Oncology Clinical Research Coordinator-RN

AdventHealth

Parker (CO)

On-site

USD 71,260 - 123,215

Full time

14 days+

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Benefits offered by this job

Benefits from Day One: Medical, Dental

401(k) Retirement Plan

Paid Time Off from Day One

Family leave

Career Development

Whole Person Well‑being Resources

Mental Health Resources and Support

Pet Benefits

Job summary

AdventHealth Denver is seeking a Research Coordinator to execute and coordinate informed consent for clinical trials, screen participants, and provide study information while ensuring understanding and HIPAA compliance.

You will maintain records, coordinate biospecimen collection, serve as primary contact, assist with budgets, and support participants throughout studies. Requires RN license, strong clinical competencies, and ability to work in a fast-paced environment.

Qualifications

RN licensing and nursing education are required.
Ability to work in fast-paced clinical or research environments.
Strong communication and data handling skills.
Familiarity with HIPAA and patient advocacy is required.

Responsibilities

Execute and coordinate informed consent for participants in clinical trials.
Screen participants for eligibility and explain study details and risks.
Maintain accurate records of the consent process and study documents.
Coordinate biospecimen collection and connect data to specimens in HIPAA-compliant databases.
Serve as clinical point of contact for participants, investigators and staff.
Assist with budget oversight and resource conservation.
Support participants throughout duration of studies and respond to questions.

Skills

Clinical research coordination

HIPAA knowledge

Communication skills

Microsoft Office

Bilingual English/Spanish

Education

Associate's of Nursing

Bachelor's of Nursing

Tools

Microsoft Office Suite

Job description

Our Promise To You

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by extending the healing ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose‑minded team. All while understanding that together we are even better.

All the benefits and perks you need for you and your family

Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance
Paid Time Off from Day One
403-B Retirement Plan
4 Weeks 100% Paid Parental Leave
Career Development
Whole Person Well‑being Resources
Mental Health Resources and Support
Pet Benefits

Schedule

Full time

Shift

Day (United States of America)

Address

2525 S DOWNING ST

City

DENVER

State

Colorado

Postal Code

80210

Job Description

Executes and coordinates the informed consent process for participants in clinical trials and research studies. Screens potential research participants to determine eligibility for clinical trials and studies. Provides detailed information about the study, including its purpose, procedures, risks, and benefits, to potential participants. Ensures that participants fully understand the informed consent document before they sign it, and clarifies any questions or concerns. Maintains accurate and complete records of the informed consent process, including signed consent forms and documentation of discussions. Coordinates or performs biospecimen collection and maintains HIPAA protected database connecting patient information to biospecimens used in research. Serves as the study‑specific clinical point of contact for participants, investigators, research staff, hospital departments and external research partners. Maintains sensitivity to cost containment measures by conserving hospital supplies and human resources while overseeing proposed project budgets. Conducts research regarding patient screening and clinical eligibility assessments. Coordinates the care and follow‑up of volunteers placed on research studies, trials, and programs. Provides ongoing support and information to participants throughout the duration of studies. Works flexible hours and is available for research project‑related questions. Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice. Ability to work independently in a fast‑paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner. Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. Other duties as assigned.

Knowledge, Skills, and Abilities

Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice. [Required]
Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner [Required]
Ability to acclimate and integrate into various clinical settings as needed per protocol [Required]
Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. [Required]
Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research [Required]
Ability to communicate effectively with research participants, investigators, research staff and external partners. [Required]
Ability to apply analytical approach to problem solving, obtain and analyze facts, and apply sound judgement. [Required]
Ability to accept direction and respond to the changing needs of clinical research units [Required]
Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skill [Required]
Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment [Preferred]
Specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials. [Preferred]
One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology [Preferred]
Bilingual (English/Spanish) [Preferred]