Senior Clinical Research Coordinator - 255410

Medix™; Denver (CO); On-site; USD 44,000 - 54,000; Full time

Job summary

Medix is seeking an experienced Senior Clinical Research Coordinator to lead oncology trials in Lakewood, CO. The role covers end-to-end study management, protocol adherence, and data integrity, with oversight of informed consent and safety reporting.

Ideal candidates have 3 years of CRC experience, a Bachelor’s degree (ACRP/SOCRA a plus), and strong proficiency in SOP development and Microsoft Office 365.

Qualifications

• 3 years of Clinical Research Coordinating experience, preferably in oncology.
• Bachelor’s degree preferred; industry certification (ACRP/SOCRA) highly desired.

Responsibilities

• Execute study procedures and participant visits ensuring protocol compliance throughout the study lifecycle.
• Maintain accurate source documentation (ALCOA) and eCRFs; manage informed consent and safety reporting (SAEs).
• Serve as a subject matter expert and mentor staff; act as escalation point for complex trial issues.
• Manage participant recruitment and screening to meet sponsor timelines with ethical standards.
• Oversee study materials, lab supplies, and site communications with investigators and sponsors.

Skills

Clinical research

Leadership

Risk assessment

Data management

SOP development

GCP knowledge

Education

Bachelor's degree

Tools

Microsoft Office 365

eCRF systems

Job description

Senior Clinical Research Coordinator Role in Lakewood, CO (80228)

Role Summary

We are seeking an experienced Senior Clinical Research Coordinator (CRC) to lead oncology clinical trials. You will be responsible for end-to-end study management, ensuring strict adherence to protocols, federal regulations, and Good Clinical Practice (GCP) guidelines. This role requires a high level of clinical expertise, strong leadership, and a commitment to maintaining data integrity and participant safety.

Key Responsibilities

• Protocol & Patient Management: Execute all study-related procedures, conduct participant visits, and ensure protocol compliance throughout the study lifecycle.
• Compliance & Documentation: Maintain accurate, real-time source documentation (ALCOA) and eCRFs; manage informed consent and safety reporting (including SAEs) within required timeframes.
• Leadership: Serve as a subject matter expert and mentor for research staff; act as an escalation point for complex trial issues.
• Enrollment: Manage participant recruitment and screening to meet sponsor timelines while upholding medical ethics.
• Operational Oversight: Manage study materials, lab supplies, and site communications with investigators and sponsors.

Qualifications

• Experience: 3 Years of Clinical Research Coordinating experience; Preferably Oncology experience
• Education: Bachelor’s degree preferred; industry certification (e.g., ACRP/SOCRA) is highly desired.
• Skills: Proficiency in clinical research methodology, Microsoft Office 365, and SOP development.
• Competencies: Strong critical thinking, risk assessment, process improvement, and conflict management skills.

Location: Lakewood, CO (80228)

Hours: Monday-Friday; Normal Business Hours; Onsite 5 Days a Week

Pay: $32/hr-$39/hr - Dependent on background and years of experience