Function as lead programmer to produce and/or validate tables, listings, figures, and analysis datasets.
Develop/review TFL shells, SDTM and ADaM specifications in collaboration with biostatisticians and other clinical development colleagues.
Work closely with Data Management and Biostatistics to ensure final databases, analyses, and reports are accurate.
Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer using its expertise in chemistry. Nuvalent is an early-stage company bringing together experienced scientists and industry veterans with a proven track record in oncology drug development.
Lead statistical programming efforts for clinical studies.
Oversee and coordinate activities with Contract Research Organizations (CROs).
Collaborate closely with statisticians and cross-functional study teams to deliver results in a timely and accurate manner.
Kailera is developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, they are working together to advance novel therapies for obesity and related conditions.
Provide statistical leadership for oncology clinical trials across multiple phases (Phase I–III).
Lead the development of statistical analysis plans (SAPs), protocols, and clinical study reports (CSRs).
Design and review statistical methodologies for efficacy and safety analyses.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Lead statistical strategy for hematology studies across phases of development.
Oversee generation and validation of TLFs and other statistical outputs.
Contribute to IND, NDA/BLA, and other global submissions.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Lead statistical support for early- and late-phase clinical studies.
Lead the development, execution, and interpretation of statistical analyses.
Lead the development and the adoption of innovative statistical approaches.
Kailera develops therapies that give people the power to transform their lives and elevate their overall health. They are rooted in an entrepreneurial spirit and a team-oriented culture, working together to advance novel therapies for obesity and related conditions.
Lead the development of statistical sections of clinical study protocols and statistical analysis plans.
Provide strategic input to optimize trial designs in early phase dose escalation studies and late phase registrational studies.
Oversee CRO statistical activities and manage contractor statisticians.
Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.
Maintains responsibility of assigned projects and ensures on-time delivery.
Provides input and guidance to the design of clinical databases.
Develops, tests, and validates programs and clinical databases.
Precision Medicine Group is committed to improving the efficiency of medical treatments. They focus on applying precision medicine, supported by data, to enhance research and development in the healthcare sector and is an equal opportunity employer.
Data preparation and cleaning of raw clinical trial data for PK/PD analysis.
Writing R or Rmarkdown code for descriptive and statistical analysis of PK/PD data.
Ensuring CDISC compliance for regulatory submissions.
Jobgether uses an AI-powered matching process to ensure applications are reviewed quickly, objectively, and fairly. They identify top-fitting candidates and share the shortlist with the hiring company.
Ownership of scientific and operational statistical work for clinical trials.
Develop study Statistical Analysis Plans and study documents.
Provide statistical expertise in support of interactions with regulatory agencies.
Tarsus is dedicated to attracting and retaining top talent. The company offers comprehensive benefits, bonus, and stock equity to promote work-life balance.
Provide statistical strategy and oversight for multiple clinical studies.
Design studies, author and review protocols and Statistical Analysis Plans.
Support regulatory submissions, including health authority interactions.
Deciphera is committed to equal employment opportunity and values diversity. The company believes in providing a competitive compensation and benefits package to all employees and has an outstanding culture and opportunities for personal and professional growth.
Provide medical expertise and leadership in clinical development strategies aligned with company objectives.
Lead the development of clinical trial protocols, ensuring scientific rigor and compliance with global regulatory requirements.
Serve as medical monitor for clinical trials and ensure adherence to ICH GCP, patient safety, and data integrity.
Ipsen is a mid-sized global biopharmaceutical company focused on transformative medicines in Oncology, Rare Disease, and Neuroscience. With nearly 100 years of experience and global hubs in the U.S., France, and the U.K, they are committed to a culture of collaboration, excellence, and impact and empower every individual to be their true selves and grow alongside the company’s success.
Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.
Responsible for assuring that data for statistical analyses are complete, accurate and consistent.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific with a strong focus on quality, professional development, and supportive culture.