JOB SUMMARY

The Clinical Research Coordinator 2 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.

ESSENTIAL FUNCTIONS OF THE ROLE

Reviews new protocols and other materials provided by Study Sponsors, and provides input to the PIs and clinical managers, as applicable, regarding clinical and research issues in order to establish financial and clinical feasibility.
Coordinates the implementation of various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors, providing in-service education for healthcare professionals, and working with Pharmacy to ensure a smooth project flow.
Reports to the Institutional Review Board (IRB), completing IRB review reports and assisting with drug accountability.
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.

KEY SUCCESS FACTORS

Research certification and other certifications per specialty area preferred.
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.

BENEFITS

Our competitive benefits package includes the following.

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 - 2 Years of Experience
CERTIFICATION/LICENSE/REGISTRATION - Cert Clinical Research Assoc (CCRA), Cert Clinical Research Coord (CCRC), CCRP-Cert Clnl Research Prof (CCRP-RES): Research Certification and/or certification that pertains to particular work area must be obtained within one year.

Qualifications

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): Research Certification and/or certification that pertains to particular work area must be obtained within one year

Benefits

Our competitive benefits package includes the following
Our benefits are designed to help you live well no matter where you are on your journey
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

Responsibilities

The Clinical Research Coordinator 2 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
Reviews new protocols and other materials provided by Study Sponsors, and provides input to the PIs and clinical managers, as applicable, regarding clinical and research issues in order to establish financial and clinical feasibility
Coordinates the implementation of various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors, providing in-service education for healthcare professionals, and working with Pharmacy to ensure a smooth project flow
Reports to the Institutional Review Board (IRB), completing IRB review reports and assisting with drug accountability
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

Clinical Research Coord 2 Cardiology

Job Type