Clinical Research Assistant

Medix is recruiting for an unnamed Denver-area clinic seeking a Clinical Research Assistant to support oncology clinical trials. The role assists with study visits, participant consent and recruitment, clinical data and documentation, safety monitoring, and compliance with trial protocols.

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

Preferred

Prior exposure to oncology trials is strongly preferred

Oncology Trials Experience

Company

Medication and health product distribution in Lebanon.

Jdeïdé, Mont-Liban, LBN

https://medixdistribution.com/

Founded in 2007

11-50 employees

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

Practical clinical skills such as phlebotomy, ECG acquisition, and sample collection/processing

Proficiency in Microsoft Office 365 and clinical research software/eCRF platforms

Prior exposure to oncology trials is strongly preferred

1-3+ years of experience in clinical or biological research environments.

Required skills

Represents the skills you have, click on the tags, Phlebotomy, Acquisition, Sample Collection and Processing, Microsoft Office 365

Preferred skills

Prior exposure to oncology trials is strongly preferred, Glassdoor, 4.1, Jdeïdé, Mont-Liban, LBN, https://medixdistribution.com/, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit, Understand your strength & weakness

Experience

1+ years