Clinical Research Coordinator – Denver, CO Clinical Research Site Network

Green Life Science; Denver (CO); Híbrido; USD 65 000 - 90 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive salary

Professional development opportunities

Long-term career growth

Resumo da oferta

Green Life Science is seeking a Clinical Research Coordinator in Denver, Colorado to join a fast-paced, patient-facing research environment. You will coordinate studies from start-up through close-out across a diverse portfolio, ensuring data quality, patient care and regulatory compliance.

The ideal candidate will have hands-on experience with GCP, FDA regulations, vital signs, ECGs, phlebotomy and source documentation, plus strong communication and attention to detail to support recruitment

Qualificações

• Minimum experience as a CRC in a clinical research site.
• Strong knowledge of GCP and FDA regulations.
• Experience supporting patient recruitment and retention.

Responsabilidades

• Coordinate clinical research studies in accordance with protocols, GCP and applicable regulations.
• Conduct patient-facing study visits including screening, enrollment, follow-up and end-of-study visits.
• Support patient recruitment, prescreening, scheduling and retention activities.
• Perform and document clinical procedures including: vital signs, 12-lead ECGs, phlebotomy and specimen processing.
• Maintain accurate source documentation and study records; complete EDC entries and respond to data queries.

Conhecimentos

GCP knowledge

Clinical trial coordination

Communication

Attention to detail

Independent work

Formação académica

Bachelor's degree in life sciences

Ferramentas

EDC systems

Descrição da oferta de emprego

Clinical Research Coordinator – Denver, CO

Location: Denver, Colorado, United States

About The Role

A rapidly growing clinical research site network is seeking an experienced Clinical Research Coordinator (CRC) to join its Denver, Colorado team.

This is an excellent opportunity for a hands‑on CRC who enjoys a fast-paced, patient-facing research environment and wants to work across a diverse portfolio of clinical trials.

The ideal candidate will have strong experience coordinating clinical trials from start-up through close-out, with a genuine focus on patient care, recruitment, data quality and study execution

Key Responsibilities

• Coordinate clinical research studies in accordance with protocols, GCP and applicable regulations.
• Conduct patient-facing study visits, including screening, enrollment, follow-up and end-of-study visits.
• Support patient recruitment, prescreening, scheduling and retention activities.
• Perform and document clinical procedures including:
• Vital signs
• 12-lead ECGs
• Phlebotomy / blood draws
• Specimen processing and shipment
• Medication administration, where applicable
• Collection of medical history and source documentation
• Maintain accurate and complete source documentation and study records.
• Complete EDC entries and respond to data queries within required timelines.
• Coordinate with Principal Investigators, Sub-Investigators, sponsors, CROs and other study stakeholders.
• Ensure study activities remain compliant with GCP, FDA regulations, protocols and SOPs.
• Support monitoring visits, audits and inspection readiness.
• Manage study supplies, investigational product accountability and laboratory requirements where applicable.
• Identify and **escalate** protocol deviations, safety concerns and operational issues.
• Maintain strong communication with study participants throughout the clinical trial journey.#

Ideal Background

• Previous experience as a Clinical Research Coordinator within a clinical research site.
• Experience working directly with study participants in a busy research environment.
• Strong knowledge of GCP and clinical trial processes.
• Hands‑on experience with vital signs, ECGs and phlebotomy strongly preferred.
• Experience supporting patient recruitment and retention.
• Ability to manage multiple protocols and priorities simultaneously.
• Strong attention to detail and accurate documentation skills.
• Excellent communication and interpersonal skills.
• Comfortable working independently while contributing to a collaborative site team.
• Experience across Phase I–IV clinical trials is highly desirable.
• Exposure to areas such as metabolic, cardiology, CNS, respiratory, infectious disease or vaccine research would be advantageous.

What’s on Offer

• Opportunity to join a high-growth clinical research organisation.
• Exposure to a diverse and expanding clinical trial portfolio.
• Hands‑on, patient-facing research environment.
• Strong opportunities for professional development and progression.
• Collaborative and supportive clinical research team.
• Competitive salary and benefits package.
• Opportunity to build a long‑term career within a growing research network.