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.
Collect and interpret information from the Protocol, business development sold strategy & site feasibility team to prepare the site staff for site evaluation visits.
Oversee the execution of Site Activation, site activation strategy, adhering to project timelines.
Lead the process of study start-up to support site evaluation/selection visits on each new study and help get selected sites successfully activated and ready to consent.
Care Access is dedicated to making the future of health better for all by bringing world-class research and health services directly to communities. With hundreds of research locations, mobile clinics, and clinicians across the globe, they focus on ensuring every person has the opportunity to understand their health and access the care they need.
Mentor undergraduate students through the full research process
Guide students in developing feasible, high-quality research questions
Provide structured feedback on research plans, data interpretation, and written research drafts
Inspira Education Group is a fast-growing edtech startup in the US. They democratize access to high-quality coaching so that every student has an equal opportunity to access the best opportunities. They are backed by leading venture capital firms and investors.
Ensures complete study scoping, including testing requirements, facilities and other nuances.
Provides technical details to study team for study designs and updates.
Conducts investigations and assists with implementation of corrective actions, as needed.
ACM Global Laboratories impacts patients and their families by being purposefully patient-driven. Their dedication is reflected in the high-quality work provided by their teams every day around the globe.
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.
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.
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.
Design and execution of ongoing and new clinical studies, contributing to the clinical development plan.
Lead and/or serve as the clinical science representative on clinical studies to deliver high quality data for registration.
Partner with stakeholders to deliver clinical programs for registration and launch.
Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Founded in 2019, they are continuously expanding their presence and global footprint and searching for high-impact individuals.
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.
Perform discovery visits to access sites for research partnerships.
Provide protocol and product/procedural training to clinical sites.
Assist sites with pre-screening patients to ensure appropriateness for clinical study, as applicable.
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our 114,000 colleagues serve people in more than 160 countries, providing a portfolio of life-changing technologies across the spectrum of healthcare.