Overview
As a RWE expert you will contribute to the design and execution of studies to generate real-world insights (RWI) and real-world evidence (RWE) to inform strategic internal decision-making, thereby empowering differentiated R&D activities within our clients position. You will also support external decision-making by interacting with key stakeholder groups such as patients, regulators, policy makers, payers, and prescribers, and contribute to the wider epidemiological and medical understanding of specific diseases. Driven by business needs, you will help conceptualize RWE projects to meet business requirements and support the Global RWE strategy and execute the tactical plan.
Key Responsibilities
* Support the Global RWE Strategy: Provide input to help drive the Global RWE strategy & tactical plan based on request from the strategy lead responsible for the respective patient population.
* Support RWE Study Design & Execution: Assist in planning and execution, including protocol development, and analysis specifications following best methodological standards. Use internal and external real world data to generate disease insights and epidemiological information to support business needs.
* Innovate Study Designs: Drive innovative study designs, including identifying new data sources and applying advanced analytics (e.g. causal inference, machine learning).
* Collaborate with External Partners: Work with RWE contractors and external vendors on RWE projects.
* Clarify Protocol Implementation: Provide RWE analysts with clarifications concerning protocol implementation.
* Interpret Analysis: Drive interpretation of analysis in collaboration with the RWE strategy lead and internal stakeholders and communicate analysis interpretation internally and externally.
* Ensure Alignment: Support the RWE strategy lead to ensure alignment of RWE tactics with the overall program strategy and clinical development plan
Key Competencies
* Ph.D. or Master's degree in relevant areas (e.g. epidemiology, pharmacy, biostatistics, data science, public heath).
* Hands-on experience in successfully conceptualizing and delivering prospective or retrospective observational studies in academia, consulting or pharmaceutical companies, preferably related to disciplines of pharmaco-epidemiology, population health sciences or health services research
* Experienced in causal inference methodologies, including but not limited to target trial emulation, propensity score methods, instrumental variable analysis, interrupted time series analysis etc.
* Knowledge of clinical development, especially Ph1 and Ph2 clinical trials.
* Drive for innovation and creativity. Be open-minded, science-driven and adapt to new ways of working
* Passionate to leverage data to generate insights and enable data-driven decision
* making.
* Experience communicating advanced analyses to non-technical audiences.
* Ability to influence stakeholders without authority
* Ability to develop and maintain strong collaborative relationships with key partners and stakeholders based on in-depth understanding of stakeholder needs and strategic focus
* Adeptness in using his/her relationships with internal and external stakeholder groups to provide strategic input through synthesized thinking, building advocacy and empowering implementation of the solutions in support of creating patient value and our clients portfolio performance
ABOUT PLANET PHARMA
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
www.planet-pharma.com
TO APPLY
Please click ‘apply’ or contact Hamish Hopkins R3 at Planet Pharma for more information:
E:
T: : +44 20 3953 1459