Clinical Project Manager
CCBR-SYNARC is the world’s leading pharmaceutical service organization dedicated exclusively to global clinical trials. CCBR-SYNARC medical image-analysis, subject-recruitment, and biochemical-marker services enable life-science industry clients to execute clinical trials accurately while decreasing the time, uncertainty, and cost of product development. CCBR-SYNARC has contributed to the approval of more leading compounds, across a broad spectrum of therapeutic areas, than any other central imaging provider.
CCBR-SYNARC is looking for a special person to be a Clinical Project Manager in Hamburg, Germany to lead centralized imaging services for clinical trials.
Summary of Position:
The Clinical Project Manager coordinates efforts across SYNARC offices and departments to achieve on-time delivery of radiology services to the sponsor. The Clinical Project Manager provides a central point of communication for the SYNARC study team and senior management and for the sponsor to ensure that all deliverables are accurate, meet internal standards, and fulfill contractual obligations.
Responsibilities:
- Manages all communications with the Sponsor regarding timelines and study specific deliverables.
- Facilitates regular meetings with the Sponsor study team.
- Develops and maintains project plans that encompass all contracted deliverables.
- Tracks study progress and escalates issues that require resolution.
- Leads the SYNARC study team, which includes representatives from all functions, to support the study.
- Coordinates the development of study specific procedures.
- Provides regular internal status updates to the study team and senior management.
- Reviews and submits work performed; validates monthly invoices.
- Identifies need for change orders and works with the Account Executive to obtain Sponsor approval.
- Prepares financial and activity forecasts for capacity planning.
- Participates in and/or leads initiatives to improve processes.
Profile
- Advanced scientific degree, or directly-relevant equivalent experience.
- 2 or more years of late stage drug or medical device development,
- 2 or more years of project management
- Demonstrated ability to effectively communicate to external sponsors and internal cross-functional study teams.
- Demonstrated ability to multitask and set priorities.
- Strong time management and organizational skills.
- Strong written and oral communication skills.
- Ability to manage and mobilize a study team that does not report directly to you.
- Ability to make quick decisions, solve problems, and adapt to changing environments and requirements.
- Ability to set and manage project budgets.
- Proficiency with MS Office, and experience with MS Project or other project management software.
- Working knowledge of relevant imaging modalities.
We offer
We offer an interesting, varied and creative job with significant people interaction in a global and scientific setting. We provide service with a high scientific content in support of the development of new important medications to society. You will be playing an important part, interacting with clinical sites and pharmaceutical companies worldwide.
We are a young, innovative, company and our service and scientific skills are a competitive edge. We offer you the opportunity to grow as an individual together with the company.
Contact
For further information, please contact CCBR-SYNARC at +49 40 25 332 50
If you are interested in this position and would like to apply, please send your application in English per email to: annette.pielecka@synarc.com.
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