Jobs at Cytel

Lead strategic statistical consulting engagements, design innovative statistical and clinical development solutions, build client relationships, grow business, mentor consulting teams, represent Cytel externally, and travel regularly to engage senior stakeholders.

The Senior Director, Business Development will drive Cytel’s Pharma client relationships, create strategic sales plans, and oversee client-focused initiatives to expand business growth.

Lead statistical programming for real-world evidence and epidemiology studies: prepare and link RWD (claims/EHR), implement analytic plans, conduct regression and survival analyses, produce tables/figures, liaise with vendors and stakeholders, and support study reports and presentations.

Lead global IT strategy and operations for a life‑sciences CRO: oversee cloud and infrastructure, cybersecurity and compliance (GxP/21 CFR/GDPR), enterprise applications and data strategy, digital transformation, vendor and budget management, and build a global IT organization to enable clinical research, data science, and product delivery.

Provide statistical support for German HTA (AMNOG) dossiers, collaborate with interdisciplinary teams, deliver and QC (re-)analyses per SAP, contribute to templates and methods, present methodology to stakeholders, and ensure compliance with guidelines.

Lead and expand Cytel's large pharma accounts by managing global sales teams, creating and executing strategic account and sales plans, driving RFP/RFI responses and proposals, engaging stakeholders across organizations, and representing Cytel at industry events to win clinical trial and biometrics business.

The role involves developing and closing software business in clinical research organizations, executing sales strategies, and maintaining client relationships in the biopharmaceutical space.

The Sales Operations Lead defines and executes sales strategies, optimizes operations, partners with executives, and leads high-performing teams to drive revenue growth.

Lead post-submission and RWE evidence generation using CDISC, claims, and biological data. Create SAP, contribute to CRF/protocol, produce high-quality statistical programming, consult with clinical scientists, manage stakeholder expectations, and identify analysis limitations.

Lead or support Phase I-III clinical studies (Alzheimer's, Type 2 Diabetes) by designing studies, calculating sample sizes, writing SAPs, performing and interpreting statistical analyses, preparing clinical study reports and submissions, ensuring CDISC/ADaM compliance, QCing outputs with SAS/R, and collaborating with cross-functional teams.

The role involves providing strategic statistical advice, developing innovative solutions for clients in the biopharmaceutical sector, and leading consulting projects to enhance brand recognition and client relationships.

Lead statistical activities for clinical trials from protocol design through reporting. Provide statistical oversight, collaborate with cross-functional teams and CROs, apply SAS/R (and ML) for analyses, automate processes, and mentor junior statisticians.