Senior Value Evidence Analyst

What we offer

You will play an important role in Patient Reported Outcomes assessments (PRO) and Clinical Outcomes Assessment (COA) in the drug development processes. This mission aims to demonstrate the burden of disease on patients and the value of vaccines in both preventing disease and reducing disease severity in breakthrough disease, thereby maintaining overall quality of life of vaccine recipients.

Joining our consulting team 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 trainingour 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

This role entails to plan the evidence generation to support the value of the vaccines in Research and Early Development, contributing in the generation of cross functional Value Evidences Plans integrating Health Economics, Outcomes Research, PRO/COA, Real World Data stakeholder activities.

Under direction of PRO manager, you will be responsible to:

• Coordinate and lead the development of literature review to inform the COA strategy, identifiying the potential concepts of interest and the COA tools applicable to measure those.
• Coordinate and lead the development of COA/PRO specific studies to generate evidence of the fit-for-purpose of the tools implemented in the COA/PRO strategy.
• Support the appropiate implementation of PROs in clinical trials.
• Interact with statistical teams for appropriate analyzis, study reports and publications and collaborate with regulatory agencies.
• Prepare abstracts and manuscripts presenting PRO results from clinical development, PRO development and validation studies.
• Develop and provide training on COA-related topics to other departments.

Profile

• Master’s degree in Psychology, Psychometrics, Social Sciences, Outcomes Research, Health Services Research or a closely related discipline.
• Minimum 5 years’ experience in pharmaceuticals, particularly in drug development, so as to understand drug development process, with demonstrated experience in clinical trial planning and execution.
• Experience with PRO/COA requirements for regulatory and with Health Technology Assessement/reimbursement agencies.
• Strong communication skills, with stakeholder engagement with Clinical, Health Outcomes and Regulatory.
• ICT Skills (software, operating systems, hardware, etc.)
• English Fluent.

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 skillfully, 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.