Senior Project Manager
il y a 3 semaines
Description:
- Location: Beerse, Belgium - Office
- Schedule: Full-time, permanent
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it is the best of both worlds.
- TalentSource Life Sciences (the sponsor-dedicated division of CROMSOURCE), is searching for a Senior Project Manager to join one of our clients, one of the most innovative pharmaceutical companies in the world.
The Project Manager should have prior project management experience in a clinical setting, ideallyMain Job Tasks and Responsibilities:
- Defining the overall project strategy for year 3 of the project together with the project
coordinators and WP leaders and assure the strategic goals are reflected in the project
management plan and all actions to accomplish this plan (including facilitating steering committee
and cross-WP meetings).
- Ensuring timely and accurate documentation and communication of progress and issue
escalation. Day-to-day monitoring of the project management plan and maki
adjustments as needed, in close alignment with the work package leaders and the project
2 coordinators. Leading activities of the ongoing review of progress on deliverables, completion of
milestones and risk analysis and mitigation.
- Monitoring project budget and supervising actuals vs forecast expenses and reviewing
assigned vendor invoices/spend.
- Managing the identified KPIs to measure outcomes and success for the project,
ensuring all partners are aligned on the approach to reach these KPIs. Monitoring risk and
mitigation planning which may lead to deviation of certain KPIs.
- Providing leadership and project management for the emerging sustainability initiatives
which must create mid and long-term value for each of the consortium partners. Support
the consortium in identifying these most appropriate sustainability projects and helping to
build the Return-on-Investment case and business plan for the sustainability phase.
- Leading the communication, including supporting internal and external dissemination
activities to ensure value generation for all consortium partners.
- Successful project closeout, assuring all administrative and financial requirements are
fulfilled and making the project and its deliverables audit ready
Education and Experience:
- An advanced biomedical sciences degree is preferred (Master's/PhD/PharmD degree) with a minimum of 10 or more years of total business experience required.
- A minimum of 6 years of project management experience in global clinical research either in a
CRO, Pharma, consultancy or other clinical trial sponsor environment is preferred.
- Proven experience in managing and executing complex projects from start to finish.
- Excellent organizational, project management, and influential management skills, complemented
by a "hands-on" operational and business planning orientation is required. PMI (or equivalent)
certified.
- Experience leading public-private partnerships/consortium projects.
- Familiarity with and interest in health technology and health information technologies is
required; direct experience with health information technology, healthcare technology, and
- Experience with real-world evidence and data sciences is preferred.
- Experience contributing to innovative analytical solutions is preferred.
- Experience with management and supervision of vendors is preferred.
- A self-starter with a strong results orientation, who can operate independently and can navigate
complex, matrixed environments are required.
Specific Role Requirements and Skills:
- Outstanding communications skills, both written and oral, capable of effectively summarize
abstract concepts into clear, concise, and insightful business cases.
- Experience collaborating successfully with global clinical teams, R&D Operations, Therapeutic
Areas and Medical Affairs are preferred.
- Strong team player, motivating professional colleagues and stakeholders cross-functionally and
across organizations within the consortium.
- Fluent in Dutch and English, must be based in Belgium
Our Benefits of Working for TalentSource in Belgium:
- Competitive Salary
- Group and hospitalisation insurance
- Electronic meal vouchers
- Internet reimbursement
- Dedicated Line Manager
- Regular face-to-face or phone meetings with the line manager
- Full annual performance review process
- Ad-hoc team events and end-of-year party
- Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally
- Employee satisfaction survey - your feedback is important for continuous improvement
The Application Process
Who will you be working for?
About CROMSOURCE
- CROMSOURCE is a family-owned international, full-service Contract Research Organisation that, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The su
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