What we offer
Joining our consulting team in Belgium means giving your career a step forward. Thanks to the privileged partnership we have with our well-established clients, leaders in their domain, we offer our consultants unique projects to develop their skills, and put their professional experience in the pharma industry on the fast track.
As an expert on the client side, you can count on us to support you at each step of your project thanks to regular touch points with our Key Account Manager. We then also carefully choose with you what would be your next assignment that is matching your career goal whether it is in Consulting or in one of our Functional Services Platforms.
We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.
Job Description
Keyrus Life Science is looking for a Value Evidence consultant to join our consulting team for a client project based in Wavre.
Main responsibilities:
The mission of the Value Evidence Consultant in the Vaccines department is a global role supporting the team members for specific tasks as well as potentially leading the implementation of targeted projects.
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This would include collaborating with the regional and local operating
countries (LOCs) to understand the needs in countries for reimbursement of a vaccine, accordingly, guide the evidence generation, project management and publishing the results as appropriate. - Coordinate with countries, global and regional matrix team stakeholders to implement the asset-specific value evidence plan.
- Review of the cost-effectiveness model inputs for base-case and sensitivity analysis, specific slide deck formulation for regional/country support materials and
organization of potential webinars, trainings accordingly on specific topics.
Your primary tasks :
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Implement selected value evidence plan activities
- Project Management of value evidence activities
o Obtain internal approvals as per the internal process
o Project contracting
o Reviewing interim results and reports
o Reviewing final report and associated slide deck as needed;
o Development of publication/poster potentially in collaboration with Key External
Experts
- Collaborate with regional value evidence teams and global cross-functional teams to plan and coordinate evidence generation activities in accordance with priority setting
- Understand the needs and pathway in countries towards reimbursement of vaccine
- Management or development of other supporting materials (Toolkits, Slidedecks, Reports, Access Dossiers, etc),
- Support cost-effectiveness model adaptation by collecting, reviewing, and communicating data inputs with global, Regional, LOC colleagues
Your profile:
- At least 5 years of experience in the field,
- experience in evidence generation activities (literature review, preference elicitation studies, comparative analysis, modelling)
- Language skills: French and English
Who we are
Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.
At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skilfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.
