Senior Oncology Clinical Research Lead (Onsite)

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

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.