Job Description

Clinical Research Coordinator - Centennial, CO

Compensation: $50,000 - $70,000 Annually

Overview: Nexus HR is seeking a Clinical Research Coordinator to join our team. In this pivotal role, you will maintain a neat and professional appearance, demonstrate commitment to serve at all times, uphold guidelines as set forth in the employee handbook, and maintain patient confidentiality at all times.

About the Job

The Clinical Research Coordinator is involved in all aspects of clinical trials research from pre-study planning to study completion, and includes direct involvement in case management of study participants. Works under the supervision of the Principal Investigator and Site Manager.

Duties and Responsibilities:

• Own end-to-end management and execution of all clinical research activities

• Independently conduct and complete study visits, including protocol review with the Principal Investigator

• Lead patient recruitment and retention initiatives and support internal study marketing efforts

• Ensure compliant informed consent before any study procedures

• Review medical records and eligibility criteria with investigators or site leadership

• Perform safety assessments (e.g., vitals, venipuncture, ECGs)

• Create, maintain, and complete source documentation and regulatory binders

• Schedule subjects, manage follow-up, and coordinate with physicians and sponsors

• Collaborate with clinical teams to ensure protocol adherence and documentation accuracy

• Complete CRFs and manage queries in a timely, compliant mannerCoordinate research operations across multiple studies, phases, and therapeutic areas

• Complete and maintain training in ICH/GCP, HIPAA, SOPs, IATA, and other required technical skills

• Understand Investigator and Site responsibilities under FDA, DHHS, and OHRP regulations

• Knowledgeable of the drug development process (IND to NDA, IDE to PMA, Phases I–IV)

• Comprehend and communicate informed consent elements per the Declaration of Helsinki

• Understand IRB regulations and their role in clinical trials

• Identify and report adverse and serious adverse events promptly

• Participate in site initiation, monitoring, and closeout visits, as well as sponsor meetings

• Engage in peer review of data quality

• Adhere to IMMUNOe policies and procedures

• Maintain regular attendance as an essential job function

Qualifications :

• Bachelor’s degree in biology, chemistry, human sciences, or a related scientific field; relevant clinical experience may substitute

• 2–5 years of healthcare and/or clinical research experienceCertification in the field (CCRC, CCRA, or CCRP) preferred

• Strong attention to detail and organizational skills

• Excellent written and verbal communication

• Ability to manage multiple studies concurrently

• Proficient in basic computer applications

• Demonstrates honesty, integrity, and professionalism

• Effective team player in a high-performance environment

Benefits:

• 401(k) and 401(k) matching

• Health, dental, and vision insurance

• Life and disability insurance (short-term and long-term)

• Flexible spending accounts (FSA)

• Health Savings Accounts (HSA)

• Employee Assistance Program (EAP)

• Paid time off (PTO) and holiday pay

• Wellness programs

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