Clinical Research Specialist Jobs

GENERAL SUMMARY: This position serves to support the migration and transcription of existing clinical research budgets into the Clinical Trial Management System (CTMS). This position requires a working knowledge and understanding of complex budgets and coordination of information between the informed consent, coverage analysis, internal and external budget reports and research contracts.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

§ Create the protocol schedule of events/calendar within the Clinical Trial Management system.

§ Transcribe existing negotiated budgets into the Clinical Trial Management system.

§ Cross-reference the budget with the contract, payment terms, coverage analysis and informed consent to ensure consistency.

§ Set up financial and operational data of clinical studies in the CTMS

§ Other miscellaneous duties as needed.

CRITICAL SKILLS/EXPERTISE:

General knowledge of clinical research administration. Ability to comprehend verbal and written instructions. Excellent communication skills required. Proficiency using Microsoft Office Suite Applications, specifically Excel. Strong organizational skills, ability to read and attend to detail, and manage competing priorities. Ability to work as a team and communicate with a wide range of individuals in a cross-functional environment.

MINIMUM EDUCATION AND EXPERIENCE:

• Two plus years of experience in the academic or pharmaceutical clinical trials environment (preferred). Demonstrated knowledge of budgeting and accounting processes highly desired
• College degree required.

PREFERRED SKILLS/EXPERTISE:

• Experience with cancer protocols.
• Familiarity with OnCore CTMS.