Full Job Description
National 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. ($150 per patient visit / up to 1 hour visit) Responsibilities: Your primary and key responsibilities include:
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- 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 comprehensively understand 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 with 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
- San Antonio, TX
Employment Type
- Part-Time
- This is not a remote position