Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our companys renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools
Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our Companys renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools
Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our Companys renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools
The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses,
Senior Scientist, Statistical Programming Location North Wales, Pennsylvania, United States of America. Full‑time position. This position supports statistical programming activities for late‑stage drug and vaccine clinical development projects, including leadership of one or more projects. The incumbent develops
CSL seeks a Director of Statistical Programming to lead the development and maintenance of CSL’s statistical programming capabilities to meet regulatory obligations. You will manage a team of programmers supporting clinical trials and integrated analyses across therapeutic areas.
The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses,
Job Description Job Title: Database Programmer Location: Horsham, PA Duration: 12+ Months Pay Rate: Best in the market Job Overview The Safety Data Programmer is responsible for providing programming support to internal customers, performing complex Oracle SQL
Program Manager Location: Trenton, NJ 08601 Duration: 6 Months with HIGH possibility of extension This position is for a Program manager to oversee vendors and projects related to the NJ HIN. This resource should have prior
Position Summary The Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with the Director,
Responsibilities Support statistical programming activities for clinical trial data analysis. Develop SAS programs to create and validate analysis datasets (ADaM) and summaries (TFLs) in support of Clinical Study Reports and regulatory submissions (FDA, EMA, etc.). Collaborate with
Sr. Manager/ Associate Director, Statistical Programming Chesterbrook, PA At Avalo (ahh-vah-low), we are 100% focused on developing treatments for immune-mediated inflammatory diseases with large unmet needs that affect millions worldwide. Our strategy is to develop medicines that
Merck & Co. in Montgomery County is seeking a seasoned clinical trial programming expert to lead the development of analysis standards for drug and vaccine projects. This role requires strong strategic thinking and project management skills, with
Madrigalpharma in Conshohocken is hiring a Principal / Associate Director, Statistical Programming, responsible for leading programming activities across clinical development phases. The role demands strong SAS skills and collaboration with various teams to ensure quality and compliance. Candidates
Avalo Therapeutics, located in Chesterbrook, PA, is looking for a Senior Manager/Associate Director, Statistical Programming to lead programming activities for clinical trials and regulatory submissions. The ideal candidate will have a Masters degree in a quantitative field and
Responsibilities Support statistical programming activities for clinical trial data analysis. Develop SAS programs to create and validate analysis datasets (ADaM) and summaries (TFLs) in support of Clinical Study Reports and regulatory submissions (FDA, EMA, etc.). Collaborate with
Our client is seeking an experienced CNC Programmer | Machinist to support production by creating CAM programs, performing full CNC mill setups, designing fixturing, and verifying first‑article parts. This role requires expert‑level CAM programming ability and strong
Dot Net Developer Responsible for building and maintaining internal and external facing web applications for Labors Wage and Hour Compliance division. Likely to extend based on obtain additional funding. This person will be responsible for building
Job Description In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our companys renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state‑of‑the‑art scientific methodologies and tools to
CONTROLS ENGINEER - PLC PROGRAMMING A local OEM is seeking a Controls Engineer with a BSEE (or related degree) and PLC/ HMI programming experience. Your primary duties will include: Programming PLCs and HMIs AutoCAD experience is preferred. Electrical testing