- Merck & Co. (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer ... Engineering or related field plus 7 or more years SAS programming experience in a clinical trial...more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent… more
- Merck & Co. (Rahway, NJ)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial environment OR a ... Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial...5 years SAS programming experience in a clinical trial environment.Minimum requirement:Must have experience in CDISC SDTM… more
- Merck & Co. (North Wales, PA)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment MS in ... Life Sciences, Engineering or related field plus 3-7 years SAS programming experience in a clinical trial...3-7 years SAS programming experience in a clinical trial environment - Department Required Skills and Experience:… more
- Eisai, Inc (Nutley, NJ)
- …responsible for implementing new technological solutions for end users.The Associate Director, Clinical Programming manages and oversees JReview and SAS program ... Director of Clinical Programming is the senior level highly technical SAS and JReview programmers. Responsibilities Include but are not limited to: Manage,… more
- Merck & Co. (Rahway, NJ)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environmentMS in Computer ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environmentDepartment Required Skills and Experience: Effective interpersonal… more
- Merck & Co. (Rahway, NJ)
- …Mathematics, Life Sciences, Engineering or related field plus at least 2 years SAS programming experience in a clinical trial environment.Required Experience and ... the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other programming colleagues and biostatisticians and/or… more
- Merck & Co. (Rahway, NJ)
- …Mathematics, Life Sciences, Engineering or related field plus at least 2 years SAS programming experience in a clinical trial environment. Required experience ... graphics for inclusion in study reports and regulatory submissions.Produce SAS transport files and associated documentation for regulatory submissions.Assure...and skills Must possess SAS programming skills including data steps, procedures, SAS… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …implementation. required- Advanced working knowledge of all aspects of the R and SAS programming language used in clinical trials programming. required- Advanced ... signaling detections and across compounds safety reviews (ie, ILD). Collaborate with Clinical Development and Clinical Sciences for effective data surveillance… more
- Genmab (NJ)
- …Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by developing and ... writing corresponding SAS or other programs. The Senior Programming Manager may...of data consistenciesSupports specification and pooling of data across clinical trials within the same project.Supports in-house production of… more
- Merck & Co. (Rahway, NJ)
- …projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory, Statistical Programming, Data Management and other company Research ... Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical...design.-Working knowledge of -statistical and data processing software eg SAS and/or R.-Good oral and written communication skills. Able… more
- Merck & Co. (Rahway, NJ)
- …strategy, and payer/stakeholder communication tools in collaboration with Commercial, Clinical Development, Outcomes Research, Medical Affairs, Policy and regional ... ensuring access considerations are integrated into asset development plans. including clinical and commercial, taking informed positions related to price, value and… more
- Aequor (Thousand Oaks, CA)
- …design and implementation of both new technologies, new processes.Job Description: Clinical Trial Delivery Operating Model: Develop Data Management playbook to ... efficiencies and reduce hand offs. Collaborate with cross-functional teams ( clinical operations, site management, biostatistics, stats programming, TA) to optimize… more
- Katalyst HealthCares and Life Sciences (Boys Town, NE)
- …data cleaning. Oversees and manages Contract Research Organizations (CROs). Develops and tests SAS codes for clinical trial database logic checks. Assign tasks ... Minimum 8 years of experience in statistical programming in a clinical trial environment. SAS programming at an expert level. Understanding of the drug… more
- Beam Therapeutics (Cambridge, MA)
- …statistical programming functions within a therapeutic area to support various clinical studies and submissions to ensure successful execution for Beam's ... clinical programs. In this role, you will work with...head of statistical programming to develop statistical programming strategies, SAS programming infrastructure as well as department standards, applications… more
- System One Holdings, LLC (Carnegie, PA)
- …EMA) and Good Clinical Practices (GCP). Use statistical software such as SAS , R, or STATA for data analysis. Stay current with new developments in biostatistics ... research setting. Proficiency in statistical programming languages such as SAS , R, or STATA. Strong knowledge of clinical... SAS , R, or STATA. Strong knowledge of clinical trial design, statistical methods, and regulatory requirements (FDA,… more
- eTeam, Inc. (Fort Lauderdale, FL)
- …while working in the SAS , R and Python programming environments during the clinical trial phase of the R&D Process. As an IT Business Analyst for the Statistical ... Business Analyst, preferably within the pharmaceutical or life sciences industry. Clinical research and development Understanding GXP systems Job Requirements: We… more
- University of Southern California (Los Angeles, CA)
- …field. Experience in statistical programming using standard statistical packages (eg, SAS , R, STATA). Working knowledge of regulatory Data Standards (eg, ... CDISC/ADaM). Knowledge of clinical research regulatory requirements (eg, Good Clinical Practice [ICH / GCP], FDA / CFR). Ability to interact productively as part… more
- Trilogy (Chicago, IL)
- …one on one services to clients that focus on substance use goals. Acquire a SAS credential within 12 months of hire Recognize and act on opportunities to move ... in any other field with two years of supervised clinical experience in a mental health setting High School...School Diploma or GED and five years of supervised clinical experience in a mental health setting. Minimum one… more
- destinationone Consulting (Los Angeles, CA)
- …research. Key Responsibilities: Design and analyze epidemiological studies and clinical trials. Develop statistical models to interpret health data. Collaborate ... or related field; Ph.D. preferred. Proficiency in statistical software (eg, R, SAS , STATA). Strong analytical and problem-solving skills. Experience in public health… more
- Commonspirit Health (Santa Cruz, CA)
- …with these in healthcare practices and activities. 5. Knowledge of analytical and clinical management tools like PowerBi, Tableau, SAS , Microsoft office, Google ... Health and external data sources and systems including, but not limited to, clinical process and outcome data, electronic health record data, event reporting data,… more
