Clinical Research Coord I RN

1103 Team Member Services; United States; In loco; USD 66.000 - 110.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

PTO from Day One

403-B Retirement Plan

Parental Leave

Career Development

Well-being Resources

Mental Health Resources

Pet Benefits

Descrizione del lavoro

AdventHealth in Florida seeks a Research Coordinator to execute and coordinate the informed consent process for participants in clinical trials and research studies, screening for eligibility and informing about study details.

You will maintain records, coordinate biospecimen collection, act as the study contact, and support budgets and multidisciplinary teams while working in a fast-paced clinical research environment.

Competenze

• Active RN license required.
• HIPAA knowledge and patient advocacy required.
• Ability to work independently in a fast-paced clinical/research environment.
• Bilingual English/Spanish preferred.

Mansioni

• Execute and coordinate the informed consent process for participants in clinical trials and research studies.
• Screen potential participants to determine eligibility for trials and studies.
• Provide detailed information about the study, including purpose, procedures, risks and benefits.
• Maintain accurate records of informed consent, including signed forms and discussions.
• Coordinate biospecimen collection and HIPAA-protected data linking patient information to biospecimens.
• Serve as the study-specific clinical point of contact for participants, investigators, staff and partners.
• Support project budgets and conserve resources while overseeing proposed budgets.

Conoscenze

Clinical tasks

Independent work

HIPAA knowledge

Communication

Microsoft Office

Formazione

Associate's Nursing

Bachelor's Nursing

Strumenti

BLS

Descrizione del lavoro

Benefits and Perks

• Benefits from Day One
• Medical Insurance
• Dental Insurance
• 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 and Location

• Full time
• Shift: Day (United States of America)
• Address: 400 CELEBRATION PL
• City: CELEBRATION
• State: Florida
• Postal Code: 34747

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 & 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]

Education

• Associate's of Nursing [Required]
• Bachelor's of Nursing [Preferred]

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

$66,248.00 - $109,740.80

Background Screening Requirement (Florida Law)

Certain positions are subject to Florida Level 2 background screening, including fingerprinting, as required by state law. Applicants may review general information about Florida’s background screening requirements at the Florida Care Provider Background Screening Clearinghouse: https://info.flclearinghouse.com/

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