Clinical Research Coordinator II

CAMRIS • San Diego, CA

1d

About The Position

CAMRIS seeks a Clinical Research Coordinator II to support the Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate by overseeing and administering research studies and ensuring compliance with study protocols and regulatory requirements. The role involves assisting with planning, recruiting, and coordinating research subjects, as well as serving as a primary liaison for projects, along with the principal investigator (PI). The Clinical Research Coordinator II oversees staff services, maintains record-keeping systems, and ensures seamless study operations. This position provides an exciting opportunity to lead critical research initiatives in infectious diseases, supporting military health and global public health efforts. The Clinical Research Coordinator II will help ensure the success of clinical trials and research projects at NHRC.
The OID Directorate conducts ongoing, laboratory-based surveillance of US military populations in unique environments to quantify and study the etiology of infectious illnesses. Test specimens are collected from ongoing surveillance programs and from special investigations of febrile illnesses and pneumonia among military personnel or civilians (recruits, forces afloat, deployed forces, outbreaks of concern, and border populations). In addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted. Results are provided to sponsors, local investigators and collaborators, and, when applicable, county health units to guide proper responses that ultimately affect both the readiness of US forces and the safety of public health.

Requirements

• US Citizenship and the ability to obtain and maintain a T3/Secret Clearance.
• A BA/BS in sciences, public health, epidemiology or equivalent PLUS one to two years of clinical research and management experience OR 8+ years of research experience, including two years of research management experience.
• Familiarity with surveillance-based research, IRB submissions and reporting processes.
• Strong understanding of research principles, study design, and regulatory requirements.
• Familiarity with/electronic IRB (eIRB) systems.
• Proactive problem-solving skills, organizational, communication, and leadership skills.
• Ability to work both independently and collaboratively in a research setting.
• Ability to manage multiple projects and prioritize tasks in a dynamic research environment.
• Ability to work in a fast-paced environment and able to balance completing priorities and deadlines.
• Ability to present studies to collaborators and staff.

Nice To Haves

• Familiarity with Tableau and Power BI experience is desired.
• Experience with infectious disease studies or military health research.
• Proven experience in supervisory roles within clinical and surveillance studies.

Responsibilities

• Study Administration and Oversight: Lead research studies and associated activities to ensure adherence to study protocols, timelines, and regulatory standards.
• Monitor, record, and report study progress in close coordination with the PI and study team and assist in study planning to meet milestones and objectives.
• Ensure pre-established work scope and study protocols are followed throughout the study lifecycle.
• Regulatory Compliance: Ensure all activities comply with Institutional Review Board (IRB) requirements and other regulatory standards.
• Prepare, obtain, and track agreements and approvals.
• Prepare and submit IRB applications, amendments, and continuing reviews.
• Maintain accurate study documentation and ensure that study protocols are adhered to throughout the study lifecycle.
• Prepare for and participate in monitoring visits, audits, and inspections by regulatory agencies.
• Participant Recruitment and Coordination: May recruit, screen, and coordinate research subjects as per study protocols.
• May obtain informed consent and schedule subject visits.
• Ensure compliance with study requirements.
• Frequent and clear communication with sites to ensure all aspects of the study are communicated and the sites remain engaged.
• Liaison and Communication: Serve as the primary administrative point of contact between investigators, research staff, and external stakeholders.
• Facilitate communication between clinical teams, sponsors, and regulatory authorities to ensure smooth study execution.
• Administration and Staff Services: Serve as an administrative point of contact between investigators, research staff, and external stakeholders.
• Facilitate communication between study teams, sponsors, and regulatory authorities to ensure smooth study execution.
• Sample Collection, Data Management, and Reporting: Monitor studies to ensure samples are collected per study requirements.
• Supervise data collection and entry to ensure accuracy and completeness.
• Address data queries and resolve discrepancies in accordance with Good Clinical Practice (GCP) guidelines.
• Prepare regular progress reports and assist with study-related presentations.
• Perform other duties as assigned.

Benefits

• CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level