International Medical Graduate IMG - Clinical Research

Denton, TXFull-timePosted Apr 21, 2026

Behavioral Health Market Context

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•Additionally, someone with a strong interest in the Clinical Research field would be an excellent fit for our entry level position, with room to grow
•International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg
•Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality
•Maintain data integrity within the department
•Must be able to work in a team consisting of physicians, nurses, technicians, secretarial staff and ancillary hospital staff
•Knowledge of FDA Regulations and Good Clinical Practices
•3 more items(s)

•New Staff should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drives productivity and results
•Some responsibilities will include coordinating and managing multiple studies
•They are also responsible for assisting the Principal Investigators and other clinical staff, with any study related tasks as follows but not limited to:
•Research participant screening, recruitment and enrollment
•Consent and conduct research visits for data collection/no risk trials or no study article/minimal risk trials with oversight
•Responsible for collecting, processing and shipping of research specimens, where applicable
•Document study related information in case report forms or electronic data capture systems, handles data queries and participates in monitoring visits
•Obtain, review and maintain source documents
•Maintain organization of all trial related documents and correspondence
•Implement quality control and assurance methods
•Communicate with study sponsors, research team and the Institutional Review Board
•Assist with basic regulatory document preparation, with oversight e.g
•study amendments, adverse event reporting, protocol deviation reporting
•Maintain professional and technical knowledge of Clinical trials and Standards of Care
•Protect patient confidentiality
•12 more items(s)