Associate Director, Statistical Programming

Job SummaryAs a Statistical Programmer Lead at BTA, you will provide project leadership and programming support for processing data from clinical studies. Your key responsibilities will include assisting in providing mentorship in implementing and driving programming and project standards, designing and testing program logic, coding programs, and preparing...

Job SummaryWe are seeking a highly skilled Senior Statistical Programmer to lead and support all programming activities for our clinical studies and regulatory submissions. The ideal candidate will have excellent SAS programming skills, a strong understanding of statistical concepts, and the ability to work independently.Key Responsibilities:Lead programming...

The Statistical Programmer provides support to the lead programmer and the study team on all programming activities according to the study requirements and the timelines. The incumbent implements and performs the programming and project standard under general supervision of the lead programmer and manager to support ongoing clinical studies and requests for...

The Senior Statistical Programmer will provide timely support to the study team on all programming matters according to the project strategies. The role will involve project leadership and programming support for processing data from clinical studies. The Senior Statistical Programmer will provide guidance in implementing and performing the programming and...

The Senior Statistical Programmer will provide timely support to the study team on all programming matters according to the project strategies. This role will lead the programming aspect of a project, both internally or with CROs, for all programming results from the single study through to regulatory approval, product launch, data monitoring boards and...

The Senior Statistical Programmer will provide support to the lead programmer and study team on all programming activities according to the study requirements and timelines. The incumbent will implement and execute the programming and project standard under minimal supervision of the lead programmer and manager to support ongoing clinical studies and...

The Senior Statistical Programmer will provide timely support to the study team on all programming matters according to the project strategies. This role will provide project leadership and programming support for processing data from clinical studies. The successful candidate will provide guidance in implementing and performing the programming and project...

Job SummaryThe Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis.Key ResponsibilitiesLead...

The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal...

The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal...

Accelerated Clinical Research Associate ProgramParexel is seeking a Clinical Research Associate to join our Accelerated Program, designed for recent graduates and individuals with less than a year of clinical experience. This program provides foundational clinical research training, including project and system experience, to help you transform into a...

The Clinical Data Management Lead - Associate Director is responsible for the strategic management of Clinical Data Management programs. This individual oversees data management activities, ensuring quality, timelines, and resources are aligned with applicable regulations and company SOPs.This role requires a strong understanding of clinical research and...

Job SummaryThe Clinical Data Management Lead - Associate Director is responsible for the strategic management of clinical data management programs. This individual will lead data management activities and decisions, including quality, timelines, and resources, to ensure the successful conduct of clinical research studies in accordance with applicable...

Description   Associate Director, Employee Relations (ER) Stockley Park Gilead Sciences, Inc. is a global research-based biopharmaceutical company founded in 1987 and headquartered in Foster City, California. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you...

About the RoleThe Associate Director of R&D Corrective Actions Operations Management is responsible for overseeing the R&D CAPA program and associated processes, ensuring its effectiveness and continuous improvement. This role involves managing CAPA administration, CAPA training, setting record standards, and maintaining high-quality standards for records...

The Associate Director for Medical Strategy at Regeneron Pharmaceuticals, Inc. plays a crucial role in the development of medical strategy and planning of medical affairs activities. This position requires a deep understanding of Infectious Disease or a background in Internal Medicine, serving as a scientific and medical resource within the company. The...

The Clinical Data Management Lead - Program Director is responsible for the strategic management of clinical data management programs. This individual oversees data management activities, ensuring quality, timelines, and resources are aligned with applicable regulations and company SOPs.Key Responsibilities:Lead clinical data management programs to ensure...

About RegeneronRegeneron is a talent-hiring platform in Life Sciences, Pharma and IT. We connect talented individuals with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

Job SummaryRegeneron is seeking an experienced Associate Director to lead our Global Patient Safety organization in the Case Evaluation & Reporting area. As a key member of our team, you will be responsible for coordinating pharmacovigilance operations, ensuring efficient vendor and case processing to meet regulatory standards.Key ResponsibilitiesLead all...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...