Beschreibung
Local Trial Manager - Senior (m/f/d)
Reference: -en
Start: 01/20
Duration: 9 MM++
Main tasks:
- Manage a specified trial or group of trials within the territory of Belgium, the Netherlands and Luxemburg, 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 (see attached)
- Act as the Global Trial Manager
- Primary local Company contact point for trial-related items
- Partner with Site Manager(s), Clinical Trials Assistant(s) and other local trial-related roles to ensure successful site management
- Review contact reports from Site Managers and take corrective action as necessary
- Coordinate and/or perform trial-specific training for local Company and investigational site staff
Main qualifications
- Education - 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 within GCO
- Leadership and Teamworking - ability to manage and support the activities of the Site Managers and other 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
- Coaching - Understand and apply coaching theory and skills and select appropriate coaching structure to suit individual needs
- Decision making - ability to solve complex local trial-related situations
- Interpersonal Skills - Excellent spoken and written Swiss German, French and English, good presentational and motivational skills
- Computer skills - Understand and use a range of computer-based systems to track, monitor and report on investigational site and local trial activity and status
- Procedures and Processes - Possess a comprehensive knowledge of and comply with Company SOPs, ICH-GCP, (where appropriate, European) and local national regulations
- Willingness to travel with occasional overnight stay away from home
Main advantages:
- Varied tasks in a renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Marc-Sebastian Heftrich
Referencenumber:
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