Company: Clinical Professionals Ltd
Closing Date: 18 Feb 17
Type: Full Time
Salary (£): On Application
Benefits: Competitive, plus company car and benefits
A global Medical Devices company based in Belgium is seeking individuals with Clinical Study design/implementation experience. Do you have solid working experience within the clinical study management or clinical project management?
Associate Clinical Study Manager
Employment Type: Permanent, full-time
Salary: Competitive, plus company car and benefits
We are currently working with a global Medical Devices company based in Belgium who is seeking individuals with Clinical Study design/implementation experience. Do you have solid working experience within the clinical study management or clinical project management or even strong background as a lead CRA within the Medical Devices industry? If yes then this new position is made for you!
Key tasks and responsibilities:
*Designing, implementing and managing clinical projects and the assigned clinical areas;
*Providing scientific support to the clinical projects, as well as managing clinical trials so that they comply with local/national/international regulatory requirements;
*Participation in budget forecasting and preparation, ensuring that timelines are successful met and ensuring budgetary restrictions are observed;
*Identification and promotion of strategies for the improvement of the quality of clinical research, as well as for the improvement of best practices in the clinical research department;
*Proactive assessment of clinical project progression and development of strategic responses to identified issues and trends.
*Interpreting study results and preparing summaries in preparation for regulatory submissions/publication;
*Liaising with study investigators in order to provide oversight for papers, presentations and meetings which involve the presentation of clinical data;
*Personnel management, to involve the leadership of research staff, management of resources and provision of guidance and support to direct reports regarding research priorities;
*Encouragement of career growth and provision of training for new/existing clinical personnel.
*BSc in Life Sciences, Bioengineering, or other biology-related degree;
*Solid experience in the clinical research environment medical devices is requested;
*Proven experience in direct study management (medical devices, ideally Class III);
*Knowledge of clinical trial regulations and the ability to demonstrate applicable leadership skills.
Extra/beneficial knowledge and skills:
*Level of English language to mother tongue standard is a must, as well as one other European language; if you do speak Flemish to a professional level that will be a major plus;
*Excellent knowledge of clinical software;
*Strong communication, project management and budgeting skills.
If this role would be of interest to you, and you possess the required skills and experience, please contact Yasmina Mallem on +32 2 892 3993 for an informal discussion.
If you do not feel that this is the right role for you, please do not hesitate to forward these details on as we have a generous referral scheme in place.
Medical devices; cardiovascular; active devices; pharmaceutical; biotechnology; clinical; research; clinical research; Belgium; English; French; Flemish; Dutch; German; project management; budgeting; regulatory; health sciences; Life Sciences; biostatistics; study management; clinical project.
Clinical Professionals UK
33 Blagrave Street
|Tel:||0044 118 959 4990|
|Fax:||0044 118 956 0607|
|Website:||Visit Our Web Site|
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