Company
SeniorReal-WorldEvidenceScientist
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“Senior Real-World Evidence Scientist. Skills: RWE projects, Observational studies, Data interpretation, Scientific communication. Execute RWE projects. Co-lead RWE projects”
What You'll Achieve.
Generate high-quality scientific insights; Support clinical development; Deliver timely, decision-relevant evidence; Ensure scientific validity; Ensure fitness for purpose; Deliver evidence that informs decision-making; Strengthen scientific consistency; Strengthen RWE capability
Industry & Context.
Insight generation
What They're Looking For.
Must Have
Master's degree or equivalent, 5+ years of relevant experience in RWE, observational research, or related scientific roles, Understanding of observational study design, Understanding of secondary data research, Knowledge of common RWE methodologies, Knowledge of study biases, Knowledge of confounding, Knowledge of endpoint definition, Principles of causal inference, Ability to translate complex clinical and data findings into meaningful scientific insights, Communication skills, Collaboration skills, Ability to work effectively in cross-functional and matrixed teams, Ability to communicate clearly with technical and non-technical stakeholders, Ability to manage interactions with external collaborators or vendors, Ability to plan and prioritize work with growing autonomy, Attention to scientific quality, Attention to operational detail
Nice to Have
PhD degree, Experience supporting evidence generation in one or more non-oncology therapeutic areas, Experience in cardiovascular therapeutic areas, Experience in renal and metabolism therapeutic areas, Experience in respiratory & immunology therapeutic areas, Experience in rare disease therapeutic areas, Experience in contributing to publications, Experience in scientific communications
What You'll Do.
Generate scientific insights
Support clinical development
Contribute to end-to-end delivery
Apply scientific expertise
Apply technical expertise
Design observational studies
Analyze observational studies
Interpret observational studies
Communicate observational research
Collaborate with cross-functional colleagues
Collaborate with external partners
Collaborate with vendors
Deliver decision-relevant evidence
Serve as subject matter expert
Design complex observational studies
Contribute to study concepts
Contribute to protocols
Contribute to statistical analysis plans
Contribute to analysis specifications
Ensure scientific validity
Ensure fitness for purpose
Translate findings into insights
Partner with internal stakeholders
Oversight of timelines
Oversight of deliverables
Prepare scientific materials
Deliver scientific materials
Contribute to methodological discussions
Contribute to best practices
Contribute to team knowledge-sharing
How You'll Work.
Team & Collaboration
Collaborate with cross-functional colleagues; Collaborate with external partners; Collaborate with vendors; Partner effectively with internal stakeholders; Work effectively in cross-functional and matrixed teams; Communicate clearly with technical and non-technical stakeholders; Manage interactions with external collaborators or vendors
Communication Scope
Communication skills; Communication of evidence; Communication of knowledge; Communicate clearly with technical and non-technical stakeholders
Process & Methodology
Project execution, Co-leadership, Study delivery, Manage selected workstreams, Oversight of timelines, Oversight of deliverables, Oversight of quality, Plan and prioritize work
Full Job Description
**Job Description:** We are seeking a highly skilled and motivated _Senior Real-World Evidence (RWE) Scientist_ who will be responsible for executing and co-leading RWE projects that generate high-quality scientific insights to support clinical development in non-oncology portfolio. This role contributes to the end-to-end delivery of insight-generating projects with minimal supervision and applies scientific and technical expertise to the design, analysis, interpretation, and communication of observational research in real-world settings. This role works in a highly matrixed environment and collaborates with cross-functional colleagues, external partners, and vendors to deliver timely, decision-relevant evidence. **Key Responsibilities:** * **Project execution and co-leadership:** Execute and co-lead RWE projects from research questions through study delivery, ensuring high-quality output and timely completion with minimal supervision. * **Study design expertise:** Serve as a subject matter expert in the design of complex observational studies, including prospective cohort studies, retrospective chart review studies, and insight-generation projects using real-world data etc. * **Scientific input into protocols and analyses:** Contribute to study concepts, protocols, statistical analysis plans, analysis specifications, and interpretation of results to ensure scientific validity and fitness for purpose. * **Data interpretation and insight generation:** Interpret RWE and translate findings into clear, relevant insights regarding patient characteristics, disease burden, treatment patterns, outcomes, and unmet need. * **Cross-functional collaboration:** Partner effectively with internal stakeholders across different functions including TA, development operation, portfolio management, biometrics, regulatory affairs, and medical affairs or commercial teams to align on objectives and deliver evidence that informs decision-making. * **Vendor and partner management:** Indepen
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