Clinical Research Coordinator II - Rehab

Baylor Scott & White Health•Irving, TX

3d•Onsite

About The Position

The Clinical Research Coordinator II - Rehab helps Principal Investigators conduct clinical trials. This includes all phases from pre-study implementation to study closure, following federal, state, and Institutional guidelines.

Requirements

Proven written and oral communication skills.
Proven computer skills, including Microsoft Office.
Ability to manage time reactive projects in order to meet deadlines.
Exceptional ability to establish and maintain effective working relationships.
Ability to autonomously operationalize and coordinate large or complex studies from start to finish.
Ability to autonomously work across functional departments within BSWRI.
Proven critical thinking and problem-solving skills; ability to troubleshoot study challenges.
Ability to work within a team, including training of junior staff.
EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification
EXPERIENCE - 2 Years of Experience
CERTIFICATION/LICENSE/REGISTRATION - Cert Clinical Research Assoc (CCRA), Cert Clinical Research Coord (CCRC), CCRP-Cert Clnl Research Prof (CCRP-RES): Obtain research certification related to your work area within one year.

Nice To Haves

Research certification and other certifications per specialty area preferred.
Experience working on Investigator Initiated studies is a plus.

Responsibilities

Reviews new protocols and materials from Study Sponsors. Provides input to PIs and clinical managers on clinical and research issues. Establishes financial and clinical feasibility.
Coordinates research project protocols with departments by interacting with PIs, clinical managers, and supervisors. Provides in-service education for healthcare professionals. Works with Pharmacy to ensure smooth project flow.
Coordinates with the Institutional Review Board (IRB) and completes IRB review reports.
Develops research study budgets for new clinical trials and assists in the completion of all applicable research billing compliance procedures.
Coordinates study-monitoring visits. Completes and submits monthly invoices for applicable patient care charges covered by funded research studies.
Participates in data testing, writing and submitting manuscripts and abstracts for publication, as appropriate.
Develops, implements and administers Clinical Research policies and procedures.
Unites with quality audits.