Average salary: $109,428 /yearly
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- ...electronic regulatory submission. Ensure that all deliverables are completed on time and of high quality. Represent the Clinical Programming function at cross-functional meetings. May support EDC development and visualization tools (PowerBI). Requirements...SuggestedWork experience placement
- ...level documentation • Example outputs and sample displays • Integrated Case Report Forms (iCRFs) • Reviewer documentation: ○ Clinical Study Reviewer’s Guide (cSDRG) ○ ADaM Reviewer’s Guide (aDRG) • Variable derivation documentation and codelist mappings •...Suggested
- ...using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s) Produces and delivers CDISC and regulatory... ...validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs Programs...Suggested
- ...Responsibilities: Develop and maintain SAS programs to import, clean, and validate clinical trial data. Use R for data manipulation, analysis, and visualization. Perform statistical analyses in accordance with study protocols and analysis plans. Generate...Suggested
- ...Responsibilities: The Sr. Statistical Programmer supports the Biostatistics team in the generation and validation of analysis datasets and statistical outputs for clinical trials This role is key to implementing programming standards and supporting the standardization...SuggestedInterim role
- A leading biotechnology company in Parsippany-Troy Hills is seeking a Senior Associate in Clinical Programming, focusing on managing clinical databases and programming deliverables for clinical development programs. The ideal candidate should have a strong background in...Suggested
- ...Job Description: Performs all SAS programming required for clinical trial analysis and reporting. Ensures that activities and processes... ...the guidance of the project statistician. Acts as primary programmer to produce tables, listings, and figures for the clinical...Suggested
- A global leader in clinical research services is seeking a Statistical Programmer in Durham, North Carolina. This role involves developing R packages for clinical trial analysis, validating outputs, and ensuring data integrity. The ideal candidate will have extensive R...Suggested
- Clinical SAS Programmer - Katalyst CRO Join to apply for the Clinical SAS Programmer role at Katalyst CRO Responsibilities Effectively manage and oversee statistical programming resources including contractors and CROs related to statistical programming deliverables to...SuggestedContract workFor contractors
- ...leading biotechnology company is seeking an Analytical Data Science Programmer in Boston to transform statistical analysis plans into high-... .... Ideal candidates will have extensive experience in clinical development and proficiency in programming languages like SAS...Suggested
- Join to apply for the Clinical SAS Programmer role at Katalyst CRO 3 days ago Be among the first 25 applicants Join to apply for the Clinical SAS Programmer role at Katalyst CRO Get AI-powered advice on this job and more exclusive features. Responsibilities Engage...SuggestedContract work
- A global healthcare leader based in Indianapolis is seeking an Advisor, Clinical Study Build Programmer to contribute to clinical trial design and execution. This role involves developing robust study databases and ensuring quality and timelines for clinical projects. Candidates...Suggested
- A leading biotechnology firm is seeking a Principal Statistical Programmer in Cambridge, MA, to provide programming support for clinical studies. This role involves leadership in data processing, validation of submissions, and collaboration with a multidisciplinary team...Suggested
- A pharmaceutical services company is seeking a Statistical Programmer in Austin, Texas to design, code, and ensure compliance of datasets for clinical trials. The ideal candidate will have a Master's or Bachelor's degree in Statistics or related fields, with a strong focus...SuggestedContract work
$126k - $204.6k
...to develop creative solutions to support communities through philanthropy and volunteerism. Job Summary The Advisor, Clinical Study Build Programmer, contributes to the successful design and execution of clinical trials by developing and maintaining robust clinical study...SuggestedFull timeWork at officeFlexible hours$140k - $198k
Our Clinical team is seeking a hands‑on strategic Senior Manager, Clinical Statistical Programmer, reporting to our Director of Biostatistics. The ideal candidate will have a proven track record of successfully leading clinical safety analysis and programming across multiple...Summer workWork at officeFlexible hours$100k - $166.6k
A leading medical technology firm is seeking a Senior SAS Programmer based in Mahwah, New Jersey. This onsite role involves implementing SAS programming for clinical trials, generating reports, and providing statistical analysis support for FDA submissions. The ideal candidate...$98.2k - $273.2k
A leading clinical research organization is seeking a Principal Statistical Programmer to provide comprehensive statistical programming support for clinical studies. This role requires deep technical expertise in SDTM, ADaM, and TLF development, along with regulatory submission...- A reputable workforce solutions company is seeking a SAS Programmer for clinical trial analysis in South San Francisco, California. This role involves performing SAS programming, ensuring compliance with sponsor requirements, and collaborating with Biostatistics and Data...
- A clinical research organization in Cincinnati, Ohio is seeking a proficient Statistical Programmer. You'll be tasked with converting specifications into SAS code to generate datasets for clinical trials, managing project deliverables, and developing standardized macros...
- A clinical research organization is looking for a Statistical Programmer in Jacksonville, Florida. The ideal candidate will have expertise in SAS programming and statistical reporting, with a requirement of a Master's degree and at least 3 years of experience or a Bachelor...
- ...biotech company in Cambridge is seeking a Principal Statistical Programmer to provide expert-level programming support. The role involves... ...of experience in SAS programming and a solid understanding of clinical trial methodologies. This position offers a competitive salary...
$112k - $132.1k
A leading research institution in Boston is seeking a Senior Software Engineer to develop innovative research and clinical applications. Candidates will be responsible for coding new features, writing technical documentation, and leading discussions with stakeholders....- A leading clinical research organization is seeking a skilled professional to support phase 3 clinical trials. The ideal candidate will have a Master's degree in Biostatistics and extensive experience in SAS programming and clinical data standards. This role involves ensuring...
- ...Software Engineer for its Corporate Information Services Department. This role focuses on designing, developing, and maintaining custom clinical applications. Applicants should have relevant education and experience in programming, knowledge of HTML, JavaScript, and CSS is...
- A clinical research organization in Chicago is seeking a Statistical Programmer with expertise in SAS programming to support both early and late-phase clinical trials. The ideal candidate will have a master's or bachelor's in Statistics or Computer Science and proven experience...
$69.3k - $173.2k
...global healthcare solutions provider is seeking a Principal Statistical Programmer in Durham, North Carolina. This role involves developing R packages and conducting statistical programming for clinical trials. The ideal candidate will have strong skills in R programming,...- A leading biopharmaceutical company in California is seeking an experienced statistical programmer to design and develop SAS programs for clinical data evaluation. The role requires strong project management skills, proficiency in SAS, and the ability to generate analysis...
$88.3k - $220.9k
...environment of a prominent Pharma company. This Epidemiological Programmer role sits within our Real World Solutions team and will be... ...multiple tasks and projects IQVIA is a leading global provider of clinical research services, commercial insights and healthcare...Full timePart timeImmediate startWorldwide- ...is highly preferred. The ideal candidate must be able to communicate effectively within a multi-disciplinary project team to assess priorities and complete assigned tasks on time. Proficient of SAS programming in a regulated clinical research environment....
