Job Description

Clinical Research Coordinator – Direct Hire (On-Site)

Schedule: Monday – Friday, 8:00 AM – 5:00 PM

Location: Englewood, Colorado

Employment Type: Full-Time | Direct Hire

About the Role

We are seeking an experienced and detail-oriented Clinical Research Coordinator to join our clinical research team in Englewood, CO. This position is responsible for coordinating all aspects of clinical trials with strict adherence to ICH, GCP, study protocols, and company policies. The ideal candidate is proactive, organized, and passionate about advancing clinical research excellence from study start-up through completion.

Key Responsibilities

• Coordinate all aspects of patient participation from study initiation through completion.
• Assist with study start-up activities, including preparation of accurate source documents and collaboration with sponsors, investigators, and internal departments.
• Participate in investigator meetings (IMs) and site initiation visits (SIVs).
• Screen and consent participants, ensuring eligibility and understanding of study protocols.
• Educate participants and caregivers on study expectations and procedures.
• Conduct and/or coordinate study-related assessments (vital signs, ECGs, blood draws, etc.).
• Maintain accurate and timely source documentation and data entry.
• Report serious adverse events (SAEs), protocol deviations, and other reportable items promptly.
• Coordinate with research pharmacists on drug accountability and compliance.
• Prepare for and facilitate monitoring visits; respond promptly to follow-up communications.
• Maintain professional and effective communication with sponsors, CROs, investigators, and site staff.
• Ensure ongoing compliance with all regulatory and protocol requirements.

Required Qualifications

• Bachelor’s degree or equivalent experience in Clinical Research or a related field.
• Proven experience as a Clinical Research Coordinator
• In-depth understanding of Federal regulations, ICH-GCP, and human subject protection.
• Strong leadership, problem-solving, and communication skills.
• High attention to detail, accuracy, and ability to manage multiple priorities.
• Proficiency with study-related technology and data entry systems.
• Ability to work independently and collaboratively within a multidisciplinary team.

Preferred Qualifications

• Experience training or mentoring junior research staff.
• Demonstrated crisis management and critical thinking skills.
• Familiarity with medical terminology and use of medical instruments for subject assessments.

What We Offer

• Competitive compensation package.
• Comprehensive benefits after 30 days of employment, including:
• Health, Dental, and Vision Insurance
• Life, LTD, and STD Insurance
• 401(k) with company match
• Supportive, team-oriented environment focused on quality, collaboration, and professional growth.

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