Submission for the position: Clinical Research Coordinator II
2 weeks ago
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.
- 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.
- 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.
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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