Manager Program Coordination(
Vacaturenummer:
00000TC4)
Omschrijving
Crucell is a global biotech company that focuses on the development, production and marketing of vaccines and antibodies to prevent and combat infectious diseases.
Within Crucell talented, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Crucell.
For our department we are currently seeking for a fulltime
Manager, Program Coordination (m/f)
Department:
Project Management Organization
Job Description:
The Manager, Program Coordination (PC) provides coordination support to the Clinical functional teams as assigned to ensure completion of deliverables that are balanced for quality, timeliness and resources. The Project Coordinator assists the Program Manager in providing planning and resource management support to the Compound Development Teams (CDTs).
In this role, the PC facilitates team communications by maintaining and tracking cross-functional timelines, deliverables, and milestones including cross-project dependencies. Ensure project schedules, resources and underlying assumptions are integrated and aligned across functions. Next to this the PC facilitates critical path analysis and optimization planning. The PC will assist teams in determining schedule and resource requirements and conduct contingency planning/scenario analyses to modify schedule to keep project on track and tracks team performance metrics. Communication with the teams is a key aspect of this role. The PC utilizes scheduling, resource management tools, provides coordination expertise and maintains cross-disciplinary process and project knowledge.
Primary duties:
- The Program Coordinator (PC) provides and maintains cross-functional project plans, team reports, and resource management support to ensure the completion of deliverables balanced for quality and timeliness.
- Assists the Program Manager in providing and maintaining system tools and Cross-functional project plans aligned across R&D (Clinical, Pre-clinical, CDO’s, CPS, Biomarker, and PDMS) to support the Compound Development Teams (CDTs).
- Is a core member of the Project Management Team (PMT/OPT).
- Assist the Clinical Program Manager (CPM) in providing Clinical Cross-functional project plans aligned across the clinical functions (Clinical pharmacology -small molecule only, R&D Ops support, Reg/QA, & QC) to support the Clinical Teams (CTs).
- Facilitates critical path analysis, contingency planning/scenario analyses and proposes strategies and solutions to modify schedule to keep project on track in collaboration with the CPM & PM.
- Generates program reports and communications to ensure team and program alignment of deliverable expectations.
- Provides overall support to the Clinical functional representatives to ensure completion of deliverables that are balanced for quality, timeliness and resources. Facilitates project communications by maintaining and tracking timelines, deliverables, and milestones.
- Conducts contingency planning/scenario analyses and proposes strategies and solutions to modify schedule to keep project on track.
- Provide regular reports and analysis on resource demand and supply.
- Facilitate regular review of workload and resource analyses, including business plan.
Kwalificaties
Qualifications:
Education
- At least BSc and equivalent work experience required. Advanced degree preferred.
Experience
- 5 years industry experience with at least 3 years in Drug Development and a detailed knowledge of the Drug Development process.
- Detailed knowledge of: project planning, tracking, resource management, project planning and scheduling tools, and cross-project analyses.
Competencies:
- Understanding of clinical development/trial execution required
- Knowledge of project planning, tracking, resource management
- Delivery of results
- Project management
- Customer focus
- Innovation
- Communication
- Adaptability
- Analytical skills
What’s in it for you…?
“Caring for the world, one person at a time…”
As an employee we consider you as our most valuable asset. We take your career seriously.
As part of a global team in an innovative environment your development is key and our day-to-day responsibility.
Through e-university, on the job training, various projects and programs, we ensure your personal growth.
Our benefits make sure we care for you and your family now and in the future.
Will you be our new colleague? Please apply online.
Primaire locatie: Europa/Midden-Oosten/Afrika-Nederland-Zuid Holland-Leiden
Organisatie: Crucell Holland BV (7328)
Functie: Clinical Trial Coordination
Vacaturenummer:
00000TC4)
Omschrijving
Crucell is a global biotech company that focuses on the development, production and marketing of vaccines and antibodies to prevent and combat infectious diseases.
Within Crucell talented, entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Crucell.
For our department we are currently seeking for a fulltime
Manager, Program Coordination (m/f)
Department:
Project Management Organization
Job Description:
The Manager, Program Coordination (PC) provides coordination support to the Clinical functional teams as assigned to ensure completion of deliverables that are balanced for quality, timeliness and resources. The Project Coordinator assists the Program Manager in providing planning and resource management support to the Compound Development Teams (CDTs).
In this role, the PC facilitates team communications by maintaining and tracking cross-functional timelines, deliverables, and milestones including cross-project dependencies. Ensure project schedules, resources and underlying assumptions are integrated and aligned across functions. Next to this the PC facilitates critical path analysis and optimization planning. The PC will assist teams in determining schedule and resource requirements and conduct contingency planning/scenario analyses to modify schedule to keep project on track and tracks team performance metrics. Communication with the teams is a key aspect of this role. The PC utilizes scheduling, resource management tools, provides coordination expertise and maintains cross-disciplinary process and project knowledge.
Primary duties:
- The Program Coordinator (PC) provides and maintains cross-functional project plans, team reports, and resource management support to ensure the completion of deliverables balanced for quality and timeliness.
- Assists the Program Manager in providing and maintaining system tools and Cross-functional project plans aligned across R&D (Clinical, Pre-clinical, CDO’s, CPS, Biomarker, and PDMS) to support the Compound Development Teams (CDTs).
- Is a core member of the Project Management Team (PMT/OPT).
- Assist the Clinical Program Manager (CPM) in providing Clinical Cross-functional project plans aligned across the clinical functions (Clinical pharmacology -small molecule only, R&D Ops support, Reg/QA, & QC) to support the Clinical Teams (CTs).
- Facilitates critical path analysis, contingency planning/scenario analyses and proposes strategies and solutions to modify schedule to keep project on track in collaboration with the CPM & PM.
- Generates program reports and communications to ensure team and program alignment of deliverable expectations.
- Provides overall support to the Clinical functional representatives to ensure completion of deliverables that are balanced for quality, timeliness and resources. Facilitates project communications by maintaining and tracking timelines, deliverables, and milestones.
- Conducts contingency planning/scenario analyses and proposes strategies and solutions to modify schedule to keep project on track.
- Provide regular reports and analysis on resource demand and supply.
- Facilitate regular review of workload and resource analyses, including business plan.
Kwalificaties
Qualifications:
Education
- At least BSc and equivalent work experience required. Advanced degree preferred.
Experience
- 5 years industry experience with at least 3 years in Drug Development and a detailed knowledge of the Drug Development process.
- Detailed knowledge of: project planning, tracking, resource management, project planning and scheduling tools, and cross-project analyses.
Competencies:
- Understanding of clinical development/trial execution required
- Knowledge of project planning, tracking, resource management
- Delivery of results
- Project management
- Customer focus
- Innovation
- Communication
- Adaptability
- Analytical skills
What’s in it for you…?
“Caring for the world, one person at a time…”
As an employee we consider you as our most valuable asset. We take your career seriously.
As part of a global team in an innovative environment your development is key and our day-to-day responsibility.
Through e-university, on the job training, various projects and programs, we ensure your personal growth.
Our benefits make sure we care for you and your family now and in the future.
Will you be our new colleague? Please apply online.
Primaire locatie: Europa/Midden-Oosten/Afrika-Nederland-Zuid Holland-Leiden
Organisatie: Crucell Holland BV (7328)
Functie: Clinical Trial Coordination