Everest Clinical Research (Everest) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and
Position Summary Provides statistical leadership and support for all phases of clinical development. Specific responsibilities include consulting with clients regarding clinical trial study design and regulatory strategy, writing and reviewing statistical methods and sample size sections
Key Responsibilities Develop and validate complex analysis datasets (ADaM) and TFLs using SAS. Write and review programming specifications and supporting documentation. Create standard macros and tools to improve efficiency. Serve as a project lead programmer , assigning
Key Responsibilities Develop and validate complex analysis datasets (ADaM) and TFLs using SAS. Write and review programming specifications and supporting documentation. Create standard macros and tools to improve efficiency. Serve as a project lead programmer , assigning
Position Title:Senior/Principal Statistical Programmer Location:Head Office (Toronto, ON) Status:Full-Time Summary: The Principal Statistical Programmer provides high quality programming solutions to support clinical studies in various therapeutic areas. She/he will work closely within a team of SAS
Become a Lead Statistical Programmer at our Toronto headquarters. Bring your SAS expertise to support critical clinical studies while guiding a team to deliver accurate programming solutions. Ideal candidates will hold a BA or BSc in
At Lifebit, were driven by the mission to make complex data analysis simpler and more accessible. We empower key institutions worldwide to revolutionize their data utilization and technology integration. Lifebit is powering the world’s federated data
Who Are You? An experienced Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support or lead one or more Phase I-IV clinical studies. You are excited and
Life Sciences Recruitment Consultant Pairing Biostatisticians with the Top Pharma, Biotech and CROs across the US and Canada Call me on… Principal Biostatistician – RWE (FSP) | Canada | Fully Remote | Permanent We’ve partnered with
About the profile We are seeking a highly motivated and detail-oriented Semantic Data Modeler to join our innovative team. In this role, you will design, develop, and maintain semantic data models that form the backbone of
Join Our Talent CommunityWere not advertising a specific role today - were proactively connecting with experienced professionals for upcoming opportunities. As part of ourteam, you would be working alongside passionate and innovative professionals to ensure our
Job ID R- Date posted 09/16/2026 Responsible to coordinate the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM processes, standards, and technology. Member of the Global Study Team (GST)
JD ID JD0044 Position Name Business Analyst / Life Sciences Consultant About the profile About MIGx MIGx is a global consulting company with an exclusive focus on the healthcare and life science industries, with their particularly
Responsible to coordinate the Clinical Data Management (CDM) deliverables on assigned clinical studies and may be an expert on CDM processes, standards, and technology. Member of the Global Study Team (GST) and the main point of contact
Role Barcelona onsite 3 days office/2 days homeWould you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment? Join
Role Barcelona onsite 3 days office/2 days home Would you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment?