Subinvestigator - Nurse Practitioner/ Physician Assistant - PRN
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Before you apply
LocationOmaha, NE
Work modeon-site
Typepart-time
SeniorityMid
Experience3–5 yrs
DepartmentJob Posting Categories, Clinical Research
Company size501–1,000 people
PostedMay 28, 2025 · 1y ago
Verified live2d ago
May no longer be actively hiring
Posted by the company on May 28, 202556% of this company's open roles have been listed for 90+ days
At a glanceSummarised by Seekless from the posting.
Nurse Practitioner or Physician Assistant license required
Hold a DEA certificate for schedule II medications or willing to obtain upon hire
Training in Basic Life Support and Advance Cardiac Life Support, or willing to obtain upon hire
Board certified or board eligible in a primary care specialty, i.e. family practice, internal medicine, E.R. medicine or as a PA-C or NP
3-5 years medical experience and / or clinical research experience
Clinical research experience preferred
About the company
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
About the role
Do you have a flexible schedule and enjoy a fast paced environment? Say goodbye to insurance hassles and late-night charting.
Join the exciting world of clinical trials. Be at the forefront of a new drug’s journey to market.
Ensure the safety of healthy volunteers in Phase One Research Clinic.
Essential Functions
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Maintain timely compliance with Celerion’s SOPs, required study documents, and other study- specific mandatory trainings
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Assist with training of new staff upon achieving personal proficiency in required skills and tasks.
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Create a friendly and welcoming environment to study participants
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Produce accurate and timely study data while ensuring participant safety
Pre-study
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Participate in the ICF process by answering any volunteer questions about the study, in collaboration with the investigator as needed.
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Conduct screening physical examinations
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Review subject screening data, including subject medical histories, ECGs, laboratory studies, and any other ancillary tests as outlined by the study protocol.
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Make preliminary eligibility decisions based on protocol inclusion and exclusion criteria.
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Counsel participants regarding abnormal tests and make referrals in collaboration with the investigator as necessary
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Attend Sponsor SIVs
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Assist in the logistical setup of new studies by collaborating with the nursing department and working with study management to ensure the successful execution of all medical aspects of the protocol
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Provide training to clinic associates as needed
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Resolve queries
During study
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Review safety-related data including ECGs, AEs, laboratory data or other ancillary tests in a timely manner
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Conduct physical examinations
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Perform minor procedures as outlined by the protocol following completion of required training
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Engage with client in-person (on-site) or via written, electronic or telephone correspondence to address any medical-related issues
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Ensure safety of study participants by reviewing and managing adverse events and serious adverse events under the supervision of the PI. Perform assessments and administer necessary treatment when required
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Assist in referring participants to specialists as necessary
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Review of outside medical records if requested by the investigator
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Review of SUSAR reports if requested by the investigator
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Resolve queries
Post-study
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Review safety-related data including ECGs, AEs, laboratory data or other ancillary tests in a timely manner
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Conduct physical examinations
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Resolve queries
Knowledge/ Skills/ Education/ Licenses
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Schedule includes one weekday based on candidate preference; approximately 8 hours per week
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This position will work onsite at our Omaha, NE screening location.
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Nurse Practitioner or Physician Assistant license required
•
Hold a DEA certificate for schedule II medications or willing to obtain upon hire
•
Training in Basic Life Support and Advance Cardiac Life Support, or willing to obtain upon hire
•
Board certified or board eligible in a primary care specialty, i.e. family practice, internal medicine, E.R. medicine or as a PA-C or NP
•
3-5 years medical experience and / or clinical research experience
•
Clinical research experience preferred
Celerion Values: Integrity Trust Teamwork Respect
Legal
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
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