Submission for the position: Clinical Research Coordinator II

2 weeks ago


Plano, Texas, United States Baylor Scott & White Healthcare Full time
Exciting Opportunity in Diabetic Wound Care Study

Location: Plano Clinical Trials Office

ROLE HIGHLIGHTS

The Clinical Research Coordinator 2 plays a crucial role in supporting Principal Investigators (PI) in the seamless execution of clinical trials, ensuring compliance with regulatory guidelines.

PRIMARY RESPONSIBILITIES
  • Collaborate with Study Sponsors, PIs, and clinical managers to assess feasibility of new protocols.
  • Facilitate protocol implementation across various departments and provide education to healthcare professionals.
  • Manage IRB submissions and oversee drug accountability.
  • Create research study budgets and ensure billing compliance.
  • Organize study-monitoring visits and handle invoicing for patient care expenses.
  • Contribute to data analysis and publication of research findings.
  • Establish and enforce Clinical Research policies and procedures.
  • Participate in quality audits to uphold standards.
QUALIFICATIONS
  • Bachelor's degree or equivalent work experience.
  • Minimum of 2 years of relevant experience.
  • Phlebotomy training is a plus.
  • Hold certifications such as CCRA, CCRC, or CCRP-RES within one year.
KEY ATTRIBUTES
  • Strong communication and computer skills.
  • Effective time management and problem-solving abilities.
  • Proven capability to work independently and collaboratively.
  • Experience in managing complex clinical studies.
BENEFITS

Joining our team offers a range of benefits including immediate health coverage, retirement savings plan, tuition reimbursement, and starting PTO accrual from day one.

Note: Benefit eligibility may vary depending on job level and type.

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