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