Physician Assistant / Nurse Practitioner

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:

• 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