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Clinical Research Physician Assistant
1 month ago
We are seeking a highly skilled and experienced Sub Investigator to join our team at Medix™ in San Bernardino, CA. As a key member of our clinical research site, you will be responsible for ensuring the clinical safety of patients participating in clinical trials, collecting and recording accurate clinical data, and ensuring the well-being and interests of study participants are met.
Key Responsibilities:
- Conduct and manage clinical trials in accordance with study protocols, GCP, ICH Guidelines, and SOPs
- Ensure the safety of study participants and maintain effective communication with patients
- Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols
- Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
- Oversee and administer medications and treatments per study protocol and scope of practice
- Assess, grade, and document adverse events; apply triage and judgment to determine course of action
- Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols
- Ensure good documentation practices are applied by team members when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries
- Ensure confidentiality of patient protected health information, sponsor confidential information, and company confidential information
- Evaluate potential subjects for participation in clinical trials, including phone and in-person prescreens
- Create and execute recruitment strategies in conjunction with patient recruitment staff
- Incorporate key timelines, endpoints, required vendors, and patient population when planning for each assigned protocol
- Perform clinical duties, such as drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing, within scope
- Comply with institutional policies, standard operating procedures, and guidelines; prepare and submit documentation as required by the study protocol and study sponsor; interpret complex protocols
Requirements:
- Must be a Licensed Nurse Practitioner or Licensed Physician's Assistant in the state in which you are practicing
- Previous experience with clinical trials is highly preferred
Benefits:
- Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances)
- Health Benefits / Dental / Vision (Medix Offers 6 different health plans: 3 Major Medical Plans, 2 Fixed Indemnity Plans (Standard and Preferred), and 1 Minimum Essential Coverage (MEC) Plan)
- 401k (eligible on the first 401k open enrollment date following 6 consecutive months on assignment)
- Short Term Disability Insurance
- Term Life Insurance Plan
Further Information:
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws.
This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment.
