We are hiring for a Sub Investigator in San Bernardino, CA. We are looking for an experienced Nurse Practitioner OR Physician Assistant for an established clinical research site. Amazing opportunity to get into research, or for those that are experienced to set foot with a large and well known research organization. Apply today!
MUST be bilingual in Spanish!
Summary:
The Sub Investigator has responsibility for the clinical safety of the patients partaking in the clinical trial, collecting, and recording accurate clinical data while also ensuring that the well-being and interests of the subjects enrolled in the studies are being met. Under the direction of the Principal Investigator, responsibilities will include, identify and recruitment of participants, obtaining informed consent, management of protocol related procedures, participate in study visits, communicate with families, participants, referring physicians and other health care providers. Educating and guidance to participants and families to ensure compliance and retention of study participants, tracking and recording of adverse events, performing physical exams to ensure enrollment criteria and to track for any changes during study participation.
Role & Responsibilities:
- Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and SOPs
- Ensure the safety of study participants, and maintain 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, as needed, 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 (e.g. 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.
- Other duties as assigned
Education and Experience:
- Must be a Licensed Nurse Practitioner or Licensed Physician’s Assistant in the state in which you are practicing.
- Previous experience with Clinical Trials highly preferred
Schedule: 100% ON SITE, 30 hours per week; candidate preferences taken into consideration.
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. Eligibility for health benefits is based on verifying that an average of 30 hours per week during the first 4 weeks of the work assignment has been met. If you meet eligibility requirements and take action to enroll, you will be covered no earlier than 60 days into your assignment, depending on plan selection(s).)
- 401k (eligible on the first 401k open enrollment date following 6 consecutive months on assignment. 401k Open Enrollment dates are 1/1, 4/1, 7/1, and 10/1)
- 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, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).
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. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
