Clinical Research Spec.
Clinical Research Spec.
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Salary Not Disclosed
1 Vacancy
Job Description
Overview
*Hybrid 1 day remote Fresno*
Opportunities for you!
- Consecutively recognized as a top employer by Forbes
- Vacation time starts building on Day 1 and builds with your seniority
- 403(b) retirement plan with up to 8% matching contributions
- Free parking and electric charging
- Great food options with ondemand ordering
Commitment to diversity and inclusion is a cornerstone of our culture at Community. All are welcome as valued members of our community.
We know that our ability to provide the highest level of care is through taking care of our incredible teams. Want to learn more Click here.
Your Career at Community Opportunity. Challenge. Growth.
Responsibilities
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.
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
- Bachelors Degree in Healthcare or Health Sciences field required
- Masters Degree in Healthcare or Health Sciences field preferred
Experience
- 1 years 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.
If any bonuses are noted they are only applicable to external hires meeting criteria.
Employment Type
Unclear
