Clinical Research Licensed Practical Nurse Lpn H/F Biotrial
- États-Unis
- CDI
- Bac
- Bac +2
- Service public hospitalier
- Exp. 1 à 7 ans
Les missions du poste
Responsibilities:
- Develop a high level of familiarity and knowledge of the study protocol and flow chart of study procedures.
- Implement study procedures in compliance with accepted research guidelines including Health Insurance Portability and Accountability Act (HIPAA) regulations and the study protocol.
- Participate in the review and validation of the study CRFs in conjunction with the Investigator, Clinical Research Nurse, and the Clinical Research Associate of the Study.
- Perform study procedures (e.g., participate in screening procedures, prepare and administer infusions under the supervision of a pharmacist or physician, start intravenous lines, venipunctures, obtain biological specimen samples, obtain ECG recordings, vital signs, safety assessments, etc., and pharmacodynamic measures - psychometric tests, etc.), process blood samples as required by study protocol under the supervision of the Principal Investigator.
- Record study data in the source documents. Evaluate and review study data to ensure accuracy and completeness.
- Assist in transcribing study data from source documents to sponsor designated case report forms or record data for remote data entry if applicable.
- Resolve data queries in conjunction with the sponsor.
- Assist the Principal Investigator with gathering and recording relevant data for adverse event reporting and expedited reporting of serious adverse events to the sponsor.
- An active LPN license in the State of New Jersey and IV experience preferred, but not required.
- Minimum of 3 years' experience as a LPN.
- Knowledge of FDA regulatory requirements is necessary, ex. CITI
- Excellent communication skills with the ability to interact with the Principal Investigator, Sub-Investigators, Biotrial Clinical Project Team and Sponsor personnel.
- Excellent communications skills with ability to interact with Sub-Investigators, Project Team and Sponsors.
- Good working knowledge of Microsoft Office Suite including Word and Excel.
- Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
- Ability to speak effectively before sponsors, patients and employees of organization.
- Knowledgeable of clinical research process preferred but not required.
- Ability to work independently, efficiently and accurately with high productivity.
- Experience in conducting complex long-term projects and meeting strict timelines.
- Good interpersonal skills.
- RTT - JNT
- Carte tickets restaurants
- Accord d'intéressement
- Horaires flexibles
- Entreprise bretonne à taille humaine basée à l'international
- Parcours d'intégration pour les nouveaux arrivants
- Accessibilité en transports en commun et parking privés
- Belles opportunités de carrière
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Paid time off
- Referral program
- Vision insurance
Les étapes de recrutement
Les étapes de recrutement peuvent varier selon l'offre à laquelle vous postulez.
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Premier contact téléphonique par notre service RH.
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Entretien avec vos futurs collègues et le service RH.
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Suivant le poste, vous pourrez réaliser une évaluation de personnalité professionnelle.
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Le poste vous convient ! Nous préparons votre intégration.
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Biotrial en images
Salaire fourni par le recruteur
Publiée le 09/10/2025 - Réf : 3557986/25767346 CRLPNL/N
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Clinical Research Licensed Practical Nurse Lpn H/F
- États-Unis
- CDI
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