Lead statistical activities for clinical trials, primarily in Oncology, and act as the lead statistician overseeing strategy and deliverables.
Author key documents including Statistical Analysis Plans (SAPs), Analysis Database Specifications, and statistical sections of clinical study reports.
Collaborate with cross-functional teams, communicate results to stakeholders, and ensure regulatory compliance with FDA, ICH, and GCP standards.
ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 28 years of experience and 4,000+ professionals across 20+ countries, we foster a quality-driven, one-team culture with below-average turnover and a focus on continuous training.
Lead protocol development including study design and statistical analysis plans for clinical trials.
Provide statistical oversight, mentoring, and training to ensure high-quality project delivery.
Manage statistical activities across projects, ensuring accuracy and consistency with regulatory standards.
ClinChoice is a global full-service CRO specializing in clinical development for pharma, biotech, and medical device companies. With over 4,000 professionals across 20+ countries, they foster a quality-driven, one-team culture and emphasize diversity and low turnover.
Provide high-level consulting services for statistical analysis, reporting, and programming in clinical trials.
Develop and validate statistical analysis plans, randomization schedules, and clinical trial reports.
Mentor statistical programmers and ensure compliance with regulatory guidelines like ICH, GCP, and 21 CFR Part 11.
eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. It is a fast-growing company that has won the 2025 Top Workplaces USA Award for Remote Work and emphasizes an inclusive culture and work-life balance.
Manage all programming aspects of clinical databases from study start to post-lock, ensuring compliance with regulatory guidelines.
Lead operational study teams and provide technical training to end users and junior staff.
Communicate project status to internal teams and clients, and perform project forecasting and budget management.
Precision for Medicine is a life sciences company that provides clinical research services, including database programming and data management. The company is growing and seeks a Principal Database Programmer to join its European team, fostering a collaborative and dynamic work environment.
Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
Create datasets, tables, listings, and figures according to study requirements and CDISC standards.
Collaborate with Biostatistics, Data Management, and Clinical teams to ensure quality and timelines.
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 28 years of experience and 4,000+ professionals across more than 20 countries, we foster a supportive culture with below-industry-average turnover.
Provide expert technical support and leadership in clinical trial reporting using advanced SAS features.
Perform quality control checks and ensure accuracy and consistency of SAS code and output.
Collaborate with cross-functional teams to support electronic submissions and compliance with regulatory standards.
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases. With over 30 years of history, the company is consistently recognized as one of the industry's top places to work, including 14 consecutive years on Science magazine's Top Employers list and one of Fortune’s 100 Best Companies to Work For.
Provide strategic statistical expertise across the full lifecycle of clinical studies, from protocol development to clinical study reporting.
Mentor statisticians and ensure excellence in project delivery while collaborating with multidisciplinary global teams.
Influence complex clinical programs and contribute to the development of new therapies through high-quality data-driven decision-making.
This company provides clinical research services and statistical expertise for early-phase drug development. It fosters an inclusive, collaborative culture with opportunities for career growth and mentorship.
Provide leadership and mentorship across regional clinical trials while ensuring high-quality study execution with minimal travel.
Oversee monitoring visit reports, manage study risks, and ensure compliance with corrective measures at country and regional levels.
Collaborate with cross-functional teams, lead project calls, and deliver training to support data integrity and site performance.
PSI CRO is a privately owned, global Contract Research Organization dedicated to advancing medical science and bringing new therapies to patients worldwide. Founded in 1995, the company has over 3,000 employees and prides itself on long-term stability, having never undergone a merger, acquisition, or company-wide layoffs.
Leads a global team of Statistical Programmers, overseeing SDTM, ADaM, and TLF deliverables.
Ensures quality, budget, and timeline adherence while mentoring team members.
Contributes to process improvements and strategic initiatives to enhance operational efficiency.
Ergomed is a specialist clinical research organization focused on rare disease and oncology clinical trials. They have built a collaborative, international team across multiple continents, valuing teamwork, flexibility, and work-life balance.
Provide senior statistical leadership across clinical development projects in ophthalmology.
Lead statistical analysis plans, study design, and regulatory submissions.
Mentor biostatistics professionals and collaborate with cross-functional teams.
The partner company specializes in clinical research and statistical leadership for ophthalmology programs. It offers a fully remote European work environment with a collaborative culture and opportunities for career development.
Lead the full scope of Biostatistics activities for assigned clinical programs, including study design, analysis, and regulatory submissions.
Collaborate cross-functionally with Clinical, Medical, and Regulatory teams to ensure quality and timely delivery of statistical outputs.
Oversee CROs and internal teams, supervise statistical programming, and drive continuous improvement in biostatistics processes.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. The company is headquartered in Radnor, Pennsylvania and operates as a fully remote organization.
Monitor and oversee progress of clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations.
Coordinate study setup and monitoring activities, including investigator identification, regulatory submissions, and site initiation visits.
Identify potential study risks and propose solutions, while maintaining an impeccable eye for detail and quality outcomes.
Precision for Medicine, Oncology and Rare Disease is a precision medicine CRO that combines novel clinical trial designs, operational and medical experts, and advanced biomarker and data analytics. They pride themselves on high CRA retention rates and a culture where employees feel appreciated and have impact.
Provide statistical oversight and lead complex programs such as NDA/BLA/MAA submissions.
Consult with clients on clinical trial study design and regulatory strategy.
Author statistical analysis plans and review statistical output for accuracy.
Precision Medicine Group provides statistical leadership and support for clinical development, consulting with clients on trial design and regulatory strategy. The company is a global organization that values collaboration, service, and accountability, fostering a culture of mentoring and innovation.
Manage a team of statistical programmers supporting clinical research and ensuring quality, integrity, and timely delivery of programming deliverables.
Provide statistical programming support, oversee development of code for Tables, Listings, and Figures, and ensure compliance with quality processes.
Lead resource planning, manage CROs, and contribute to process improvements and innovation in statistical programming standards.
Penumbra is a global healthcare company focused on innovative therapies, designing and marketing novel products for challenging medical conditions. It sells primarily through a direct sales organization in the US, Europe, Canada, and Australia.
Provide statistical support for clinical trials, including protocol design, analysis plans, and database monitoring.
Serve as biostatistics lead for studies, publications, and regulatory submissions.
Ensure study designs are scientifically sound and meet regulatory requirements for efficacy and safety.
Replimune is a biotechnology company pioneering oncolytic immunotherapies to transform cancer treatment. Founded in 2015, the company values collaboration, boldness, dedication, and honesty.
Develops and analyzes research data using statistical methods, assisting researchers with study protocols and computer analyses.
Manages computer systems, writes programs, and trains others in their use, providing statistical expertise in study design and data analysis.
Consults with investigators to determine research questions, performs appropriate statistical analyses, and documents methods and results in reports.
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. It is a large institution with a diverse academic community, committed to equal opportunity and affirmative action.
Lead and develop clinical operations teams, overseeing oncology trial execution from feasibility to closeout.
Drive process improvements and operational excellence to enhance study delivery and site performance.
Ensure compliance with regulations, manage budgets and resources, and foster stakeholder relationships.
The company is a global clinical development organization focused on advancing oncology therapies through clinical trials. It fosters a collaborative and inclusive work environment with opportunities for professional growth and continuous learning.
Leads the planning, conduct, and oversight of clinical studies per scope of work, ensuring compliance with protocols, SOPs, and regulatory requirements.
Acts as primary clinical point of contact for clients, develops study documents, and drives site feasibility and recruitment strategies.
Manages clinical teams, training, vendor oversight, and ensures data quality and timely deliverables across study phases.
Precision Medicine Group is a clinical research organization that provides outsourced clinical trial management services to pharmaceutical and biotechnology companies. The company fosters a collaborative culture focused on quality and compliance, and employs a team of experienced clinical professionals.
Plan, develop, and oversee scientific content for oncology accounts across multiple therapeutic areas.
Lead client interactions, brand strategy, and the scientific portion of brand planning and business development.
Manage resource allocation, develop SOWs, and identify areas for new and organic growth.
Lockwood collaborates with pharmaceutical, biotech, and medical device clients to develop science-based medical communication strategies. Over a third of its staff hold advanced scientific or medical degrees, and most work remotely, fostering a flexible, work-life balanced culture.