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| Clinical Research Associate - Munich/Karlsruhe/Nuremberg |
You will be primarily tasked to set up and monitor clinical trials
conducted in the Munich/Karlsruhe/Nuremberg as part of international projects. You should thrive
in multi-national project teams and be focused on delivering exemplary
levels of customer service.
With a life sciences degree or nursing
qualification and at least one year experience of Phase II-IV
trials, you will have in-depth knowledge of FDA and ICH GCP
requirements.
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| Senior Clinical Research Associate - Munich/Karlsruhe/Nuremberg |
| As well as carrying out the responsibilities of a CRA
as above, you will have a life sciences degree or nursing qualification and a minimum of two year's experience, including experience of start-up monitoring and close-up. As a SCRA you will have the opportunity to mentor more junior CRAs and may be asked to take on project coordination
activities as a lead CRA. |
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| Research Assistant /Project Assistant - Munich/Karlsruhe |
As a research assistant or project assistant you will provide vital support for clinical research projects. You will have excellent communication and organisational skills and a self-motivated, flexible and professional attitude. You must be able to prioritise and work well within a multi-national team environment and have an in-depth knowledge of Microsoft Word, Excel and preferably PowerPoint.
Project assistants will have a good standard of education and two years administration experience.
Research assistants will have a life science/nursing qualification and at least six months administration experience. The research assistant role will provide the training required to progress and become a clinical research associate. |
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| Associate Director, Clinical Data Management - Nuremburg |
Supporting the Vice President, Clinical Data Management you will provide management and support to all data management processes, ensuring all projects are conducted in accordance with sponsor requirements and PPD Standard Operating Procedures and within budget.
Duties and Responsibilities (according to relevant guidelines, laws and SOP’s):
- To provide general support to the European Vice President of Data Management in Europe overseeing and developing data management staff
- To participate in the formation and implementation of the strategic development plans for data management both within Europe and on a global basis.
- To support department structure through leadership of various functions within the department.
- To participate in executive review meetings and deputise for the Vice President of Data Management when required.
- To be able to identify improvement opportunities, devise a strategy and implement the necessary tactical activities to achieve the strategy.
- To ensure adherence to Company and Department policies and procedures with the group.
- To act as Line Manager to a group of Group Leaders across Europe and work on their continued development.
- To ensure that all Line Management Team work to the latest Global SOPs and WPDs and to ensure that all Line Management Teams are appropriately trained in these.
- To ensure that for each Line Management staff member that there is a training plan in place.
- To ensure that there is regular review of each individual member of the team. This should include and assessment of each individual’s contribution, their key responsibilities and training needs. In addition, to ensure that all required steps are taken to deal with non-performance of the Team as a whole, in order to identify areas where quality, efficiency and individual performance can be developed and improved.
- To manage all aspects of data management for groups of assigned clients and projects. This includes ensuring the creation and maintenance of detailed project plans for DM aspects of projects.
- To identify resource requirements by staff type at project set-up and for the duration of the project, and to ensure that the resource is in place for all assigned projects.
- To ensure that for all assigned projects the DM tasks are completed accurately, on time and within budget.
- To act as the senior contact for all aspects of data management for assigned clients and projects. This includes effectively liaising with/meeting Sponsors, Project Managers and internal department staff over progress and any technical issues.
With a Life Science Degree or equivalent you will have a minimum of 8 years experience of Data Management in the clinical research field, including 5 years management experience. An excellent track record in Strategic Management in a Data Management role is preferred, including driving the management of change to raise the performance of a Data Management activity to the highest level. Planning and budgeting experience at a senior level is a key requirement.
For more information or to apply for this position, please send your CV and covering letter in Word format to recruitdm.sm@europe.ppdi.com
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| Manager, Clinical Data Management |
You will primarily be responsible for the supervision, management, training and development for a number of clinical data management staff and will also be involved in making strategic decisions that affect the direction and function of the Clinical Data Management Department. In addition, you may take on the Clinical Data Manager role for one or more projects.
You will be educated to degree level in life sciences or a related subject, and/or have relevant clinical trials experience. In addition, as the primary focus of this exciting, senior role is line management, previous experience is essential. |
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| Clinical Data Manager - Nuremburg |
You will be responsible for running your own studies and organizing the full range of data management services in an exciting and challenging environment.
Responsibilities will include managing studies, co-ordinating a team of clinical data associates and processing technicians, resources and budgets, and assessing study activities in comparison to project milestones and timelines.
You will be educated to degree level in life sciences or a related subject and/or relevant experience. The ability to communicate effectively within the project team and to sponsors on operational issues is essential.
For more information or to apply for this position, please send your CV and covering letter to:
Human ResourcesFor more information or to apply for this position, please send your CV and covering letter to:
Human Resources
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| Clinical Data Associate - Nuremburg |
You will be responsible for performing a wide variety of data management activities from study set-up to database lock. Reporting to a Clinical Data Manager you will have the ability to work as part of a team producing high quality work within tight deadlines.
You will be educated to degree level in life sciences or a related subject/and or relevant experience. Various opportunities also exist to progress to different levels within this role.
For more information or to apply for this position, please send your CV and covering letter to:
Human Resources.
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| Project Management Opportunities |
Our sustained year on year growth at PPD means that we are looking for Project Managers to join our rapidly growing teams at our offices in Cambridge, Glasgow, Winchester, Brussels, Paris and Munich.
What is most significant about our recruitment activities is the breadth of project management experience we’re looking for. We need individuals with varying degrees of experience to take on European and Global project management, programme management and product development roles.
Our Project Managers lead and are accountable for time, cost and quality targets and resource and budget control. To achieve this, candidates must not only possess the appropriate project management experience but also the drive and enthusiasm to share and apply their knowledge to the diverse and challenging projects we manage for our clients. In return, you will have excellent career opportunities and Project Managers who fit the required profile can benefit from the option of being home or office-based. |
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| Regulatory Affairs Manager |
Due to an increase in business we are looking for Regulatory Affairs Managers to be based in our offices in Germany. You will be responsible for providing timely, accurate regulatory advice on strategy and will manage projects in the provision of regulatory affairs services. This will involve you liaising with internal and external clients in the provision and marketing of these services.
A key aspect of your role will be to provide regulatory advice on strategy and manage projects in the provision of regulatory affairs services and liaise with internal and external clients in the provision and marketing of these services for those countries of responsibility (Germany, Austria and Switzerland).
You may also be required to supervise other regulatory affairs individuals depending on business need.
You will have a broad range of Regulatory Affairs issues gained within the CRO or Pharmaceutical industry. Extensive knowledge of relevant regulatory applications and procedures, especially those related to clinical trials in the relevant countries, along with proven success in agency influencing and negotiation, would be an advantage.
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