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| geplaatst door |
datum
plaatsing: |
termijn
realisatie |
budget /
salaris |
| jvdbeek |
08-09-10 13:19 |
2 tot 6 maanden |
op uurbasis |
|
|
|
|
| locatie |
reacties |
bekeken |
status |
| Almere |
7 |
563 |
gesloten |
project titel
Interim manager data management eu life science ..
afrondings toelichting
Thank you for your response.
We are sorry to inform you that the interim position is no longer vacant.
Regards, Jose van de Beek
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project omschrijving
Interim Manager Data Management EU Life Science in Almere
Project
Supervises and coordinates the (Senior) Data Managers, Medical Data Operators and Database
Programmers of the group in support of the group’s studies and other activities in
conjunction with the other managers of the department. May have other roles, like
Departmental Quality Representative.
Responsible for the budgeting, planning and resourcing of the group’s activities;
Interacts with project leaders and other stakeholders to ensure adequate support for
clinical projects and systems;
Supervises group members;
Ensures that the outsourcing of activities is well organized and that oversight is at the
required level;
Contributes to global and local departmental development projects to improve quality,
effectiveness and efficiency;
Collaborates with EU and US departments in the design and implementation of procedures,
systems and standards;
Manages own group;
May represent the unit in EU or global meetings;
Develops, implements and maintains adequate quality management standards and quality
control measures in the group, in order to improve and consolidate ‘best in class’
performances;
Ensures that group’s activities follow regulatory requirements and departmental SOPs;
May have a leading role globally in the development, revision and review of Data
Management SOPs, guidelines and Work Instructions. Is actively involved in writing and
review, but can delegate part of these activities to others in the department;
Maintains an ongoing focus on industry trends regarding opportunities and challenges;
reports on issues identified in order to improve and develop the strategy and
deliverables;
Acts as Departmental Quality Representative in EU;
Coaches and advises on quality matters;
Ensures that the department compliance records management is at the required level.
We are looking for a consultant with
Bachelors or Master’s degree in Life Sciences or equivalent
At least 3 year management experience
At least 5 year experience in Data Management in a CRO or pharmaceutical R&D, including
all phases and large studies
Experience with international complex drug development in a multicultural environment
Experience with EDC
Ability to use SQL (Standard Query Language) to generate data retrievals and in possession
of an active knowledge of ClinTrial (Data Management application)
Accuracy and attention to detail in working with clinical data
Good planning, project management and organizational skills
Working knowledge of common Data Management applications (e.g. database programs and
programming / query languages)
Analytical approach
Good people management skills
Fluent English, verbal and written
We are looking for a freelance consultant for 3 months.
Please submit you cv and tariff.
No agencies please.
Only freelance consultants
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