Clinical Research Coordinator I - Intermountain Health
Murray, UT
About the Job
Job Description:
This position assists in managing clinical research studies for Transplant Research and is responsible for the efficient coordination of clinical studies by working closely with clinical investigators, study sponsors, department managers, other caregiver, and the patients who participate in research studies.
A Clinical Research Coordinator (CRC) supports multiple clinical research studies ensuring adherence to federal/local/institutional regulatory requirements, good clinical practice, data quality, protocol compliance, protection of human subjects, and overall quality assurance and quality management.
In this role, you will contribute to the overall clinical research/trial/study activities from design, set up, conduct, through closeout. You will be responsible for the implementation of research activities for one or more studies. As our Research Coordinator, you will recognize and perform necessary tasks to manage projects and prioritize work to meet necessary deadlines. You will be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). Along with clinical investigators, you will be the primary point of contact for patients who participate in research
Job Essentials
+ Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
+ Determine eligibility of and gather consent from study participants according to protocol. Assist with recruitment strategies.
+ Coordinate collection of study specimens and processing.
+ Collect and manage study participants, imaging, study drug accountability, and laboratory data for research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
+ Ensure compliance with research protocols, and review case report forms for completion and accuracy with source documents.
+ Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend regular meetings with staff/principal investigator, acting as primary contact.
+ Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
+ Ensure essential documentation and recording of participant and research data in appropriate files per institutional and regulatory requirements.
+ Participate in monitoring visits and regulatory audits.
+ Work closely with internal departments such as radiology, pharmacy, and laboratory to schedule research activities for patients
+ Collaboration with team members
+ _-Other duties may also be assigned_
Minimum Qualifications
+ Three years of clinical research experience worked with human subjects.
OR
+ BA degree and 1 year if clinical research experience working with human subjects.
OR
+ Professional certifications such as the CCRP (Certified Clinical Research Professional- SoCRA), CCRC (Certified Clinical Research Coordinator - ACRP), CIRB Certified Institutional Review Board professional or CRA Certified Research Administrator - which require 2 years of research experience and a test.
+ BA degree and 1 year if clinical research experience working with human subjects.
+ Experience using basic computer programs including word processing, database, spreadsheet applications and e-mail.
+ Experience using laboratory protocol, systems and documentation techniques.
Preferred Qualifications
+ Bachelor's Degree or higher from an accredited institution.
+ Prior experience in healthcare setting working directly with patients
+ Expertise or prior experience in Hepatology, Gastroenterology, Abdominal Transplant
+ Prior experience with electronic medical records systems
+ Prior experience with Microsoft Office applications
+ Strong interpersonal skills
+ Knowledge of medical terminology
Physical Requirements:
Interact with others by effectively communicating, both orally and in writing.
- and -
Operate computers and other office equipment requiring the ability to move fingers and hands.
- and -
See and read computer monitors and documents.
- and -
Remain sitting or standing for long periods of time to perform work on a computer, telephone, or other equipment.
- and -
May require lifting and transporting objects and office supplies, bending, kneeling and reaching.
Location:
Intermountain Medical Center
Work City:
Murray
Work State:
Utah
Scheduled Weekly Hours:
40
The hourly range for this position is listed below. Actual hourly rate dependent upon experience.
$24.29 - $38.26
We care about your well-being – mind, body, and spirit – which is why we provide our caregivers a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged.
Learn more about our comprehensive benefits packages for our Idaho, Nevada, and Utah based caregivers (https://intermountainhealthcare.org/careers/working-for-intermountain/employee-benefits/) , and for our Colorado, Montana, and Kansas based caregivers (http://www.sclhealthbenefits.org) ; and our commitment to diversity, equity, and inclusion (https://intermountainhealthcare.org/careers/working-for-intermountain/diversity/) .
Intermountain Health is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
All positions subject to close without notice.
This position assists in managing clinical research studies for Transplant Research and is responsible for the efficient coordination of clinical studies by working closely with clinical investigators, study sponsors, department managers, other caregiver, and the patients who participate in research studies.
A Clinical Research Coordinator (CRC) supports multiple clinical research studies ensuring adherence to federal/local/institutional regulatory requirements, good clinical practice, data quality, protocol compliance, protection of human subjects, and overall quality assurance and quality management.
In this role, you will contribute to the overall clinical research/trial/study activities from design, set up, conduct, through closeout. You will be responsible for the implementation of research activities for one or more studies. As our Research Coordinator, you will recognize and perform necessary tasks to manage projects and prioritize work to meet necessary deadlines. You will be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). Along with clinical investigators, you will be the primary point of contact for patients who participate in research
Job Essentials
+ Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
+ Determine eligibility of and gather consent from study participants according to protocol. Assist with recruitment strategies.
+ Coordinate collection of study specimens and processing.
+ Collect and manage study participants, imaging, study drug accountability, and laboratory data for research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
+ Ensure compliance with research protocols, and review case report forms for completion and accuracy with source documents.
+ Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend regular meetings with staff/principal investigator, acting as primary contact.
+ Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
+ Ensure essential documentation and recording of participant and research data in appropriate files per institutional and regulatory requirements.
+ Participate in monitoring visits and regulatory audits.
+ Work closely with internal departments such as radiology, pharmacy, and laboratory to schedule research activities for patients
+ Collaboration with team members
+ _-Other duties may also be assigned_
Minimum Qualifications
+ Three years of clinical research experience worked with human subjects.
OR
+ BA degree and 1 year if clinical research experience working with human subjects.
OR
+ Professional certifications such as the CCRP (Certified Clinical Research Professional- SoCRA), CCRC (Certified Clinical Research Coordinator - ACRP), CIRB Certified Institutional Review Board professional or CRA Certified Research Administrator - which require 2 years of research experience and a test.
+ BA degree and 1 year if clinical research experience working with human subjects.
+ Experience using basic computer programs including word processing, database, spreadsheet applications and e-mail.
+ Experience using laboratory protocol, systems and documentation techniques.
Preferred Qualifications
+ Bachelor's Degree or higher from an accredited institution.
+ Prior experience in healthcare setting working directly with patients
+ Expertise or prior experience in Hepatology, Gastroenterology, Abdominal Transplant
+ Prior experience with electronic medical records systems
+ Prior experience with Microsoft Office applications
+ Strong interpersonal skills
+ Knowledge of medical terminology
Physical Requirements:
Interact with others by effectively communicating, both orally and in writing.
- and -
Operate computers and other office equipment requiring the ability to move fingers and hands.
- and -
See and read computer monitors and documents.
- and -
Remain sitting or standing for long periods of time to perform work on a computer, telephone, or other equipment.
- and -
May require lifting and transporting objects and office supplies, bending, kneeling and reaching.
Location:
Intermountain Medical Center
Work City:
Murray
Work State:
Utah
Scheduled Weekly Hours:
40
The hourly range for this position is listed below. Actual hourly rate dependent upon experience.
$24.29 - $38.26
We care about your well-being – mind, body, and spirit – which is why we provide our caregivers a generous benefits package that covers a wide range of programs to foster a sustainable culture of wellness that encompasses living healthy, happy, secure, connected, and engaged.
Learn more about our comprehensive benefits packages for our Idaho, Nevada, and Utah based caregivers (https://intermountainhealthcare.org/careers/working-for-intermountain/employee-benefits/) , and for our Colorado, Montana, and Kansas based caregivers (http://www.sclhealthbenefits.org) ; and our commitment to diversity, equity, and inclusion (https://intermountainhealthcare.org/careers/working-for-intermountain/diversity/) .
Intermountain Health is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
All positions subject to close without notice.
Source : Intermountain Health