Senior SAS Programmer for Regulatory Submissions

Lead Clinical Programming ActivitiesThe Principal Statistical Programmer will oversee and support all programming tasks in line with project strategies, demonstrating the ability to work independently and drive programming efforts for ongoing clinical studies and requests. This includes delivering study reports, regulatory submissions, and ad hoc/post hoc...

We are looking for a talented Clinical Programmer Specialist to join our team at Regeneron. As a Clinical Programmer Specialist, you will be responsible for implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis.About the RoleWork closely with internal...

About This OpportunityRegeneron is seeking a highly skilled Lead Clinical Programmer to join our team in Uxbridge, England. As a key member of our programming team, you will be responsible for leading and supporting all programming activities per project strategies, working independently to implement and drive programming to support ongoing clinical studies...

Job DescriptionWe are seeking an experienced SAS Programmer to lead our clinical data programming team.About the Role:Lead and support all programming activities per project strategies, working independently to implement and drive programming for ongoing clinical studies and requests.Collaborate closely with internal partnering functions, collaborators, and...

About the RoleWe are looking for a highly motivated and experienced Principal Statistical Programmer to join our team. The successful candidate will have proficiency in SAS programming skills, excellent analytical skills, and good knowledge of pharmaceutical clinical development.Key Responsibilities:Lead programming support within multiple...

Regeneron Pharmaceuticals, Inc is offering a highly competitive salary range of $120,000 - $180,000 per year.Job DescriptionWe are seeking an experienced Senior Manager of Regulatory Compliance to provide timely support to the study team on all programming matters according to project strategies. The ideal candidate will lead the programming aspect of a...

Regeneron Pharmaceuticals is a leading biotechnology company dedicated to harnessing the power of biology to create medicines that treat disease and improve human lives.Salary: $106,200.00 - $173,200.00 annuallyThe Principal Statistical Programmer will lead and support all programming activities per project strategies, working independently to implement and...

Job Description">Our Programming Activities and Deliverables Specialist will play a crucial role in leading programming activities for multiple studies/projects in a clinical data environment. This individual will have extensive experience in SAS programming, a strong understanding of pharmaceutical clinical development, and excellent analytical...

Job Title: Lead Clinical Data Programmer We are seeking a skilled and experienced Clinical Data Programmer to join our team at Lifelancer, a talent-hiring platform in Life Sciences, Pharma and IT. As a key member of our programming team, you will be responsible for leading all programming activities per project strategies and implementing programming to...

Regulatory Affairs Senior Associate RoleWe are seeking a highly skilled Regulatory Affairs Senior Associate to join our team at Regeneron Pharmaceuticals Inc.About the RoleThis is an exciting opportunity for a talented individual with a passion for regulatory affairs to support our CMC Regulatory submissions. As a key member of our team, you will play a...

We are looking for a highly skilled Senior Programming Specialist to join our team at Regeneron Pharmaceuticals, Inc.The successful candidate will have good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles). Knowledge of regulatory submissions and requirements is a...

Job Summary">We are seeking a highly skilled Clinical Data Analyst Lead to lead programming activities for multiple studies/projects in a clinical data environment. The ideal candidate will have excellent analytical skills and proficiency in SAS programming with 5+ years of experience preferably in the biotechnology, pharmaceutical, or health-related...

About the RoleAs a Regulatory Affairs Manager, you will play a key role in planning and managing regulatory submissions (e.g., clinical trial and marketing applications) for products within our portfolio in compliance with global filing plans and local regulatory requirements.You will also be responsible for acting as a contact with relevant regulatory...

Regeneron Pharmaceuticals, Inc is seeking a talented Clinical Data Analyst to lead and support all programming activities per the project strategies.The ideal candidate will have proficiency in SAS programming skills in a clinical data environment with excellent analytical skills. Knowledge of other programming languages such as R, Python, etc. is a plus.We...

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...

ResponsibilitiesLead programming support within multiple studies/projects in various study activities to ensure timely and high-quality programming deliverables in assigned projects and areas.Develop and maintain programming documentation and specifications following programming standards and processes.Support global regulatory authority submissions...

About the Role:We are seeking an experienced Regulatory Affairs Senior Manager to join our team in Uxbridge. In this role, you will develop and execute regulatory strategies to ensure compliance with global regulations and our business model. You will collaborate with cross-functional teams to provide regulatory guidance, contribute to product development,...

A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products. This is a great opportunity to work with a team who take provide in...

A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulatory plans across multiple products. This is a great opportunity to work with a team who take provide in...

About the Role:The Regeneron Pharmaceuticals team is seeking a highly skilled Clinical Data Programming Expert to join our team and take on the role of leading programming activities, working independently, and supporting clinical studies and regulatory submissions with high-quality programming deliverables.Main Responsibilities:Leading programming support...