Global Feasibility Lead

3 months ago

High Wycombe, United Kingdom Johnson & Johnson Full time

**Global Feasibility Lead**:
**Location: High Wycombe, UK, or Turnhout, Belgium (Hybrid)**:
At Johnson & Johnson Innovative Medicine, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and sophisticated diseases of our time.

We have an exciting opportunity for a **Global Feasibility Lead **(GFL) located within commutable distance of High Wycombe, UK or Turnhout, Belgium to hold primary accountability for the delivery of program and study-level clinical trial feasibility. This role encompasses R&D trials across early development, late development, and phase 3b / IV interventional trials. You will lead and facilitate the global feasibility process end-to-end within one or more therapeutic areas (TA), serving as the primary liaison with study team stakeholders at central, regional, and country levels for both in-house and outsourced trials. Success in this position involves delivering feasibility activities—strategy, plans, activities, timelines, synthesis of insights, and presentations to study teams—within timelines and with high quality, supporting operational planning and decisions for predictable delivery.
- Are you interested to join our team? Please read further _

**Principal Responsibilities**:

- Lead feasibility activities across functions, collaborating closely with GPL to design and present recommendations to study team leads within defined timelines.
- Partner with study team members, country teams, and the feasibility insights and data analytics team to design and conduct global feasibility activities on time with high-quality delivery.
- Provide updates on feasibility process to study and program team stakeholders, including escalation of key issues, risks, and recommended solutions.
- Ensure country points of contact (POCs) have relevant clinical development plan information and provide strategic direction for study feasibility to facilitate local insights creation.
- Support early clinical operations roles by providing initial enrollment timelines, budget plans, and patient recruitment strategies.
- Effectively communicate feasibility insights to influence protocol development, study timelines, and country/site selection.
- Ensure consistent standards are applied across projects and support continuous improvement activities.
- Collaborate with Feasibility Group Lead to develop and implement TA-aligned strategies for feasibility insights generation.
- Implement country engagement strategy aligned with the clinical development plan and trial program footprint.
- Analyze data and insights to develop global understanding of feasibility outputs and present recommendations to study teams.
- Maintain continuity and document changes throughout feasibility process stages.
- Set trial baseline commitments for site initiation and recruitment expectations, ensuring agreement at global and TA levels.
- Facilitate study baseline commitment change process at country and study levels.
- Support clinical operation roles in effective scenario generation and planning.
- Assist in the development of systems, processes, and work practices for assessing program and protocol feasibility.
- Provide early feasibility information leveraging existing data sources and organizational knowledge.

**Principal Relationships**:
Contacts inside the company may include: Global Program Lead (GPLs), GOHs, GTLs, GCO Country Managers/Heads, Clinical Research Manager (CRM)/Functional Manager (FM), Local Trial Manager (LTM), Site Manager (SM), Feasibility Staff, IPE staff, Therapeutic Area functions and Clinical Team members, medical affairs teams Contacts outside the company may include: Investigational Sites, Key Opinion Leader (KOLs), Advisory Board Members, Patient Engagement Groups, Academic Centers, vendors with focus on study placement, recruitment & retention capabilities.

**Qualifications**:
**Education and Experience Requirements**:

- 6+ years’ experience in Clinical Operations OR other relevant experience -such as data analytics.
- Specific oncology therapeutic area experience is advantageous, but not essential
- Minimum of degree-level qualification is required
- Minimum 3 years' feasibility experience required
- A broad-based experience clinical research, including clinical trial conduct, knowledge of GCP and a good understanding of the processes associated with study / site feasibility, study/project management, monitoring, clinical and regulatory operations
- Experience of leading multinational clinical trials is preferred
- Experience in assessing Patient Recruitment Needs and building patient recruitment strategies for programs is highly desired
- Ability to strongly leverage, interpret, explain, represent, and drive unbiased data insights into clinical trials operational planning
- Ability to develop deep insights, uncover unmet needs, drive innovation, inspire, develop, collaborate and lead within a global matrixed te

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