Clinical Research Site Manager

Headlands Research; Riverside (CA); On-site; USD 100,000 - 105,000; Full time

Job summary

Headlands Research is seeking a Site Manager for their Riverside, CA location. The role includes overseeing clinical research activities, managing site operations, and ensuring compliance with FDA regulations. Candidates should have 5+ years of clinical trial coordination experience and strong leadership skills.

The Site Manager will lead the site team, ensure successful patient enrollment, and optimize trial processes. A Bachelor's degree is preferred. The position offers a competitive salary range of $100,000 - $105,000 per year.

Qualifications

• 5+ years of experience as a Clinical Research Coordinator on multiple phase 2-4 clinical trials.
• Proficiency in FDA regulations governing clinical trials.
• Knowledge of medical terminology relevant to clinical trials management.

Responsibilities

• Evaluate overall performance of the site and implement improvement processes.
• Hire, train, and manage site staff including Clinical Research Coordinators.
• Ensure site’s compliance with FDA, ICH, and local regulations.
• Monitor study activities to ensure compliance with study protocols.
• Manage patient recruitment and retention efforts.

Skills

Supervisory skills

Communication skills

Knowledge of FDA regulations

Data management

Education

Bachelor's degree

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting‑edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.

The Role

The Site Manager performs clinical research activities as a Clinical Research Coordinator while also serving as Manager of the site operations. The Site Manager owns meeting or exceeding financial targets, KPIs, and patient enrollment, as well as champions screening, patient retention, and partnering with other Headlands centralized departments or sites.

Position Type

Full‑time

Location

Onsite in Riverside, CA

Responsibilities

• Strategic and Operational Management
  • Evaluates overall performance of the Site and recommends and implements processes and plans for improvement.
  • Responsible for maintaining a site calendar to ensure adequate enrollment for studies and coordination of employee PTO.
• Staff Development and Management
  • Fosters a culture of excellence, teamwork, and innovation among site staff.
  • Hires, trains, and mentors site staff, including Clinical Research Coordinators, Research Assistants, Administrative Assistants, Registered Nurses, support personnel, etc.
  • Partners with Human Resources and Management when hiring new employees for the site by reviewing candidate credentials, conducting interviews, and giving input about potential new hires.
  • Supervises performance of other Clinical Research Coordinators, Research Assistants, and support staff at the Site.
• Quality Assurance & Compliance
  • Maintains up‑to‑date knowledge of all relevant regulatory guidelines and requirements.
  • Ensures the site’s compliance with FDA, ICH, and local regulatory agency regulations.
• Clinical Research Coordination
  • Performs the duties of a Clinical Research Coordinator while continuing as Site Manager.
  • Protects the rights, safety, and welfare of human subjects, follows Good Clinical Practice, and works cooperatively with others.
  • Monitors study activities to ensure compliance with study protocols, site policies, and applicable federal, state, and local regulations.
  • Oversees the planning, initiation, and execution of clinical trials at the site.
  • Maintains required records of study activity including case report forms, drug dispensation records, and regulatory forms.
  • Manages and optimizes patient recruitment and retention efforts.
  • Assesses eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and other healthcare professionals.
  • Addresses any patient concerns or issues promptly and professionally.
• Documentation and Reporting
  • Documents findings and events in the CTMS platform and in other binders and platforms as directed.
  • Reviews proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
• Performs other duties as assigned, including those routinely performed by the Company’s Research Assistants.

Requirements

• 5+ years of experience as a delegated Clinical Research Coordinator on multiple phase 2‑4 clinical research trials, simultaneously.
• Proficiency in FDA regulations governing clinical trials.
• Strong supervisory skills to lead research staff effectively.
• Ability to collect and manage research data accurately.
• Familiarity with documentation review processes in clinical research.
• Knowledge of medical terminology relevant to clinical trials management.
• IATA (dangerous goods handling).
• GCP (Good Clinical Practice).
• Strong communication skills with all members of the team.

Preferred Qualifications

• Bachelor’s degree.
• Capability to perform phlebotomy procedures.
• CCRC or CCRP certified.

California Pay Range

$100,000 - $105,000 USD

Equal Opportunity Employment

Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

Accommodations

Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact [e-mail] for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.