Clinical Research Coordinator (CRC)

Type of Requisition

Regular

Clearance Level Must Currently Possess

None

Clearance Level Must Be Able to Obtain

None

Public Trust/Other Required

NACLC (T3)

Job Family

Science and Research

Job Qualifications

Skills: Clinical Research, Informed Consent, IRB (Inactive), Participant Recruiting Certifications: None Experience: 3 + years of related experience US Citizenship Required: No

Job Description

GDIT's Military Health Team is hiring a Clinical Research Coordinator (CRC) to join our current research team to help carry out Traumatic Brain Injury Research for the Traumatic Brain Injury Center of Excellence (TBICoE) located at Ft. Bragg in Fayetteville, North Carolina.

MISSION

TBICoE unifies a system of TBI health care, reliably advancing the science for the warfighter and ready to meet future brain health challenges Learn more about the mission HERE

HOW YOU WILL MAKE AN IMPACT

• The CRC is responsible for coordinating and assuring integrity of all activities associated with conducting TBICoE clinical investigations in the area of TBI.
• S/he will ensure compliance with local, state, and/or federal regulatory requirements.
• Assists Principal / Associate Investigators in the preparation and submission of clinical protocols, consent forms and other documents to the scientific review committee, IRB and other regulatory organizations.
• Prepares requests for actions/proposals to include assisting with and providing coordination for grant proposal applications and their associated documentations and requirements as needed.
• Facilitates the flow and approval processes for relevant projects as needed or requested.
• Maintains regulatory files related to TBICoE clinical investigations.
• Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management and outside collaborators.
• Recruits, interviews, and screens TBICoE clinical research study volunteers, administers and obtains informed consent.
• Assists in the collection and analysis of data to evaluate volunteer eligibility for enrollment.
• May assist with TBI Program/Quality Improvement initiatives at their site.
• Assists in the collection, analysis and interpretation of laboratory and clinical data obtained during a medical evaluation, report significant values, findings and events that require prompt attention to clinical investigators.
• Assists with the documentation and reporting of adverse events, completes and reviews subject eligibility criteria, protocol compliance, omissions, and errors and submits these forms as required.
• Prepares and maintains written and electronic volunteer databases/logs.
• Performs data extraction and chart reviews of patients’ and/or research participant’s medical records or other relevant record/systems, as applicable.
• Ensures that research records are stored and secured properly and that inventory and records are updated and properly maintained.
• Conducts data verification as indicated, documents, assists the investigator and protocol coordinator with questions, may transcribe and resolve queries of data on study forms (hardcopy and/or electronic).
• Prepares documents, under direction of project leads.
• Trains incoming staff on study procedures and SOPs.
• Assists with statistical analyses and descriptive data capture under direction of project leads.
• Works with the site senior clinical research director and other senior research leads for the collection, documentation and analysis of metrics to ensure a successful research program.
• Must adhere to legal, professional and ethical codes with respect to confidentiality and privacy.
• US citizenship with the ability to pass a T3 security investigation.

WHAT YOU'LL NEED TO SUCCEED (REQUIRED)

• Bachelor's degree or higher in biology, psychology or related science.
• Must have Human Subjects training completed.
• 3+ years clinical investigations experience.
• Knowledge of standard qualitative and quantitative data collection techniques.
• Good writing and analytical skills familiarity with social science research methodology.
• Ability to work comfortably with computer software, including Microsoft Word, Excel, Outlook and PowerPoint.

WHAT WOULD BE EVEN BETTER (PREFERRED)

• Master’s degree preferred.
• Certification as a Clinical Research Coordinator (CCRC), Clinical Research Professional (CCRP) and/or Clinical Research Associate (CCRA) preferred (must maintain Continuing Education credit sufficient to maintain certification when applicable).
• Prior experience within the DoW/VA systems of care preferred.

SKILLS & ATTTIBUTES FOR SUCESS

• Excellent communication skills, basic clinical acumen, knowledge of universal precautions, organizational skills and proficiency in research conduct.
• Ability to follow general instructions; work in a team environment.

ENVIRONMENTAL DETAILS

Must be able to sit and stand for long periods of time. May encounter patients who are confused, agitated, or abusive. Office and clinical environment.

Job Details

• Job has likely salary range $57,824 - $78,200.
• Scheduled Weekly Hours: 40.
• Travel Required: None.
• Telecommuting Options: Onsite.
• Work Location: USA NC Fort Bragg.
• Additional Work Locations:

Benefits

• Medical plan options, some with Health Savings Accounts, dental plan options, a vision plan, and a 401(k) plan offering the ability to contribute both pre and post-tax dollars up to the IRS annual limits and receive a company match.
• Full flex work weeks where possible and a variety of paid time off plans, including vacation, sick and personal time, holidays, paid parental, military, bereavement and jury duty leave.
• Short and long-term disability benefits, life, accidental death and dismemberment, personal accident, critical illness and business travel and accident insurance.

Our Identity Verification Process

As part of the hiring process, we will ask you to complete an identity verification process that leverages advanced biometrics and artificial intelligence to ensure authenticity and protect against identity fraud. You are expected to be on camera during virtual interviews. We reserve the right to take your picture to verify your identity and prevent fraud. By proceeding, you authorize the collection, processing, and use of your biometric data for identity verification and security purposes.

About Our Work

We are GDIT. A global technology and professional services company that delivers technology solutions and mission services to every major agency across the U.S. government, defense and intelligence community. Our 26,000 experts extract the power of technology to create immediate value and deliver solutions at the edge of innovation. We operate across 50+ countries worldwide, offering leading mission-ready capabilities in AI, cloud, cyber and software development. Join our Talent Community to stay up to date on our career opportunities and events at gdit.com/tc.

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