Clinical Research Assistant (human subject research / TBI)

General Dynamics Information Technology

1d•Onsite

About The Position

GDIT’s Military Health Team is hiring a Clinical Research Assistant to support clinical investigations for the TBI Center of Excellence (TBICoE) located at Ft. Bragg in Fayetteville, North Carolina. As the TBI Pathway of Care manager within the MHS, the Traumatic Brain Injury Center of Excellence promotes state-of-the-science care from point-of-injury to reintegration for service members, veterans, and their families to prevent and mitigate consequences of mild to severe TBI. The Clinical Research Assistant is responsible for assisting with the performance of clinical research projects in a clinical or field based operational setting, including recruitment of potential study subjects, collection of data using psychometric and neuropsychometric tools, data scoring and entry, and scheduling participants for follow up appointments.

Requirements

Bachelor’s Degree required.
1+ year of experience in research/clinical investigations/studies required.
Human Subjects training required.
Current certification in Basic Life Support (BLS).
Ability to pass a T3 security investigation.
Ability to follow detailed instructions required.
Excellent communication and analytical skills required.
Adhere to legal, professional and ethical codes with respect to confidentiality and privacy.

Nice To Haves

Prior experience within the DoW/VA systems of care strongly preferred.
Experience using psychometric and neuropsychometric assessment tools, data scoring and entry.

Responsibilities

Recruits, screens, and consents research participants.
Performs data collection, organization, and entry for clinical investigation projects.
Performs data collection and entry quality checks and quality assurance.
Maintains study related documents and supplies; secures, organizes and documents following all federal/ state regulations.
Creates, collects, disseminates, maintains appropriate files of study data, and assists with review and completion of study manuals and SOPs.
Schedules potential research participants for testing or evaluation.
Completes protocol-specific testing and evaluation requirements.
Facilitates follow-up assessment reminders and scheduling.
Extracts data from patient medical records; transcribes and resolves data queries in case report forms (hardcopy or electronic); prepares documents, under direction of project leaders; reports statistical analyses and descriptive data from patient's study books to be used in research/clinical investigations/studies reports.
Maintains awareness and compliance of research regulatory issues.
Provides written and verbal updates to senior staff.
Communicates regularly with study team, under direction of project leaders, via email and conference calling as needed.
May assist with TBI program/project improvement initiatives at the site
Assists with literature searches and/or obtaining and collating materials for reports, manuscripts, and meetings.
Other duties consistent with the above responsibilities.

Benefits

401K with company match
Comprehensive health and wellness packages
Internal mobility team dedicated to helping you own your career
Professional growth opportunities including paid education and certifications
Cutting-edge technology you can learn from
Rest and recharge with paid vacation and holidays
A variety of medical plan options, some with Health Savings Accounts
Dental plan options
A vision plan
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
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