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
Pay: $90,000 - $120,000/year
Location: Onsite in Kelowna, BC
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
In addition to assuming management responsibilities as a Site Manager, this individual performs the duties of a Clinical Research Coordinator
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, with site policies, and with applicable federal, state, and local regulations
Oversee 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 duties 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
