CRA 2, Internal Medicine, Biotech
Cette offre est-elle pour vous ?
Créer mon CV Créez votre CV et découvrez votre pourcentage de correspondance avec ce poste — et avec tous les autres.
Le poste
Conduct site visits including site selection, initiation, monitoring, and close-out to ensure trials are executed per protocol.
Ensure ongoing trial conduct aligns with GCP, ICH guidelines, and sponsor requirements.
Coordinate communications with site staff, resolve queries, and manage issue escalation.
Verify source data, maintain essential regulatory documents, and support regulatory submissions as needed.
Collaborate with cross-functional teams to uphold data quality and patient safety.
Identify risks, implement corrective actions, and contribute to trial timelines and milestones.
Ensure ongoing trial conduct aligns with GCP, ICH guidelines, and sponsor requirements.
Coordinate communications with site staff, resolve queries, and manage issue escalation.
Verify source data, maintain essential regulatory documents, and support regulatory submissions as needed.
Collaborate with cross-functional teams to uphold data quality and patient safety.
Identify risks, implement corrective actions, and contribute to trial timelines and milestones.
Voir l'offre en entier
Missions, profil recherché, compétences et avantages — en créant votre compte gratuitement.
ou
Déjà un compte ?
Se connecterOffres similaires
D'autres postes qui pourraient vous convenir.
? Senior Data Scientist ? Physician, Primary Care - Long Beach, CA ? LVN I (Bilingual) - Internal Medicine - Full Time ? Medical Assistant - Full-Time - Internal Medicine ? Medical Assistant - Internal Medicine Hematology-Oncology - Oak Park 24057 ? Primary Care Physician - Internal Medicine (Resident Trained) – Chicago Streeterville Campus