Clinical Research Coordinator

Nuvance Health; Plano (TX); On-site; USD 50,000 - 65,000; Full time

Job summary

A leading health system in Texas seeks a Clinical Research Coordinator I to assist in conducting clinical trials. The role involves implementing protocols, ensuring compliance with regulations, and coordinating with Principal Investigators. Candidates should possess strong communication skills and foundational research knowledge.

Benefits

401(k) savings plan

Tuition Reimbursement

PTO accrual beginning Day 1

Qualifications

• Research certification preferred.
• Less than 1 year of experience highly preferred.

Responsibilities

• Implements protocols for research projects.
• Performs informed consent and entry into studies.
• Conducts audits and quality checks of research studies.

Skills

Communication

Critical Thinking

Detail Orientation

Education

Bachelor's degree or 4 years of work experience

Tools

Microsoft Office

Job description

Description

*JOB SUMMARY* The Clinical Research Coordinator I assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementation through study closure per federal, state and Institutional guidelines. This position will learn to assist Principal Investigators on more complex studies and seek guidance from more senior roles when needed. *ESSENTIAL FUNCTIONS OF THE ROLE* * Implements various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors. * Creates, facilitates, and/or executes a variety of different project workflows based on the needs of the clinical trial protocol. Examples of workflows include, providing in-service education for healthcare professionals and working with Pharmacy to ensure a smooth project flow. * Ensures that appropriate billing or charging mechanisms are in place for research charges related to research studies. Requires familiarity with research study budgets and provides feedback on budgets for new clinical trials. * Performs research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met. * Partners and coordinates with regulatory compliance including preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety forms. Ensures that all study documents are complete and that records are retained per federal, state and institutional standards. * Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations. * Conducts and coordinates study-monitoring visits. Conducts audits and quality checks of research studies to check the accuracy, integrity and consistency of research studies. *KEY SUCCESS FACTORS* * Research certification or other certifications per specialty area preferred. * Strong written and oral communication skills. Provide PIs with concise and clear email communication. * Strong critical thinking skills and foundational research knowledge * Exceptional computer skills, including Microsoft Office. * Ability to manage time reactive projects in order to meet deadlines. * Detail oriented and ability to multi-task in a fast paced environment with standing priorities. * Exceptional ability to establish and maintain effective working relationships. * Travel to McKinney clinic and potential travel to Frisco and Dallas * Phlebotomy experience required for this role * CCRC certification preferred * Strong ability to establish and maintain effective working relationships with PIs, sponsors and colleagues. Meet with PIs regularly (as appropriate) for study questions, obtain signatures and complete required research documentation. * 1 year of coordinator experience highly preferred *BENEFITS* Our benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include: * 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 Note: Benefits may vary based upon position type and/or level *QUALIFICATIONS* - EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification - EXPERIENCE - Less than 1 Year of Experience

As the largest not-for-profit healthcare system in Texas and one of the largest in the United States, Baylor Scott & White Health was born from the 2013 combination of Baylor Health Care System and Scott & White Healthcare.Today, Baylor Scott & White includes 52 hospitals, more than 1,300 health system care sites, more than 7,200 active physicians, over 57,000 employees and the Baylor Scott & White Health Plan.

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