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Form of workNational Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a Physician Assistant/Nurse Practitioner with 2 or more years of experience.
As a Physician Assistant or Nurse Practitioner you will be at the forefront of clinical research, supervising and driving the success of clinical trials.
($200 per patient visit / up to 1 hour visit)
Responsibilities:
Your primary and key responsibilities include:
Promoting and upholding Good Clinical Practices (GCP) and ensuring the smooth execution of clinical investigations.
Guardian of patient rights, data integrity, and protocol compliance, ensuring that our clinical trials meet and exceed regulatory standards and industry best practices;
Ensure the safety and well-being of our research participants
This involves reviewing laboratory results, conducting vital sign assessments, and monitoring safety tests, among other critical tasks
Other responsibilities include:
Supervise the clinical activities for the clinical trial they are assigned.
Responsible for recording and meticulously following up on adverse events, demonstrating your commitment to subject welfare.
Role will involve making crucial trial-related decisions, helping to guide the course of our clinical trials to successful outcomes.
Uphold strict adherence to study protocols, verifying that our research results are reliable and meaningful.
Verify that all requirements for obtaining informed consent are met, respecting the rights and autonomy of our research subjects.
Perform physical examinations, take detailed medical histories, and conduct reviews that contribute to the comprehensive understanding of each patient's health status.
Be available on-site for protocol-required surveillance and remain on-call to address medical events as they arise.
Play an active role in sponsor visits and regulatory audits, showcasing your dedication to compliance and quality research.
Additional duties/responsibilities include:
Record all study-related events with impeccable compliance to GCP, ensuring the accuracy and transparency of our records
Review study protocols and standard operating procedures (SOPs) to stay aligned with the latest research practices
Complete and review regulatory documents as required, showcasing your commitment to compliance
NICR is an independent, multi-site clinical trial management organization (SMO). We deliver and facilitate the highest quality clinical trial management to our multi-specialty network of affiliated physicians and researchers across California and Texas.
Location
Bakersfield, CA
Employment Type
Part-Time
This is not a remote position
