Clinical Programmer

🕒 il y a 2 mois

🐎 Kentucky – Distant

🐎 Kentucky – Remote

⏰ Temps Plein

🟢 Junior

🖥 Ingénieur Logiciel

Postuler Maintenant

Trouver des Emplois à Distance Similaires

Recevoir des emails pour des emplois à distance

📊 Vérifiez votre score de CV pour ce poste

Améliorez vos chances d'obtenir un entretien en vérifiant votre score de CV avant de postuler.

Télécharger le CV

CTI Clinical Trial and Consulting Services

Site WebLinkedInTous les Emplois

1001 - 5000 employés

Fondée en 1999

🧬 Biotechnologie

💊 Pharmaceutique

Biotechnology • Pharmaceuticals

CTI Clinical Trial and Consulting Services est une organisation de recherche sous contrat (CRO) à service complet qui offre l'exécution d'essais cliniques, une stratégie réglementaire, des services de laboratoire et bio-analytiques, la génération de preuves du monde réel et la gestion de centres de recherche pour les promoteurs biotechnologiques et pharmaceutiques. Avec une expertise couvrant les études de phase I à IV et des domaines thérapeutiques complexes (y compris les maladies rares, la thérapie cellulaire et génique, l'oncologie, la neurologie et la transplantation), CTI soutient la conception d'études, la gestion de sites, le recrutement de patients, la surveillance, la sécurité/pharmacovigilance, la biométrie et l'assurance qualité. Basée à Covington, KY, l'entreprise met l'accent sur des approches intégrées et centrées sur le patient et sur l'orientation réglementaire mondiale pour accélérer le développement et apporter des thérapies aux patients.

Description

• Act as a primary database architect for client clinical databases using Medidata Rave, OmniComm TrialMaster, or other database applications as needed for Clinical Trials • Create database entry screens based on approved case report form (CRF) casebook • Perform internal testing of entry screens prior to user acceptance testing • Work with lead CP or Study Clinical Data Manager to implement system edits on built entry screens • Program validation procedures, in conjunction with the Sr. CP or CP II, for clinical studies and other billable projects. • Maintain necessary study build documentation as required by CTI SOPs • Meet all project deadlines on time and on budget • Ensure accuracy of clinical databases as compared to the CRF; perform user acceptance testing (UAT) of database and provide feedback to study team regarding any discrepancies • Perform UAT on programmed edits in the clinical database; ensure accuracy of edits in database as compared to edit specifications documents; provide feedback to study team on functioning of edits. • Perform review and issue queries for CRF data, based on automated edit checks, manual review, post-hoc data listings, and sponsor requirements • Maintain all necessary data review documentation to support accurate data cleaning.

🎯 Exigences

• Bachelor’s degree or equivalent experience in Computer Science/Information Technology or a technical degree in a related field • 1+ years of experience working with databases in a complex clinical data management (CDM) environment, and/or equivalent combination of education and experience • Database experience with OmniComm TrialMaster or Medidata Rave is preferred

🏖️ Avantages

• Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. • We also value ongoing education and training through tuition reimbursement and a dedicated training department. • Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. • We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. • We also encourage care for the world around us through our unique CTI Cares program.