What are the responsibilities and job description for the Clinical Research Coordinator II position at AdventHealth Central Florida?
Clinical Research Coordinator II AdventHealth Orlando
All the benefits and perks you need for you and your family :
- Benefits from Day One
- Paid Days Off from Day One
- Student Loan Repayment Program
- Career Development
- Whole Person Wellbeing Resources
- Mental Health Resources and Support
- Pet Insurance
- Debt-free Education
- Certifications and Degrees without out-of-pocket tuition expense)
- Nursing Clinical Ladder Program
- Sign-on Bonus
- Relocation Bonus
- Team Based Nursing Model _
- Nursing or BU specific benefits and perks
Our promise to you :
Joining AdventHealth is about being part of something bigger. Its 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.
Schedule : Full Time, Days
Shift : 8 : 00 am to 4 : 30 pm
Location : 265 E. Rollins Street, Suite 2000, Orlando, FL 32804
The community youll be caring for : AdventHealth Orlando
The role youll contribute :
The Clinical Research Coordinator II (CRC II) serves the AdventHealth Research Institute (AHRI), under limited supervision, to plan, coordinate, evaluate and perform the nursing care of participants and collect data for assigned research projects. The CRC II follows study specific protocol guidelines, communicates with AHRI Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead and clinical research support staff. The CRC II works to advocate for the patient, while adhering to the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, Food and Drug Administration (FDA) regulations and International Conference on Harmonization / Good Clinical Practices (ICH / GCP) guidelines.
The value youll bring to the team :
Utilizes positive interpersonal communication skills; communicates effectively with members of the healthcare team, patients, investigators, sponsors of research and administration.
Reviews all elements of the current institutional IRB approved informed consent (IC) document, according to current FDA, state, federal and institutional regulations with study candidates and / or legal representative; ensures, through patient advocacy and informed consent as an ongoing process, that the rights, safety and well-being of trial subjects are the most important considerations and should prevail over the interests of science and society.
Manages multiple clinical trial protocols, coordinates the execution and follow-up of each protocol, seeks and utilizes resources and works independently; performs accurate, legible and timely documentation. Manages records, study medication and test articles in confidential and secure manner.
Promotes Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Supervisor and / or Clinical Operations Manager of deviations in conduct, patient status, issues relevant to the integrity of the trial and / or the safety of research subjects; abides by hospital and departmental policies and SOPs, as well as all applicable local, state, and federal regulations.
Coordinates the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols.
Serves as liaison between Principal Investigators and the Institutional Review Board (IRB) and the Office of Sponsored Programs (OSP). Prepares and / or reviews all required documentation for clinical research study start up, execution, modification, renewal, and termination and will meet all reasonable deadlines for submission. Maintains timely turnaround of all documents to avoid delays in study initiation and / or progress. Remains current on rapidly changing regulatory requirements and HIPAA regulations and implements these changes as appropriate and in a timely manner.
Collaborates with study sponsors. Assists site monitors during their visits in a professional manner.
Works flexible hours and is available as a resource for questions related to research projects.
Performs other duties as assigned or directed to ensure smooth and efficient operations of the FHRI and Core. Communicates the need for new work and automatically looks for additional duties as workload permits.
The expertise and experiences youll need to succeed :
Preferred qualifications :
o Masters degree in Healthcare, Research or related field
o Experience in area of specialty, as assigned
o Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA)
o American Heart Association Basic Life Support (BLS)
o American Heart Association Advanced Cardiovascular Life Support (ACLS)
o Other certification as applicable to degree or program (i.e. medical assistant, medical technician, phlebotomy)
o 2 / 28 / 22
This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location.
Category : Research
Organization : AdventHealth Orlando
Schedule : Full-time
Shift : 1 - Day
Req ID : 24045513
We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability / handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.
