Medix™
Clinical Research Recruiter | Life Sciences
Location:
Englewood, CO
Schedule:
M-F 8:00 AM - 5:00 PM
Job Type:
Full-Time
Are you passionate about advancing clinical research and supporting the successful execution of clinical trials? We are seeking a detail-oriented
Clinical Research Assistant
to provide direct support to Clinical Research Coordinators (CRCs) and ensure the smooth, efficient, and compliant conduct of clinical studies. This role is ideal for someone who thrives in a fast‑paced research environment and values teamwork, quality, and professional growth.
Key Responsibilities
Create and maintain patient charts for assigned studies.
Prepare participant visits based on CRC schedules, ensuring all source documents, assessments, lab kits, and visit materials are accurate and ready.
File lab results, EKG results, and other documentation into designated patient charts.
Maintain inventory of study‑specific supplies, including lab kits and participant‑facing materials.
Complete data entry and resolve queries for all CRFs within sponsor‑defined timelines.
Assist with participant assessments (e.g., blood pressure, urine collection).
Communicate with study participants, caregivers, third‑party vendors, and labs as needed.
Support Coordinators with scheduling, copying, faxing, and other administrative tasks.
Complete daily tasks delegated by CRCs related to studies or participants.
Perform other duties as assigned in support of study operations.
About the Organization This role is part of a network of highly respected clinical research centers specializing in
Phase I–IV clinical trials . Our sites conduct research across multiple therapeutic areas, including Psychiatry, Acute Post‑Op Pain, Asian Bridging, Dermatology, Gastroenterology, and Neurology. Many of our locations offer in‑patient capabilities and have extensive experience managing complex early‑phase studies.
We prioritize a collaborative and supportive work environment with an emphasis on quality, teamwork, and professional development.
Benefits Full‑time employees are eligible for a competitive compensation package and comprehensive benefits after 30 days of employment, including:
Long‑Term & Short‑Term Disability
Life Insurance
401(k)
Positive workplace culture that emphasizes work‑life balance and strong leadership
Required Skills & Qualifications
Interest in and knowledge of clinical research or specific study indications
Excellent computer skills and proficiency with email, electronic systems, and office equipment
Strong organizational skills and attention to detail
Ability to maintain effective working relationships with supervisors and colleagues
Strong personal initiative and ability to work independently
Ability to stay calm and effective in emergency or high‑pressure situations
Ability to interpret, adapt, and apply guidelines and procedures
Strong verbal and written communication skills
#J-18808-Ljbffr
Englewood, CO
Schedule:
M-F 8:00 AM - 5:00 PM
Job Type:
Full-Time
Are you passionate about advancing clinical research and supporting the successful execution of clinical trials? We are seeking a detail-oriented
Clinical Research Assistant
to provide direct support to Clinical Research Coordinators (CRCs) and ensure the smooth, efficient, and compliant conduct of clinical studies. This role is ideal for someone who thrives in a fast‑paced research environment and values teamwork, quality, and professional growth.
Key Responsibilities
Create and maintain patient charts for assigned studies.
Prepare participant visits based on CRC schedules, ensuring all source documents, assessments, lab kits, and visit materials are accurate and ready.
File lab results, EKG results, and other documentation into designated patient charts.
Maintain inventory of study‑specific supplies, including lab kits and participant‑facing materials.
Complete data entry and resolve queries for all CRFs within sponsor‑defined timelines.
Assist with participant assessments (e.g., blood pressure, urine collection).
Communicate with study participants, caregivers, third‑party vendors, and labs as needed.
Support Coordinators with scheduling, copying, faxing, and other administrative tasks.
Complete daily tasks delegated by CRCs related to studies or participants.
Perform other duties as assigned in support of study operations.
About the Organization This role is part of a network of highly respected clinical research centers specializing in
Phase I–IV clinical trials . Our sites conduct research across multiple therapeutic areas, including Psychiatry, Acute Post‑Op Pain, Asian Bridging, Dermatology, Gastroenterology, and Neurology. Many of our locations offer in‑patient capabilities and have extensive experience managing complex early‑phase studies.
We prioritize a collaborative and supportive work environment with an emphasis on quality, teamwork, and professional development.
Benefits Full‑time employees are eligible for a competitive compensation package and comprehensive benefits after 30 days of employment, including:
Long‑Term & Short‑Term Disability
Life Insurance
401(k)
Positive workplace culture that emphasizes work‑life balance and strong leadership
Required Skills & Qualifications
Interest in and knowledge of clinical research or specific study indications
Excellent computer skills and proficiency with email, electronic systems, and office equipment
Strong organizational skills and attention to detail
Ability to maintain effective working relationships with supervisors and colleagues
Strong personal initiative and ability to work independently
Ability to stay calm and effective in emergency or high‑pressure situations
Ability to interpret, adapt, and apply guidelines and procedures
Strong verbal and written communication skills
#J-18808-Ljbffr