Research Coordinator Clinical Trials Specialist
3 weeks ago
Job Summary:
This position will be part of a research team focused on the psychological experiences of a variety of medical conditions, including those admitted to critical care settings and individuals who have sustained traumatic injury.
The Clinical Research Coordinator will assist various Principal Investigators in conducting clinical trials during all phases of trials, including pre-study implementation through study closure, per federal, state, and institutional guidelines.
Key Responsibilities:
- Implement various protocols for assigned research projects, interacting with PIs, clinical managers, and supervisors.
- Creates, facilitates, and/or executes project workflows based on the needs of the clinical trial protocol.
- Ensures appropriate billing or charging mechanisms are in place for research charges related to research studies.
- Performs research subject informed consent and entry into appropriate research studies.
- Partners and coordinates with regulatory compliance, preparing Institutional Review Board (IRB) materials for approval of protocol amendments.
- Obtains knowledge of departmental functions through reading literature, attending workshops, seminars, and conferences.
- Conducts and coordinates study-monitoring visits.
Requirements:
- Research certification or other certifications per specialty area preferred.
- Proven written and oral communication skills.
- Exceptional 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.
Benefits:
- Immediate eligibility for health and welfare benefits.
- 401(k) savings plan with dollar-for-dollar match up to 5%.
- Tuition Reimbursement.
- PTO accrual beginning Day 1.
Qualifications:
- Bachelor's or 4 years of work experience above the minimum qualification.
- Less than 1 Year of Experience.
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