Job Description

Job Description

Job Description

We are seeking a skilled and part-time nurse practitioner or PA to join our team at Patient First Clinical Trials (PFCTRIALS) as a sub-investigator. The ideal candidate should have a strong background in their specialized clinical practice, with experience in clinical research. The sub-investigator will play a crucial role in providing exceptional patient care, performing trial-related procedures including physical exams, administering scales, recording data, and contributing to the smooth execution of research. This position offers an opportunity to make a meaningful impact on patients' lives and contribute to advancements in medical research.

Why us?

● A great team of clinical and non-clinical staff to work with

● Get mentored directly/mentored by an amazing Investigators and team.

What doing a great job will look like

● Seeing an average of 6 - 10 patient's visit per 8hr day.

● Maintaining turnaround times of an hour or less 80% of the time (from patient in door time to patient out the door).

● Building a full patient panel consistently.

● Being a good team player

● Aligning with culture of the organization and following leadership of the Supervisor

● Having a great attitude that is friendly and welcoming to Team members and patients

We will help you do a great job through these trainings through the Patient First Clinical Trials (PFCTRIALS)'s Onboarding process.

● How to see 6-10 patients' visit per day and leave with no source documentation tasks incomplete.

● How to build your clinical research career through networking and coaching.

● How to have work-life balance

● How to get 5-star patient ratings and increase patient satisfaction

● How to multi-task and efficiently use the different systems in clinical research

● How to manage patient's schedule daily and efficiently.

This opportunity is perfect for the Sub-Investigator who:

● Has a strong work ethic.

● Is willing to learn the new skills required to thrive and a quick learner.

● Is a team player

● Is flexible

● Is eager to be teachable, correctable, coachable

This opportunity is a poor fit for sub-Investigator who is:

● not welcoming or friendly to patients

● Inflexible

● Values “me” above “we”

● A poor communicator

● Does not clean up after him/herself

● Does not make consistent effort to make sure patient's scheduling is priority.

● He/ She isn't able to learn after multiple teachings, or isn't teachable, coachable or correctable.

● Insubordinate and has a “I follow my own rules” mindset

● Encourages and instigates office drama

Responsibilities:

• Protect the safety and welfare of all trial participants.
• Ensure that participants understand the potential risks, benefits, and extent of their participation in a trial.
• Assist in conducting the trial in accordance with the protocol, SOPs, and ICH GCP.
• Assess and monitor subjects’ safety and wellbeing.
• Assist in maintaining appropriate documentation such as source records, all IRB-approved protocol and informed consent form (ICF) versions, and original signed ICFs.
• Provide medical treatment to patients as needed throughout the duration of the trial.
• Conduct study-related procedures such as vital signs, physical exams, and medical rating scales.

Requirements:

• Valid NP license

Job Types: Part-time, Contract

Medical Specialty:

• Primary Care

Work Location: In person

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