Clinical Research Coordinator II Non-RN Oncology

4 weeks ago

Orlando, United States AdventHealth Full time

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

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.

Schedule: Full Time

Shift : Monday - Friday, Days

Location : AdventHealth East Orlando

The role you'll 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.

Works closely with AHRI Core managers to schedule clinical operations to facilitate the initiation and completion of clinical research studies, the CRC II also promotes Principal Investigator (PI) oversight by advising the PI, sub-investigator(s), Lead and Director of deviations in conduct, patient status, issues relevant to the integrity of the trial and/or the safety of research subjects. Actively participates in outstanding customer service and accepts responsibility in maintaining relationships that are equally respectful to all.

The value you'll 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.

Qualifications

The expertise and experiences you'll need to succeed:

  • 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 and has teamwork skills; motivated, organized, ability to perform multiple tasks in a timely manner, and work efficiently under pressure

  • Simultaneously executes 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

  • Ability to be a 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 of 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

  • Bachelor's Degree and 2 years of experience in clinical research or

  • Associates degree and 4 years of experience in clinical research or related field or

  • Graduate of an accredited allied health certificate program with six (6) years of clinical research or healthcare experience.

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: 24026396

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.

  • Clinical Research Coordinator

    2 weeks ago

    Orlando, United States Actalent Full time

    Job Title: Clinical Research Coordinator Job Description The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects. The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI),...

  • Clinical Research Coordinator

    3 weeks ago

    Orlando, Florida, United States Actalent Full time

    Job Title: Clinical Research CoordinatorJob Description The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects. The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI),...

  • Clinical Research Coordinator

    3 weeks ago

    Orlando, United States Actalent Full time

    Job Title: Clinical Research Coordinator Job Description The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects. The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI),...

  • Clinical Research Coordinator

    1 month ago

    Orlando, United States Charter Research Full time

    Clinical Research CoordinatorCOMPANY DESCRIPTIONCharter Research is a highly experienced and quickly growing clinical research company, based in The Villages and Orlando, FL that is looking to add to our team to help us fulfill our mission of discovering future medicines. Our company is locally owned and prides itself on providing exceptional patient...

  • Clinical Research Coordinator

    2 months ago

    Orlando, United States Charter Research Full time

    Clinical Research CoordinatorCOMPANY DESCRIPTIONCharter Research is a highly experienced and quickly growing clinical research company, based in The Villages and Orlando, FL that is looking to add to our team to help us fulfill our mission of discovering future medicines. Our company is locally owned and prides itself on providing exceptional patient...

  • Clinical Research Supervisor Oncology RN

    2 hours ago

    Orlando, Florida, United States AdventHealth Full time

    About the RoleWe are seeking a highly skilled Clinical Research Supervisor Oncology RN to join our team at AdventHealth. As a key member of our research operations team, you will be responsible for overseeing the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP...

  • Clinical Research Coordinator

    2 months ago

    Orlando, United States CHARTER RESEARCH Full time

    Job DescriptionJob DescriptionCOMPANY DESCRIPTIONCharter Research is a highly experienced and quickly growing clinical research company, based in The Villages and Orlando, FL that is looking to add to our team to help us fulfill our mission of discovering future medicines. Our company is locally owned and prides itself on providing exceptional patient...

  • Clinical Research Nurse

    3 weeks ago

    Orlando, United States Actalent Full time

    Job Title: Clinical Research Coordinator Job Description The Clinical Research Coordinator, under limited supervision, plans, coordinates, evaluates, and performs the care of participants and collects data for assigned research projects. The CRC-II (Non-RN) follows study-specific protocol guidelines, communicates with Principal Investigators (PI),...

  • Clinical Research Coordinator

    3 weeks ago

    Orlando, Florida, United States Actalent Full time

    Job Title: Clinical Research Coordinator II*This is a fully on-site position in Orlando, FloridaJob DescriptionThe Clinical Research Coordinator (Non-RN) manages all aspects of research, including patient screening, eligibility assessment, and coordination of care and follow-up for volunteers in research studies, trials, and programs. Key activities include...

  • Clinical Research Coordinator

    2 weeks ago

    Orlando, Florida, United States Actalent Full time

    Job Title: Clinical Research Coordinator II*This is a fully on-site position in Orlando, FloridaJob DescriptionThe Clinical Research Coordinator (Non-RN) manages all aspects of research, including patient screening, eligibility assessment, and coordination of care and follow-up for volunteers in research studies, trials, and programs. Key activities include...

  • Clinical Research Coordinator

    3 weeks ago

    Orlando, United States Actalent Full time

    Job Title: Clinical Research Coordinator II *This is a fully on-site position in Orlando, Florida Job Description The Clinical Research Coordinator (Non-RN) manages all aspects of research, including patient screening, eligibility assessment, and coordination of care and follow-up for volunteers in research studies, trials, and programs. Key...

  • Clinical Research Coordinator

    2 weeks ago

    Orlando, United States Actalent Full time

    Job Title: Clinical Research Coordinator II *This is a fully on-site position in Orlando, Florida Job Description The Clinical Research Coordinator (Non-RN) manages all aspects of research, including patient screening, eligibility assessment, and coordination of care and follow-up for volunteers in research studies, trials, and programs. Key...

  • Clinical Research Coordinator II

    3 months ago

    Orlando, United States DLCFL Full time

    Job DescriptionJob DescriptionThis position is responsible for performing highly diverse clinical and administrative responsibilities requiring a high level of knowledge and attention to detail. This position requires assimilating vast amounts of information and processing information promptly and orderly. Personnel who fill this role must have a working...

  • Clinical Research Nurse II

    4 weeks ago

    Orlando, United States Nemours Full time

    The Clinical Research Nurse II coordinates, implements and completes clinical research studies and/or clinical trials by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study...

  • Clinical Research Nurse

    1 month ago

    Orlando, United States Actalent Full time

    Clinical Research Nurse Must have active Florida RN license and clinical trials experience Job Description: The Clinical Research Coordinator II RN (CRC-II RN) is responsible for planning, coordinating, evaluating, and executing nursing care for participants, as well as collecting data for assigned research projects at the Research Institute. This role...

  • Clinical Research Nurse II

    23 hours ago

    Orlando, United States Nemours Children's Health Full time

    Job DescriptionThe Clinical Research Nurse II coordinates, implements and completes clinical research studies and/or clinical trials by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and...

  • Clinical Research Nurse II

    2 days ago

    Orlando, United States Nemours Children's Health Full time

    Job Description The Clinical Research Nurse II coordinates, implements and completes clinical research studies and/or clinical trials by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and...

  • Clinical Research Coordinator I

    3 weeks ago

    Orlando, Florida, United States AdventHealth Full time

    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 Our promise to you: Joining AdventHealth is about being part of something bigger. It's about belonging to a community...

  • Clinical Research Support Specialist

    3 days ago

    Orlando, Florida, United States CHARTER RESEARCH Full time

    Job OverviewCompany OverviewCharter Research is a dynamic and rapidly expanding clinical research organization dedicated to the advancement of medical science. We focus on delivering exceptional experiences for our participants while implementing effective recruitment strategies for our sponsors. Our team-oriented culture is essential to our mission of...

  • Clinical Research Support Specialist

    3 days ago

    Orlando, Florida, United States CHARTER RESEARCH Full time

    Job OverviewCompany OverviewCharter Research is a dynamic and rapidly expanding clinical research organization dedicated to advancing medical science. We focus on delivering exceptional experiences for our participants while implementing effective recruitment strategies for our sponsors. Our team is built on collaboration, and we are looking for a dedicated...