Urology Clinical Research Coordinator-RN

1106 Portercare Adventist Health System; United States; On-site; USD 72,000 - 124,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401-K Retirement Plan

Paid Time Off from Day One

Parental Leave

Career Development

Mental Health Resources

Pet Benefits

Job summary

AdventHealth seeks a Clinical Research Coordinator to manage informed consent, screen participants, and explain study details to volunteers. You will maintain study records, coordinate biospecimen collection, and serve as a point of contact for participants, investigators, and staff.

The role requires RN licensure, strong organizational skills, and the ability to work in a fast-paced clinical research setting. Oncology or related trials experience is a plus.

Qualifications

• RN with active license in good standing.
• Experience coordinating clinical trials preferred.
• Bilingual English/Spanish preferred.
• Familiar with HIPAA and research participant privacy.

Responsibilities

• 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 information about the study, including purpose, procedures, risks, and benefits, to potential participants.
• Maintains accurate records of the informed consent process and signed forms.
• Coordinates biospecimen collection and maintains HIPAA-protected databases linking patient info to biospecimens.

Skills

Clinical tasks

Independent work

Phlebotomy

IV insertion

HIPAA knowledge

Communication

Analytical thinking

Microsoft Office

Bilingual

Education

Associate's Degree in Nursing

Bachelor's Degree in Nursing

Tools

Microsoft Office

Job description

Benefits and Perks

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

Location and Schedule

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
• [Preferred] 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)

Education

• Associate's of Nursing [Required]
• Bachelor's of Nursing [Preferred]
• Field of Study: Nursing

Work Experience

Work Experience: N/A

Additional Information

Additional Information: N/A

Licenses and Certifications

• Registered Nurse (RN) [Required]
• Basic Life Support - CPR Cert (BLS) [Required]
• Certified Clinical Research Coordinator (CCRC) [Preferred]

Physical Requirements

Physical Requirements: (Please click the link below to view work requirements) Physical Requirements - https://tinyurl.com/msy4mja2

Pay Range

Pay Range: $71,968.00 - $124,446.40

Equal Opportunity Employer

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances.

Mission

Every day, our fellow team members show up to work, unified by one shared mission: Extending the Healing Ministry of Jesus Christ. As a faith-based health care organization, our story is one of hope as we strive to heal and restore the body, mind and spirit. Though our facilities are spread across the country, this unwavering belief binds us together. Across every office, exam and patient room, we’re committed to providing individualized, holistic care. This is our Christian mission, and it inspires us to help make communities healthier and happier.