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AdventHealth ColoradoPosted 21 days ago

Clinical Research Coorindator II

Full-time
On-site
2+ years
$50K – $93K/yr
Posted 21 days ago

AdventHealth is hiring a Clinical Research Coordinator II to manage and coordinate clinical trial protocols from start-up through completion. The role supports participant consent and advocacy, regulatory compliance, study documentation, and coordination among investigators, research staff, sponsors, and oversight organizations.

Hospital & Health Care

Posted
21 days ago
Source
adventhealth.wd12.myworkdayjobs.com
Sector
Human Resource/Administrative/Legal

Opens the employer's application page in a new tab

Responsibilities

  • Manages multiple clinical trial protocols, coordinates execution and follow-up, and performs accurate documentation
  • Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity issues
  • Simultaneously executes and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties
  • Other duties as assigned
  • Reviews informed consent documents with study candidates and ensures patient advocacy and informed consent throughout the trial
  • Coordinates support staff, laboratory technicians, and assistants to ensure efficient and high-quality results
  • Serves as a liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs
  • Prepares and reviews documentation for clinical research study start-up, execution, modification, renewal, and termination
  • Maintains current knowledge of regulatory requirements and implements changes as needed
  • Collaborates with study sponsors and assists site monitors during visits
  • Works flexible hours and is available for research project-related questions
  • Communicates effectively with healthcare team members, patients, investigators, sponsors, and administration
  • Manages records, study medication, and test articles confidentially and securely

Qualifications

  • Ability to work independently in a fast-paced clinical or research environment
  • Interpersonal communication skills; ability to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances
  • Detail-oriented with teamwork skills; motivated, organized, and capable of performing multiple tasks in a timely manner, and working efficiently under pressure
  • Ability to simultaneously execute and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties
  • Specialized knowledge of the unique needs of patients undergoing treatment in research trials including device management trials
  • Critical thinker with an analytical approach to problem-solving
  • Minimum of two to five years leveraging knowledge of human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology
  • Minimum two to five years understanding and leveraging standard clinical practices with regard to informed consent, biospecimen collection, and handling
  • Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skill
  • Demonstrated proficiency in clinical study coordination across a spectrum of trial acuities
  • Knowledge of Federal regulations: Food and Drug Administration (FDA), Centers for Disease Control (CDC), Department of Health and Human Services (DHHS)
  • Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines
  • An equivalent combination of education ad relevant work experience may be considered in lieu of the stated degree requirement:
  • Bachelors degree and 2+ years of experience OR
  • Associates degree and 4+ years of experience OR
  • Technical/Vocational School and 6+ years of clinical research experience

Preferred

  • Bilingual (English/Spanish)
  • Cardiology experience
  • Certified Clinical Research Coordinator (CCRC)
  • Basic Life Support - CPR Cert (BLS)
  • Advanced Cardiac Life Support Cert (ACLS)

Required skills

Biospecimen Collection and HandlingCDC RegulationsCardiologyClinical ResearchClinical Trial CoordinationDHHS RegulationsFDA RegulationsHuman Life SciencesICH-GCP GuidelinesInformed ConsentOHRP Guidelines

Nice to have

Bilingual (English/Spanish)

Full job description

AdventHealth is hiring a Clinical Research Coordinator II to manage and coordinate clinical trial protocols from start-up through completion. The role supports participant consent and advocacy, regulatory compliance, study documentation, and coordination among investigators, research staff, sponsors, and oversight organizations.

Hospital & Health Care

  • Insider Connection @AdventHealth Colorado
  • 2 email credits available today
  • Beyond your network
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  • Associate HR Business Partner
  • From your previous company
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Responsibilities

  • Manages multiple clinical trial protocols, coordinates execution and follow-up, and performs accurate documentation
  • Promotes Principal Investigator oversight by advising on deviations, patient status, and trial integrity issues
  • Simultaneously executes and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties
  • Other duties as assigned
  • Reviews informed consent documents with study candidates and ensures patient advocacy and informed consent throughout the trial
  • Coordinates support staff, laboratory technicians, and assistants to ensure efficient and high-quality results
  • Serves as a liaison between Principal Investigators, the Institutional Review Board, and the Office of Sponsored Programs
  • Prepares and reviews documentation for clinical research study start-up, execution, modification, renewal, and termination
  • Maintains current knowledge of regulatory requirements and implements changes as needed
  • Collaborates with study sponsors and assists site monitors during visits
  • Works flexible hours and is available for research project-related questions
  • Communicates effectively with healthcare team members, patients, investigators, sponsors, and administration
  • Manages records, study medication, and test articles confidentially and securely

Preferred

  • Bilingual (English/Spanish)
  • Cardiology experience
  • Certified Clinical Research Coordinator (CCRC)
  • Basic Life Support - CPR Cert (BLS)
  • Advanced Cardiac Life Support Cert (ACLS)

Benefits

  • 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
  • At AdventHealth, Extending the Healing Ministry of Christ is our mission. It calls us to be His hands and feet in helping people feel whole.
  • Denver, US
  • https://networkofcare.adventhealth.com/colorado
  • Distribution of Different Job Fields Receiving Sponsorship
  • Represents job field similar to this job
  • Engineering and Development
  • Customer Service and Support
  • Trends of Total Sponsorships
  • *2026
  • (3)
  • 2025
  • (1)
  • 2023
  • (6)
  • 2022
  • (2)
  • Late Stage
  • Leadership Team
  • Brett Spenst
  • Chief Executive Officer
  • Matt Gal

Qualifications

  • Ability to work independently in a fast-paced clinical or research environment
  • Interpersonal communication skills; ability to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances
  • Detail-oriented with teamwork skills; motivated, organized, and capable of performing multiple tasks in a timely manner, and working efficiently under pressure
  • Ability to simultaneously execute and coordinate multiple clinical trials and function independently; perform diverse clinical and clerical duties
  • Specialized knowledge of the unique needs of patients undergoing treatment in research trials including device management trials
  • Critical thinker with an analytical approach to problem-solving
  • Minimum of two to five years leveraging knowledge of human life sciences/biomedical research; physiological, cellular, biochemical, or molecular biology
  • Minimum two to five years understanding and leveraging standard clinical practices with regard to informed consent, biospecimen collection, and handling
  • Working knowledge of Microsoft Office applications, such as Word, Excel, Access, Outlook, and Internet knowledge and skill
  • Demonstrated proficiency in clinical study coordination across a spectrum of trial acuities
  • Knowledge of Federal regulations: Food and Drug Administration (FDA), Centers for Disease Control (CDC), Department of Health and Human Services (DHHS)
  • Bachelor's
  • 2+ clinical research
  • Research experience including awareness of FDA / OHRP / ICH / GCP Guidelines and relevant state and federal regulatory/statutory guidelines
  • An equivalent combination of education ad relevant work experience may be considered in lieu of the stated degree requirement:
  • Bachelors degree and 2+ years of experience OR
  • Associates degree and 4+ years of experience OR
  • Technical/Vocational School and 6+ years of clinical research experience
  • Bilingual (English/Spanish)
  • Cardiology experience
  • Certified Clinical Research Coordinator (CCRC)
  • Basic Life Support - CPR Cert (BLS)
  • Advanced Cardiac Life Support Cert (ACLS)
  • Technical/Vocational School and 6+ years of clinical research experience.

Required skills

  • Biospecimen Collection and Handling, CDC Regulations, Cardiology, Clinical Research, Clinical Trial Coordination, DHHS Regulations, FDA Regulations, Human Life Sciences, ICH-GCP Guidelines, Informed Consent, OHRP Guidelines

Preferred skills

  • Advanced Cardiac Life Support Cert (ACLS), Basic Life Support - CPR Cert (BLS), Bilingual (English/Spanish), Cardiology experience, Certified Clinical Research Coordinator (CCRC)

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 23, 2026

Work mode

On-site

Job source

adventhealth.wd12.myworkdayjobs.com

Company

AdventHealth Colorado

Human Resource/Administrative/Legal

See all 5 jobs from AdventHealth Colorado →
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