Support development and validation of datasets, tables, figures, and listings for clinical trials using SAS and/or R.
Assist with CDISC-compliant SDTM and ADaM datasets, Define-XML, and electronic submission deliverables.
Perform programming validation, quality checks, and collaborate with cross-functional teams to meet project timelines.
ClinChoice is a global full-service CRO supporting clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, the company emphasizes a quality-driven one-team culture and continuous employee training.
Lead the statistical design and analytical planning for oncology clinical utility studies with innovative methodologies.
Author and review high-quality statistical deliverables including SAPs and reports for cross-functional collaborators.
Mentor early career statisticians and support continuous improvement of departmental processes and tools.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The team consists of highly dedicated professionals from world-class institutions, working in a fast-paced environment.
Lead biostatistics activities across clinical studies, ensuring high-quality analyses and clear communication.
Provide statistical expertise for oncology trials, from protocol development to regulatory submissions.
Oversee statistical programming and deliverables, ensuring quality, integrity, and compliance.
Jobgether is a platform that uses AI-powered matching to connect candidates with hiring companies, focusing on objective and fair application reviews. The company is dynamic and emphasizes a streamlined hiring process, with a data-driven approach and a commitment to innovation.
Lead technical sales engagements with healthcare and life sciences clients, gathering requirements and demonstrating SLC capabilities.
Conduct proof-of-concept activities and provide architectural guidance for deploying SLC in existing IT ecosystems.
Act as a subject matter expert in SAS language and statistical programming, authoring industry-specific presentations and workshops.
Siemens Software is a leading industrial software company that builds technology to shape the real world. With 30,000 employees across more than 200 countries, we foster a culture of trust, autonomy, and inclusion.
Lead study concept and protocol design, author clinical pharmacology development plans, and conduct PK-PD analyses to support clinical trials.
Provide technical expertise using software such as Phoenix WinNonlin, NLME, R, and NONMEM, and collaborate closely with clients.
Mentor junior pharmacologists, stay current with advancements, and ensure compliance with regulatory requirements.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals across more than 20 countries, they maintain a quality-focused, collaborative 'one-team' culture that emphasizes work-life balance and professional development.
Independently lead statistical design and analysis for preclinical studies, including dose-response modeling and aging biomarker studies.
Build and apply population PK/PD models to support internal dose-justification and formulation decisions.
Conduct exploratory analyses to support endpoint development and target/pathway discovery.
Loyal is a clinical-stage veterinary medicine company developing longevity drugs for dogs. Loyal is a well-funded startup with teams of scientists, veterinarians, engineers, operators, and creatives.
Set the statistical vision and direction for clinical studies spanning early feasibility through post-market evidence generation.
Manage a portfolio of 10+ projects, represent Biostatistics with regulatory agencies, and lead external scientific engagements.
Drive process improvement, mentorship, and AI-enabled productivity across the biostatistics team.
We are a global leader in robotic-assisted surgery and minimally invasive care, with technologies like the da Vinci surgical system. We are a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human.
Provide statistical expertise across clinical development programs, authoring SAPs and overseeing ADaM/TFL deliverables.
Contribute to innovative trial designs, regulatory submissions, and cross-functional collaboration with clinical teams.
Ensure high-quality statistical analyses and compliance with regulatory requirements in a remote/hybrid setting.
The partner company specializes in global clinical development, supporting registration-directed clinical trials across therapeutic areas. It fosters a collaborative, results-oriented culture with a focus on innovation, professional growth, and high-quality deliverables.
Lead the identification, development, and application of innovative statistical methodologies for clinical development programs.
Provide expert statistical consultation and shape statistical strategies for clinical trial design and analysis.
Mentor statisticians and build a statistical innovation team to foster methodological excellence.
Alnylam is the leader in RNAi therapeutics, a revolutionary approach with the potential to transform the lives of people with rare and common diseases. The company is a globally recognized top employer with an authentic, inclusive culture and a deep pipeline, late-stage programs, and a bold vision.
Perform lead biostatistician role providing technical expertise for complex clinical studies.
Develop statistical sections of protocols, analysis plans, and review tables/figures for regulatory submissions.
Partner with statistical programmers to manage timelines and ensure quality deliverables.
Freenome is developing in vitro diagnostic products for early cancer detection through blood tests. The company values diversity and fosters a collaborative, fast-paced culture.
Oversee global clinical trial execution, including site selection, activation, enrollment, and closeout, while ensuring compliance with GCP and regulatory requirements.
Partner with CROs to drive robust trial management, data monitoring, and patient enrollment strategies, and review study-related plans and documents.
Mentor and guide clinical operations team members, track performance metrics, and ensure inspection readiness across all study phases.
Summit Therapeutics is a biopharmaceutical oncology company focused on improving quality of life and resolving unmet medical needs through innovative clinical studies. With multiple global Phase 3 trials and offices across the US, UK, and Ireland, the company is committed to a collaborative, people-driven culture.
Monitor clinical trial sites to ensure compliance with protocols, SOPs, and regulatory requirements.
Review electronic medical records and source documentation for accuracy and data integrity.
Support site staff and contribute to development of trial materials, SOPs, and training guides.
Orca Bio is a commercial-stage biotechnology company developing next-generation cell therapies to improve transplant outcomes for blood cancer patients. The company maintains a start-up culture with an entrepreneurial spirit and emphasis on camaraderie.
Serve as the primary Clinical QA point of contact for a Phase 3, global study.
Collaborate with cross-functional groups to support study start-up and execution.
Perform clinical site audits and support inspection readiness.
Priovant is a biopharmaceutical company committed to developing therapies for autoimmune diseases. They have a small, collaborative team with a hands-on culture.