Clinical Research Coordinator I Exempt

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:

Coordinates or performs biospecimen collection and maintains HIPAA-protected databases connecting patient information to biospecimens used in research. Serves as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners. Collaborates with clinical research supervisors and staff to implement standard operating procedures for the Institute’s research division. Ensures all patient-facing activities comply with clinical research standards and AHRI procedures. Provides concierge-level service for all patient-facing interactions during clinical trials and research studies. Performs patient chart review and data collection. Collaborates with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices to ensure regulatory and protocol compliance. Ensures compliant data entry and data mining into registries, patient records, and research-specific database systems through collaboration with assistant clinical coordinators. Assists Principal Investigators and research staff in developing compliant research protocols and control documents. Maintains sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources. Works flexible hours and is available for research project-related questions. Other duties as assigned Manages all aspects of research including patient screening, eligibility assessment, and follow-up care for volunteers in studies, trials, and programs. Executes and coordinates the informed consent process for research participants in clinical trials and studies across multiple locations.

Knowledge, Skills, and Abilities:

• Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner.

• Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research.

• Ability to communicate effectively with research participants, investigators, research staff, and external partners.

• Ability to apply an analytical approach to problem solving, obtain and analyze facts, and apply sound judgement.

• Ability to accept direction and respond to the changing needs of clinical research units.

• Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skills.

• Proficient in the ability to navigate through various electronic data transfer portals and systems.

• Excellent organizational, multi-tasking, and problem-solving skills with extreme attention to detail.

• Strong interpersonal skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public.

• Excellent understanding of project management concepts in order to ensure protocol compliance.

• Specialized knowledge of the unique needs of patients in the assigned therapeutic areas undergoing treatment.

• Specialized knowledge of assigned therapeutic areas as it relates to research and clinical trials.

• One to two years skill in human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology.

• Bilingual (English/Spanish).

• Clinical Trials Management System (or equivalent) and/or Electronic Data Capture (EDC) exposure.

• Advanced computer skills.

• Knowledge of clinical research and research regulatory environment.

Education:
• Bachelor's [Required]

Work Experience:
• 2+ years of direct clinical research experience [Preferred]

• Healthcare experience (medical assistant, allied health care professional, etc.) within an office or hospital setting. [Preferred]

Additional Information:

An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement:

• Bachelor’s degree in healthcare or related field with no research experience OR

• Bachelor’s degree in any field with research experience OR

• Associate’s degree in healthcare or related field and two (2) years of clinical research or healthcare experience OR

• Graduate of an accredited allied health certificate program with four (4) years of clinical research or healthcare experience

• Other certification as applicable to clinical degree or program (i.e., medical assistant, medical technician, phlebotomy) [Preferred]

Licenses and Certifications:

• Certified Clinical Research Coordinator (CCRC) [Preferred] OR

• Certified Clinical Research Professional (SOCRA) (CCRP) [Preferred] AND

• Basic Life Support – CPR Cert (BLS) [Preferred]

Physical Requirements: (Please click the link below to view work requirements)
Physical Requirements – https://tinyurl.com/23km2677

Pay Range:

$50,835.71 – $94,545.54

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