A company is looking for a Contract Senior Study Start-Up Specialist responsible for overseeing and leading study start-up activities in collaboration with clinical research stakeholders. Key Responsibilities Execute start-up activities and ensure compliance with regulatory requirements Prepare and obtain approvals for Informed Consent Forms and manage ongoing submissions Collaborate with Clinical Trial Managers to track site activations and manage study budgets and contracts Required Qualifications University Degree or equivalent, preferably in a medical/science-related field 8+ years of related experience in clinical trials management Demonstrated knowledge of ICH guidelines Experience in managing projects related to clinical research Understanding of local regulatory and ethical requirements for clinical trials
Confidencial
We are Employment Pro Limited ©, a search engine for classified ads. The service aggregates and analyses jobs from different sources publicly available on the internet
We use cookies. If you continue to use this site, we understand you AGREE with that. Please review our policy page for more information.