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.
$ads={1}
Job Description
Are you looking for a high-profile health outcomes role that shapes evidence generation for our vaccines across the region? If so, this Director, Value Evidence & Outcomes (VEO) role could be an exciting opportunity to explore.
As a Regional VEO Director, you will be responsible to develop and implement local epidemiology and health outcomes evidence strategies/plans for GSK vaccines, to support vaccination recommendations and reimbursement pre/post-launch and throughout the vaccine life cycle in Europe.
This role will provide YOU the opportunity to lead key activities with high impact to the business that can help progress YOUR career.
These responsibilities include some of the following:
- Develop, assess, and lead evidence generation plans and activities to address access needs of the Local Operating Companies (LOC).
- Ensures robust study designs are in place to address local needs in accordance with GSK SOPs; develop dissemination plans & leverage data for payer discussions
- Lead customer engagement on public health priorities to shape vaccine evaluations.
- Lead scientific discussion PIs in collaborative research studies
- Lead the validation of local value proposition, value dossiers and, transition to payers.
- Create, with allied functions, mid/long term enterprise-wide scientific collaboration with stakeholders to ensure impact on performance.
- Build effective relationships with key strategic suppliers(s) at executive and operational levels.
- Timely development and delivery of epidemiology, health outcomes and health economic evaluations, or other appropriate tools to support vaccines value assessment.
- Lead broad-based, cross-portfolio scientific affairs discussions with governments, institutions, and Healthcare Organizations (HCOs) in the LOC.
- Develop science/public health policy activities with stakeholders e.g. white papers, incorporation of evidence into guidelines, etc.
Profile
- Masters or Post graduate degree in Public Health, Epidemiology, HEOR, Health Policy or related field
- Experience in value access, health policy or allied functions
- Experience in advising/implementation of Public Health programs
- Expertise developing scientific collaboration with external stakeholders
- Supplier relationship management experience at operational and strategic level.
- Pharmaceutical experience that includes exposure to study design, medicine development and the reimbursement process.
- Experience managing a globally matrixed team.
- PhD
- Excellent communication, presentation and listening skills
- Ability to see solutions to complex, unique situations where Scientific Engagement principles can be applied
- Operates effectively in multicultural matrix organisation and networks readily
Basic Qualifications:
Preferred Qualifications:
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.