Description du poste

Celerion, leader en recherche clinique, recherche un professionnel. Rejoignez un environnement stimulant et dynamique, sans tracas d’assurance.TâchesAssurer la sécurité des participants dans le cadre des essais cliniques.Former le personnel et maintenir la conformité aux règles de l’entreprise.Produire des données d’études précises et en temps voulu.CompétencesDiplôme de praticien infirmier ou assistant médical requis.Expérience en recherche clinique appréciée.Capacité à travailler en équipe et à respecter les délais.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.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.nEssential FunctionsMaintain timely compliance with Celerion’s SOPs, required study documents, and other study- specific mandatory trainingsAssist with training of new staff upon achieving personal proficiency in required skills and tasks.Create a friendly and welcoming environment to study participantsProduce accurate and timely study data while ensuring participant safetyPre-studyParticipate in the ICF process by answering any volunteer questions about the study, in collaboration with the investigator as needed.Conduct screening physical examinationsReview subject screening data, including subject medical histories, ECGs, laboratory studies, and any other ancillary tests as outlined by the study protocol.Make preliminary eligibility decisions based on protocol inclusion and exclusion criteria.Counsel participants regarding abnormal tests and make referrals in collaboration with the investigator as necessaryAttend Sponsor SIVsAssist 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 protocolProvide training to clinic associates as neededResolve queriesDuring studyReview safety-related data including ECGs, AEs, laboratory data or other ancillary tests in a timely mannerConduct physical examinationsPerform minor procedures as outlined by the protocol following completion of required trainingEngage with client in-person (on-site) or via written, electronic or telephone correspondence to address any medical-related issuesEnsure 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 requiredAssist in referring participants to specialists as necessaryReview of outside medical records if requested by the investigatorReview of SUSAR reports if requested by the investigatorResolve queriesPost-studyReview safety-related data including ECGs, AEs, laboratory data or other ancillary tests in a timely mannerConduct physical examinationsResolve queriesKnowledge/ Skills/ Education/ LicensesSchedule; 30 hrs/week; mornings Mon-Fri; weekend rotation availabilityNurse Practitioner or Physician Assistant licenserequiredHold a DEA certificate for schedule II medications or willing to obtain upon hireTraining in Basic Life Support and Advance Cardiac Life Support, or willing to obtain upon hireBoard certified or board eligible in a primary care specialty, i.e. family practice, internal medicine, E.R. medicine or as a PA-C or NP3-5 years medical experience and / or clinical research experienceClinical research experience preferredThis isnota remote position.nCelerion Values:       Integrity   Trust   Teamwork   RespectCelerion 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. Lire la suite