Beschreibung
Aufgabe:- Manage a specified trial or group of trials, working with SMs, CTAs and others to ensure compliance with the protocol Company SOPs, ICH-GCP and local regulatory requirements, local productivity targets and financial agreements
- Perform all trial-specific duties and activities for the trials for which he/she is responsible according to the current list of Roles and Responsibilities
- Act as the primary local Company contact point for trial-related items
- Coordinate and/or perform trial-specific training for local Company and investigational site staff
Anforderung:
- Medical, para-medical or other biologically related scientific education at university level.
- Experience and proficiency in the conduct and management of clinical trials
- Clinical Drug Development: thorough understanding of clinical drug development and regulatory procedures and processes
- Leadership and Teamworking: Ability to manage and support the activities of local staff assigned to the trials for which responsible
- Managing workloads: ability to organise multiple complex priorities and projects and use a range of techniques to identify and resolve trial-related problems
- Decision making : ability to solve complex local trial-related situations
- high level of fluency within the english language
Beginn: 18.05.2015
Dauer: 13.12.2015
Branche: Medizin/Healthcare