Clinical Research Coordinator – DoD/Government Trials

Talentify; Marine Corps Base Camp Lejeune (NC); On-site; USD 52,000 - 62,000; Full time

Job summary

Bering-Alaka`ina Holdings, LLC is seeking a Clinical Research Coordinator to support government contracts at Camp Lejeune, North Carolina. The role involves designing research protocols, managing IRB and PRB submissions, recruiting subjects, and coordinating study procedures in a DoD context.

Responsibilities include literature reviews, participant recruitment, data entry, and maintaining accurate records while ensuring compliance with HIPAA/PHI/PII and federal regulations.

Qualifications

• Bachelor’s degree in speech and hearing sciences, brain and cognitive sciences, audiology, engineering, or related field.
• At least two years of related research experience in a regulated laboratory.
• Experience with IRB submissions.
• Ability to perform administrative tasks and follow DoD and Federal regulations.
• Excellent communication and analytical skills; ability to meet deadlines.
• Knowledge of HIPAA/PHI/PII and patient confidentiality.
• English proficiency for communication with patients and providers.
• Familiarity with record-keeping and medical terminology in Audiology/SLP.

Responsibilities

• Assist in literature reviews and protocol development.
• Oversee participant recruitment and consent.
• Perform data entry and maintain records, inventories, and logbooks.
• Assist in complex, non-standard tests and data collection procedures.
• Ensure adherence to legal, professional, and ethical codes with respect to privacy.

Skills

IRB submissions

Regulatory compliance

Data entry/record-keeping

Clinical communication

Teamwork

Medical terminology

Education

Bachelor’s degree in related field

Job description

Bering-Alaka`ina Holdings, LLC is seeking a Clinical Research Coordinator to support government contracts at Camp Lejeune, North Carolina. The role involves designing research protocols, managing IRB and PRB submissions, recruiting subjects, and coordinating study procedures in a DoD context.

Responsibilities include literature reviews, participant recruitment, data entry, and maintaining accurate records while ensuring compliance with HIPAA/PHI/PII and federal regulations.