Global Vigilance Coordinator Regions and Countries, DE - M
- Employer
- ClinChoice
- Location
- Germany
- Salary
- Competitive
- Start date
- 11 Oct 2019
- Closing date
- 17 Oct 2019
View more
- Discipline
- Clinical Research, Pharmacovigilance
- Hours
- Part Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Job Title: Global Vigilance Coordinator Regions and Countries - M
Location: Munich, Germany
Start: Per Candidate Availability
Contract: Permanent
TalentSource is currently looking for one Global Vigilance Coordinator Regions and Countries to strengthen the Global R&D Unit at one of our TOP Pharmaceutical client Companies in Munich, Germany.
Primary Responsibilities
- You will act as global vigilance coordinator for regions and countries and coordinate the global vigilance Sponsor Safety Organization
- You take the lead in all vigilance communications to regional Quality & Regulatory Assurance heads and Sponsor Safety Organization (information and answering questions), except for individual case management
- You will be responsible for developing and executing Global Vigilance Training and for managing solicited sources like Medical Reports. Develop processes, review and classify projects/studies, advise and train people starting up projects
- You will develop and maintain the interface between global senior vigilance division and regional Quality & Regulatory Affairs/ Sponsor Safety Organization and ensure alignment with EMEA Regulatory and with the regional Quality & Regulatory Affairs head/country Quality & Regulatory Affairs manager together
- You are Subject Matter Expert for internal vigilance audits. Supporting the Sponsor Safety Organization pre and post audit. Responsible for authority inspection readiness pharmacovigilance for Sponsor Senior Organization. Support the Sponsor Safety Organization pre and post inspection. Participate on site when needed
- Furthermore, you are overall responsible for developing, managing and classifying vigilance third party vendor agreements
Professional Experience / Qualifications
- You have a pharmaceutical university degree in science or corresponding preferably M.Sc. or PhD. and very deep experience in pharma or medical device vigilance or clinical work
- You are organised, structured and self-motivated
- You act as team leader for the Pharmacovigilance team
- You are good in engaging people
- You are interested in IT and data handling
- You are good in communication with people at all level
- You are fluent in English
If you would like to discuss the role before applying through the website, please contact alexander.sourounis@cromsource.com
Why choose TalentSource Life Sciences/CROMSOURCE?
TalentSource Life Sciences is a fully dedicated flexible resourcing department at CROMSOURCE, a family owned international, full-service Contract Research Organisation. CROMSOURCE comes from the merger of MSOURCE and CROM and we have been supporting clients with outstanding clinical research and resourcing services since 1994. Successful growth has been achieved by putting high quality and client focus at the heart of everything we do and we are proud to partner with industry leading Pharmaceutical, Biotechnology, Medical Device and Marketing Communications worldwide.
Our employees are the most valuable company asset and because we want to retain our staff, we ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel clear tools to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our current below industry average turnover rates.
Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are experts providing experts - highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world.
Skills: Junior Pharmacovigilance officer, Pharmacovigilance Manager, Pharmacovigilance Scientist Location: Germany Share:
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Company
ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.
We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
- Website
- https://clinchoice.com/
- Telephone
- +44 1628 566121
- Location
-
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom
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