Clinical Research Assistant - 259007

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

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