Clinical Research Specialist, Clinical Learning Environment Job at Community Health System - CA
Community Health System - CA Fresno, CA 93721
$31.20 - $45.86 an hour
Overview:
We are looking for a Clinical Research Specialist to join our growing team! Working closely with the Principal Investigator, you will be responsible for clinical trials, including facilitating and coordinating daily study activities. In your role, you will consistently have the opportunity to lead our research efforts! You should possess the ability to carry out proper handling of highly sensitive information, all the while following protocol and maintaining IRB approval. From study testing, to enrollment of multicenter clinical trials, to longitudinal cohort studies, your expertise will be essential to the quality improvement of our research process.
Community Regional Medical Center is the largest of our three main hospitals and the flagship hospital of the Central Valley. This academic-affiliated, Level 1 Trauma Center is located on a 58-acre campus in downtown Fresno. It features one of the largest and busiest emergency departments in California as well as a comprehensive burn center. Our hospital serves 2.5 million people within 9 counties, averaging a daily census of 641 patients.
Because we know our ability to provide the highest level of care begins with our incredible staff, we provide excellent benefits. On top of competitive pay, hearty retirement plans, and other core benefits, we provide extras like free concierge services to run your errands while you work, on-demand well-being, a free employee gym with free personal training, and more.
Your Career at Community | Opportunity. Challenge. Growth.
Responsibilities:
In your role, you will:
Participate in the development of accurate source material for training with other clinical departments as required. Prepare and maintain all IRB documentation, including study applications, modifications, renewals, and study closures.
Provide accurate and timely data collection, documentation, entry and reporting to both sponsor and study specific databases.
Ensure site compliance with research protocols by reviewing regulatory requirements to confirm implementation of appropriate methods, practices and procedures for all research activities. Ensure compliance with federal, state, and hospital policies and/or procedures. Provide ongoing quality control audits, including maintaining ongoing investigational drug accountability.
Communicate and collaborate specific study requirements with the PI and other research teams, including internal and external parties, sponsors, monitors, and study participants.
Monitor patients for study eligibility and assist with the informed consent process from potential research participants. Identify and report issues that may affect the accuracy and quality of the study design.
Qualifications:
Education
Bachelor's Degree in Healthcare or Health Sciences field required
Master's Degree in Healthcare or Health Sciences field preferred
Experience
1 year of research or clinical trial experience required
Licenses and Certifications
One of the following is required within 1 year of hire or transfer into position
CRA - Clinical Research Associate
CCRP - Certified Clinical Research Professional
BLS - Current Basic Life Support (BLS) for Healthcare Providers by American Heart Association (AHA) required
Disclaimers:
Please Note :
blog.nvalabs.org is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, blog.nvalabs.org provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, Site.com is the ideal place to find your next job.
We are looking for a Clinical Research Specialist to join our growing team! Working closely with the Principal Investigator, you will be responsible for clinical trials, including facilitating and coordinating daily study activities. In your role, you will consistently have the opportunity to lead our research efforts! You should possess the ability to carry out proper handling of highly sensitive information, all the while following protocol and maintaining IRB approval. From study testing, to enrollment of multicenter clinical trials, to longitudinal cohort studies, your expertise will be essential to the quality improvement of our research process.
Community Regional Medical Center is the largest of our three main hospitals and the flagship hospital of the Central Valley. This academic-affiliated, Level 1 Trauma Center is located on a 58-acre campus in downtown Fresno. It features one of the largest and busiest emergency departments in California as well as a comprehensive burn center. Our hospital serves 2.5 million people within 9 counties, averaging a daily census of 641 patients.
Because we know our ability to provide the highest level of care begins with our incredible staff, we provide excellent benefits. On top of competitive pay, hearty retirement plans, and other core benefits, we provide extras like free concierge services to run your errands while you work, on-demand well-being, a free employee gym with free personal training, and more.
Your Career at Community | Opportunity. Challenge. Growth.
Responsibilities:
In your role, you will:
Participate in the development of accurate source material for training with other clinical departments as required. Prepare and maintain all IRB documentation, including study applications, modifications, renewals, and study closures.
Provide accurate and timely data collection, documentation, entry and reporting to both sponsor and study specific databases.
Ensure site compliance with research protocols by reviewing regulatory requirements to confirm implementation of appropriate methods, practices and procedures for all research activities. Ensure compliance with federal, state, and hospital policies and/or procedures. Provide ongoing quality control audits, including maintaining ongoing investigational drug accountability.
Communicate and collaborate specific study requirements with the PI and other research teams, including internal and external parties, sponsors, monitors, and study participants.
Monitor patients for study eligibility and assist with the informed consent process from potential research participants. Identify and report issues that may affect the accuracy and quality of the study design.
Qualifications:
Education
Bachelor's Degree in Healthcare or Health Sciences field required
Master's Degree in Healthcare or Health Sciences field preferred
Experience
1 year of research or clinical trial experience required
Licenses and Certifications
One of the following is required within 1 year of hire or transfer into position
CRA - Clinical Research Associate
CCRP - Certified Clinical Research Professional
BLS - Current Basic Life Support (BLS) for Healthcare Providers by American Heart Association (AHA) required
Disclaimers:
- Pay ranges listed are an estimate and subject to change.
- Per the CDPH order, all healthcare workers are required to be vaccinated for COVID-19 or have an approved exemption and test regularly.
- If any bonuses are noted, they are only applicable to external hires meeting criteria.
Please Note :
blog.nvalabs.org is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, blog.nvalabs.org provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, Site.com is the ideal place to find your next job.