Senior Project Manager (French Speaking)

Wepclinical

Chiswick

On-site

GBP 45,000 - 75,000

Full time

14 days+
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Benefits offered by this job

Group Private Medical Insurance
Group General Life Assurance
Group Critical Illness and GroupIncome

Job summary

WEP Clinical in the United Kingdom is seeking a Senior Project Manager to lead the setup, implementation, and management of Post Approval Named Patient Programs (PA-NPP) and related projects.

You will oversee regional and global PA-NPP projects, ensure timelines and budgets align with the SOW, and lead the project team to deliver high-quality outcomes.

Qualifications

  • Bachelor's degree in health or science field required.
  • Fluency in French is required for this role.
  • Significant experience in project management or clinical research with PA-NPP exposure.
  • Experience with eTMF and CTMS systems.
  • Ability to handle confidential information with discretion.

Responsibilities

  • Lead and oversee regional and global PA-NPP or related projects.
  • Manage project timelines and budgets per contract and SOW.
  • Provide leadership, training, and oversight of project teams.

Skills

Team Player
Adaptable
Detail Oriented
Problem Solver
Fluency in French
Communication skills

Education

Bachelor's Degree in health or science field

Tools

Microsoft Office
eTMF
CTMS

Job description

Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organization dedicated to advancing clinical research and transforming lives.

Role Objectives:

The WEP Clinical Senior Project Manager is responsible for leading and overseeing the setup, implementation, and management of Post Approval Named Patient Programs (PA-NPP) and/or related projects.

  • Team Player
  • Adaptable
  • Detail Oriented
  • Problem Solver

Lead and/or oversee regional and global PA-NPP or related projects, ensuring project timelines are met as per contract.

Ensure all program project plans, including timelines and budgets, are developed, maintained, and in compliance with the Scope of Work (SOW).

Responsible for the project team's leadership, training, and operational oversight, including overseeing delegation of support staff activities as necessary; may serve as line manager of direct report(s) in some instances.

Build and maintain positive client relationships, communicating with clients to ensure WEP Clinical operational processes are maintained and projects are delivered within scope.

Identify, evaluate, monitor, and mitigate any factors or processes that may threaten project quality (risk management), and communicate identified risks to internal team members, upper-level management, and clients as appropriate.

Develop, identify, define, and document study-specific training requirements to assure project-level compliance across projects.

Prepare and finalize Out of Scopes (OOS), ensuring Project Teams identify OOS effectively and develop effective change orders in collaboration with WEP Clinical Business Development.

Assure project teams are managing programs in accordance with WEP Clinical SOPs and Policies.

Participate in proposal meetings for potential clients.

Review documentation for the Electronic Trial Master File required for Programs, including treatment guidelines or protocols, case report forms and completion guidelines, informed consent documents, investigator agreements, investigator brochures, logic checks, data handling guidelines, and all other documents as required by the client.

In conjunction with management, assist with developing, documenting, and updating internal WEP Clinical procedures and processes required for consistency across programs, such as SOPs, working practices, and related quality assurance forms.

Provide operational oversight during Programs and projects, including reviewing site visit preparation documents, site visit reports, and site payments; audit the compilation and completion of the eTMF and CTMS; and maintain current knowledge of FDA, GDPR, and other global regulations and GCP/ICH Guidelines for Post-Approval Named Patient Programs and Clinical Research.

Fluency in French is a requirement for this role

Bachelor's Degree (in a health or science field preferred)

Significant experience and demonstrated ability in project management or clinical research, with direct clinical trial or PA-NPP experience in a CRO or research-related organization

Computer literacy and proficiency in Microsoft Office, as well as experience with an eTMF and CTMS, and an understanding of basic data processing functions, including electronic data capture

Ability to handle confidential information with complete discretion

Strong organizational, interpersonal, and attention-to-detail skills, with the ability to manage multiple priorities and interact with all levels of staff to coordinate and execute study activities

Effective verbal and written communication skills, including the ability to express complex ideas

Knowledge of the clinical development process from Phase I through regulatory submission, and working knowledge of current ICH GCP guidelines

Ability to reason independently to assess and recommend specific solutions in clinical settings, and to set baseline targets, track trends, and implement mitigation plans

What We Offer:
  • Group Private Medical Insurance
  • Group General Life Assurance
  • Group Critical Illness and Group Income Protection
  • Salary sacrifice pension scheme
  • Enhanced maternity & paternity pay
  • Educational Assistance allowance
  • Paid volunteering day
What Sets Us Apart:

WEP Clinical partners with biopharmaceutical Sponsors to help them bring treatments closer to the patients who need them most. Through end-to-end clinical trial delivery, home health services, expanded access programs, and market access consultancy, we provide flexible, fit-for-purpose solutions that support drug development, improve access, and help therapies reach the right patients at the right time. With more than 15 years of global experience, we have supported programs across 150+ countries, combining operational scale with the agility and personalised service of a specialised provider. Our work helps bridge critical gaps in care, ensuring safe, ethical, and efficient access to promising new treatments.

We're Committed to Our Team:

WEP has many initiatives to encourage wellness, growth, development, and team relationships. Check out our LinkedIn life page to learn more about our team events and all that we do to support our employees.

How We Work at WEP Clinical:

At WEP Clinical, we look for individuals who are conscientious, exercise sound judgement, and engage with others thoughtfully and professionally. We believe excellence is achieved through integrity, accountability, and respect for diverse perspectives – and we are committed to helping our people grow and succeed in an inclusive, supportive environment.

Our Services Include:
  • Access Programs
  • Clinical Trial Services
  • Patient Site Solutions
  • Clinical Trial Supply
  • Market Access and Commercialization
Data Privacy Notice:

WEP Clinical is committed to protecting your personal information throughout the recruitment process. By applying, you acknowledge that your personal data will be processed in accordance with our Privacy Policy and Job Applicant Privacy Notice.

Privacy Policy: https://www.wepclinical.com/privacy-policy/

Job Applicant Privacy Notice: https://www.wepclinical.com/Job-Applicant-Privacy-Notice/

Equal Opportunity Statement:

WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.

WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.

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