Onsite Clinical Research Assistant — Oncology Trials

Medix™; Southfield (MI); On-site; USD 49,000 - 58,000; Full time

Job summary

Medix seeks a Clinical Research Assistant to support oncology trials at our Denver area clinic. Working under a Clinical Research Coordinator, you will execute protocol procedures, collect accurate data, ensure participant safety, and maintain audit-ready study documentation.

Responsibilities include protocol execution, informed consent, participant recruitment, data entry in CRFs/eCRFs, safety reporting, inventory management, and clear coordination with investigators and sponsors while

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, Healthcare Administration, or related field.
• 1–3+ years in clinical or biological research environments; oncology trials preferred.
• Strong clinical skills including phlebotomy, ECG, and sample handling; proficient in MS Office and eCRF tools.

Responsibilities

• Protocol execution: assist CRCs in subject visits and assessments.
• Informed consent: guide participants per GCP and IRB rules.
• Participant recruitment: identify, screen and enroll eligible candidates.
• Documentation & data management: complete CRFs/eCRFs and record data.
• Safety monitoring: report adverse events and deviations promptly.
• Investigational supplies: oversee inventory and study materials.
• Communication: liaise with investigators, sponsors and review boards.
• Compliance & development: adhere to GCP, SOPs and ongoing training.

Skills

Phlebotomy

ECG acquisition

Sample collection/processing

Education

Bachelor’s degree in Life Sciences, Nursing, Healthcare Administration, or related field

Tools

Microsoft Office 365

eCRF platforms

Job description

Medix seeks a Clinical Research Assistant to support oncology trials at our Denver area clinic. Working under a Clinical Research Coordinator, you will execute protocol procedures, collect accurate data, ensure participant safety, and maintain audit-ready study documentation.

Responsibilities include protocol execution, informed consent, participant recruitment, data entry in CRFs/eCRFs, safety reporting, inventory management, and clear coordination with investigators and sponsors while