What are the responsibilities and job description for the Nurse Practitioner or Physician Assistant position at Headlands Research?
Join Us in Improving Lives through Clinical Research
At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20 clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.
Championing Diversity in Clinical Trial
sDiversity 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 Lifeti
meAre you ready to make a difference? We're seeking an experienced Nurse Practitioner or Physician Assistant to serve as a Sub-Investigator to help us grow our Trial Management Associates site located in Myrtle Beach, South Carolina. Ideally, we are seeking someone for either a full-time or part-time positio
n.
Why Join
- Us?Dynamic Team Environment: You'll help Headlands Research continue to build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlan
ds.
Type: Full-time Employee (40 hours/w
eek)Pay: Competitive and dependent upon years of experience as an Investigator in clinical resea
rch.Location: Onsite in Chesterfield, MO (no opportunities for remote or hyb
rid)
Responsibili
- ties:Ensure the safety and welfare of each study su
- bjectHave in-depth knowledge of all research prot
- ocolsScreen potential study subjects according to the protocol’s specific inclusion and exclusion cri
- teriaConduct medical history interviews and physical examinations throughout the subject’s study particip
- ationReview EKG’s and lab re
- sultsProvide medical care as needed during a subject’s participation in a clinical
- trialProvide home based on-call availability per Artemis standard p
- olicyAttend Investigator Meetings on behalf of Principal Investigator as n
- eededExcellent professional communication, punctual and respon
- sibleFriendly and outgoing dem
- eanorMust demonstrate a passion for direct patient intera
- ctionDemonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary
team
Qualifica
- tions:Minimum of one year 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 med
- icine)Current and unencumbered license to practice as an NP or PA in the state of Missouri re
- quiredPrior experience within the clinical research industry highly pre
- ferredCommitment and ability to deliver excellent customer s
- erviceExcellent communication, punctual and respo
- nsibleExtremely well org
- anizedExcellent verbal and written communication
- skillsTrustworthy, reliable; attentive to d
- etailsMature and pleasant de
- meanorWillingness to learn new tasks and grow with the c