Senior Clinical Solution Analyst responsible for translating study protocols into high-quality study builds and serving as the product subject matter expert to both the Evinova study team and customers.
Compensation
Competitive + Excellent Benefits
Responsibilities
Drive study design, requirements gathering, specification drafting and configuration activities for customer projects
Serve as the product SME within the Delivery organization for product capabilities
Ensure delivery excellence across all phases of global study execution
Work closely with Delivery leadership and Product teams to improve processes
Partner with Commercial team for pre-sales support
Requirements
Bachelor’s degree in Life Sciences, Health Informatics, or related field
Act as the global medical expert and Medical Affairs lead for Karo’s Skin Health portfolio, supporting brands including ACO, Miniderm, Canoderm, Decubal, E45, Biodermal, Iwostin and Emolium.
Locations (2)
Stockholm, Stockholm County, Sweden
Maidenhead, England, United Kingdom
Responsibilities
Provide medical and scientific input into global category, portfolio, brand, innovation and lifecycle strategies.
Translate clinical evidence, scientific insights and healthcare professional perspectives into clear recommendations and business decisions.
Identify evidence gaps and develop medical evidence plans aligned with portfolio priorities, claims, lifecycle opportunities and HCP needs.
Lead or medically oversee clinical research, Phase IV studies, real‑world evidence, registries and observational studies in collaboration with Clinical Operations and cross‑functional teams.
Contribute to study concepts, protocols, endpoints, investigator engagement, interpretation, publication planning and scientific dissemination.
Requirements
Advanced academic degree in life sciences, such as an MSc in Pharmacy, MD, PhD or another relevant scientific qualification.
Lead scientific activities for clinical research programs supporting product development, regulatory approvals, post‑market evidence generation, and scientific communication.
Compensation
The base pay for this position is $78,000.00 – $156,000.00
Responsibilities
Lead development of clinical study protocols, protocol amendments, investigator brochures, case report forms, statistical assumptions, endpoint strategies, and clinical study reports.
Design prospective clinical studies, registries, observational studies, post‑market studies, and evidence‑generation programs supporting global regulatory and business objectives.
Serve as scientific lead for assigned clinical studies and provide strategic scientific direction throughout study planning, execution, analysis, and reporting.
Develop scientific rationale supporting study design, endpoint selection, evidence‑generation strategies, and clinical development plans.
Collaborate with biostatistics to review statistical analysis plans and interpret primary, secondary, subgroup, sensitivity, and safety analyses.
Requirements
Bachelor's degree in Life Sciences, Biological Sciences, Biomedical Sciences, Biomedical Engineering, Bioengineering, Public Health, Epidemiology, Nursing, Medicine, Pharmacy, or related scientific discipline.
Provide clinical and scientific leadership for medical affairs activities, generating and communicating medical evidence to support healthcare decisions.
Compensation
The expected salary range for this position based on the primary location of South San Francisco, CA is $198,600 - 471,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
Responsibilities
Design, execute, and monitor medical strategies, plans and tactics spanning the lifecycle
Provide clinically meaningful perspective for regulatory and other scientific communications
Lead fit‑for‑purpose teams in a matrix environment
Engage with internal and external stakeholders to develop medical strategy
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