Sub-Investigator, NP/PA
About The Position
At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion. We are seeking an experienced Nurse Practitioner or Physician Assistant to serve as a Sub-Investigator to help us grow our Artemis Institute of Clinical Research site located in San Diego, California. We are committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.
Requirements
- Minimum of two years of experience as a licensed physician assistant, family or non-acute adult nurse practitioner treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)
- Current and unencumbered license to practice as an NP or PA in the state of California required
- Commitment and ability to deliver excellent customer service
- Excellent communication, punctual and responsible
- Extremely well organized
- Excellent verbal and written communication skills
- Trustworthy, reliable; attentive to details
- Mature and pleasant demeanor
- Willingness to learn new tasks and grow with the company
Nice To Haves
- Prior experience within the clinical research industry highly preferred
- Excellent professional communication, punctual and responsible
- Friendly and outgoing demeanor
- Must demonstrate a passion for direct patient interaction
- Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team
Responsibilities
- Ensure the safety and welfare of each study subject
- Have in-depth knowledge of all research protocols
- Screen potential study subjects according to the protocol’s specific inclusion and exclusion criteria
- Conduct medical history interviews and physical examinations throughout the subject’s study participation
- Review EKG’s and lab results
- Provide medical care as needed during a subject’s participation in a clinical trial
- Provide home based on-call availability per site policy
- Attend Investigator Meetings on behalf of Principal Investigator as needed
Benefits
- Flexible Schedule
- Dynamic Team Environment
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
