Clinical Research Assistant

Medix; Lakewood (CO); On-site; USD 50,000 - 58,000; Full time

Job summary

Medix in Lakewood, CO is seeking a Clinical Research Assistant to support oncology clinical trials at our Denver-area clinic. Reporting to the CRC, you will help execute protocol procedures, gather accurate data, and maintain audit-ready study documentation.

The role requires a Bachelor's degree in Life Sciences or related field and 1–3+ years of clinical or biological research experience, preferably oncology.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, Healthcare Administration, or a related field (or equivalent hands-on clinical research experience).
• 1–3+ years of experience in clinical or biological research environments; oncology trials preferred.

Responsibilities

• Protocol Execution: Review and understand study requirements to assist CRCs in conducting subject visits and completing protocol-mandated assessments accurately.
• Informed Consent: Guide study participants through the informed consent process in compliance with GCP, IRB guidelines, and federal rules.
• Participant Recruitment: Help identify, screen, and enroll eligible trial candidates to meet recruitment milestones on schedule.
• Documentation & Data Management: Prepare source documents, complete CRFs/eCRFs, and record clinical observations, lab results, and patient data in alignment with trial protocols.
• Safety Monitoring: Immediately report any adverse events or protocol deviations to the Principal Investigator and Study Coordinator.
• Investigational Supplies: Help oversee inventory and tracking of clinical trial materials, including laboratory supplies, documentation, and study products.
• Communication & Professionalism: Maintain clear, compliant communication with investigators, study sponsors, review boards, and multidisciplinary healthcare teams.
• Compliance & Development: Adhere to GCP, IRBs, SOPs, and ethical guidelines while engaging in ongoing professional development.

Skills

Phlebotomy

ECG acquisition

Data collection

Documentation

Education

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

Tools

Microsoft Office 365

Clinical research software/eCRF

Job description

Clinical Research Assistant (259007) Lakewood, Colorado

Salary: USD24 - USD28 per hour

Clinical Research Assistant in Denver Area (80228)

Summary

We are seeking a dedicated Clinical Research Assistant (RA) to support oncology clinical trials at our Denver clinic. Operating under the direction of a Clinical Research Coordinator (CRC), the RA plays a critical role in executing protocol procedures, gathering clean and precise clinical data, ensuring participant safety, and maintaining audit-ready study documentation.

Responsibilities

• Protocol Execution: Review and understand study requirements to assist CRCs in conducting subject visits and completing protocol-mandated assessments accurately.
• Informed Consent: Guide study participants through the informed consent process in compliance with GCP, IRB guidelines, and federal rules.
• Participant Recruitment: Help identify, screen, and enroll eligible trial candidates to meet recruitment milestones on schedule.
• Documentation & Data Management: Prepare source documents, complete Case Report Forms (CRFs/eCRFs), and record clinical observations, lab results, and patient data in alignment with trial protocols.
• Safety Monitoring: Immediately report any adverse events or protocol deviations to the Principal Investigator and Study Coordinator.
• Investigational Supplies: Help oversee inventory and tracking of clinical trial materials, including laboratory supplies, documentation, and study products.
• Communication & Professionalism: Maintain clear, compliant communication with investigators, study sponsors, review boards, and multidisciplinary healthcare teams.
• Compliance & Development: Adhere strictly to Good Clinical Practice (GCP), local IRBs, standard operating procedures (SOPs), and ethical guidelines while engaging in ongoing professional development.

Qualifications

Education

• Bachelor’s degree in Life Sciences, Nursing, Healthcare Administration, or a related field (or equivalent hands‑on clinical research experience).

Experience

• 1–3+ years of experience in clinical or biological research environments. Prior exposure to oncology trials is strongly preferred.

Skills and Competencies

• Practical clinical skills such as phlebotomy, ECG acquisition, and sample collection/processing.
• Proficiency in Microsoft Office 365 and clinical research software/eCRF platforms.

Location

Lakewood, CO (80228)

Hours

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

Pay

$24/hr-$28/hr ($49,000-$58,000 Annual Salary) - Dependent on background and years of experience

Employment

Direct Hire