What are the responsibilities and job description for the Clinical Research Sub-Investigator (NP/DNP/PA) position at Prime Clinical Research, Inc.?
We are seeking a skilled and part-time nurse practitioner or PA to join our team at Prime Clinical Research 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 8.5hr 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 Prime Clinical Research Inc’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 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 nursing license or PA license
Job Types: Part-time, Contract
Pay: $60.00 per hour
Expected hours: 10 – 15 per week
Work Location: In person
Salary : $60