Associate Director - Project Management - FSP - Drug Development exp
New Yesterday
Social network you want to login/join with:
Associate Director - Project Management - FSP - Drug Development exp, London
col-narrow-left
Client:
Location:
London, United Kingdom
Job Category:
Other
-
EU work permit required:
Yes
col-narrow-right
Job Reference:
640675c3a090
Job Views:
7
Posted:
18.07.2025
Expiry Date:
01.09.2025
col-wide
Job Description:
Job Title: Associate Director - Project Management - FSP - Drug Development exp
Job Location: Great Britain, United Kingdom
Job Location Type: Remote
Job Contract Type: Full-time
Job Seniority Level:
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
The PPD FSP Solution:
PPD's Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.
Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.
Discover Impactful Work:
The Associate Director within Drug Development will oversee high-level plans and progress for asset development, from pre-clinical stages to commercial launch. This role involves close collaboration with various stakeholders to ensure timely availability of documents and alignment with corporate strategy. Act as primary point of contact when concerning integrated cross-functional project planning and status. They closely collaborate with stakeholders who own, contribute to, and/or manage the project and the impact of decisions and changing circumstances. This to drive timely availability of documents as planned.
A day in the Life:
Project Lead responsibilities:
- Serves as the primary contact between the sponsor and the organization at the project level.
- On projects where the scope requires, ensures clear delineation in responsibilities and communication pathways for secondary project leads (such as lead in a specific region, lead for a specific vendor(s) or subset of delivery).
- Drives and owns the overall delivery of the cross-functional project (time, cost, quality).
- Ensures financial stewardship at a project level by demonstrating an intimate understanding of the contract, resource alignment to budget, management of Out of Scope activity, drive the Con Mod process/negotiations and team execution to timelines.
- Establishes, communicates and manages customer expectations to achieve optimal delivery during the project.
- Drives Risk Identification and Issue Resolution at project level (RBQM/RESOLVE).
- Ensures project team compliance with organization policies, SOPs, ICH- GCP, regulatory and project specific requirements
- Accountable for strategic indication or client-specific portfolio management within a Therapeutic Unit.
- Expertly navigates the need to dive in/dive out of situations while ensuring the Project Lead remains empowered .
- Provokes critical thinking in Project Lead related to execution of delivery, financial negotiations and prioritization.
- Provides insight into proposal strategy in prep for bid defense.
- Works with Therapeutic Unit Head in development of business growth strategies.
- Maintains awareness and engages as appropriate in the Con Mod process.
- Communicates with People Manager(s) to support the development of the employee providing expertise and perspective related to client needs, indication and therapeutic knowledge.
- Accountable for the career development and performance management of a group of project delivery direct reports in line with The Core People Manager Expectations at the organization.
- Partners with project team leadership and key stakeholders (i.e OD, SLT, BPL, DevOps, functional leadership) to ensure areas of development, training needs and coaching are aligned through routine and active engagement.
- Provides coaching, soft skill and technical skill development to grow our Project Delivery talent.
- Provides support/direction to direct report(s) with regards to knowledge of organization systems, processes and tools within Project Delivery.
- Liaises with Resourcing Leads, TU Leadership and other key stakeholders to advocate for direct report(s), ensuring appropriate project assignment(s) and balance between career development and business needs.
- Fosters collaboration and connections amongst peers.
- Cultivates high quality relationships with each direct report to create a trusting environment.
- Participates in Initiatives to foster talent development.
- Advanced degree (Master or PhD) in a health-related discipline or equivalent experience.
- At least 10 years of drug development experience across different disease areas.
- At least 5 years of program management experience in the pharmaceutical or biotech industry.
- Strong leadership, communication, and collaborative skills.
- Proven ability to mediate conflict and manage change.
- Advanced project management skills and experience with MS Project.
- PMP certification is an advantage.
- Fluent in English (verbal and written).
- Experience in Regulatory Affairs and/or Clinical Development is a plus.
- Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
- Able to work upright and stationary for typical working hours.
- Ability to use and learn standard office equipment and technology with proficiency.
- May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments.
- Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
- May require travel. (Recruiter will provide more details.)
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Accessibility/Disability Access
Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.
This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
This job is curated by Lifelancer.
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
#J-18808-Ljbffr- Location:
- London, England, United Kingdom
- Salary:
- £150,000 - £200,000
- Job Type:
- FullTime
- Category:
- Management & Operations