Nurse Practitioner - Clinical Research

Headlands Research•Chesterfield, MO

4d•Onsite

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. Championing Diversity in Clinical Trials Diversity isn't just a checkbox for us - it's central to our mission. We're 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. The Role of a Lifetime Are you ready to make a difference? We're seeking an experienced Nurse Practitioner or Physician Assistant to help us grow our clinical research site located in the Greater St. Louis Area. You will help the site conduct clinical research trials involving gastroenterology, neurology, vaccines, and general internal medicine. Clinical Research Professionals (CRP) is a dedicated research center that provides a network of providers who work collaboratively in conducting clinical research trials. The site’s team brings more than 20 years of experience, including many highly accomplished principal investigators across multiple therapeutic areas that are helping to improve lives through advancement of new drug therapies and medical devices.

Requirements

Minimum of two years of experience as a licensed family or non-acute adult nurse practitioner or physician assistant 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 Missouri required
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
Commitment and ability to deliver excellent customer service

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 standard policy
Attend Investigator Meetings on behalf of Principal Investigator as needed
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