in Los Angeles drives clinical operations excellence across the pharmaceutical, biotechnology, and device sectors.

    Our chief concept is in guiding relationships and directing the government. We go by "love" in the principle : love your neighbor as yourself, and charity.

    C-Clinical was not an act of compulsion, but the care one would have for family.

    Bottom line - we created this company to do what we love to do : life-changing medical research, and to dedicate our time, talents, and resources to those who need them.

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    Director Research • Los Angeles, CA, US

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