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Sr. SAS Programmer-WA PERM
seeking a Senior level SAS programmer to support programming and testing for multiple Phase I-III oncology studies. This role interacts at varying degrees with Biostatistics, Clinical Data Management, Medical Writing, Clinical Operations, Drug Safety, Regulatory and Medical Management to design, write, and test programs in accordance with company, industry, and regulatory requirements. Responsibilities: o Provide programming support for a variety of clinical development activities including but not limited to creating outputs for: data review, interim analyses, regula...
Tags for this job: Sr. sas programmer, statistical programmer, cdisc, sas programmer, perm sas programmer, clinical programmer
View Sr. SAS Programmer-WA PERM Job - Seattle, WA 98101
Sr. SAS Programmer-NJ work from home
one year contract need for clinical statistical programmer with Questionnaire type data Must have large US or CRO pharma experience. 5 years of programming experience within the pharma industry. 1 year extendable contract • Statistical background • Has experience on questionnaire type of data • Has CDISC ADaM experience
Tags for this job: sr sas programmer, statistical programmer, sas, cdisc, sdtm, adam.
View Sr. SAS Programmer-NJ work from home Job - New Jersey work from home, NJ 08807
Regulatory Submissions Specialist
Long-term Contract or temp-to-perm position for an Experienced In-house Regulatory Submissions Specialist opportunity with a growing Pharma company! The Role and your Responsibilities • Track, monitor and compile IND/CTA/NDA/MAA and annual report submissions • Perform Submission-Ready formatting and QC • Record Retention and study closeout responsibilities Offering long term stability and a small team work environment where you will have a hand in decisions, strategy and be a valued team member. Skills required: • Experience using Microsoft project, ...
Tags for this job: NDA, MAA, eCTD, ISI toolbox, FDA submission, NDA publishing
View Regulatory Submissions Specialist Job - Branford, CT 06405
Clinical Project Manager/Sr. CRA
CLINICAL PROJECT MANAGER/Sr. CRA JOB SUMMARY The clinical project manager or Sr. CRA is expected to: • Coordinate and manage the activities of clinical studies and assigned staff in a manner that ensures all timeframes and targets are met and that costs are kept under control. • Ensure that studies are conducted in compliance with FDA, local regulations and ICH GCP guidelines. • Effectively manage assigned staff to ensure high performance, continuous development and low turnover. The PM is expected to have at a minimum attained a Bachelor degree with a Master’s...
Tags for this job: Clinical Project Manager, Sr. CRA, Research, Pharmaceutical, Biotech, CRA, Dermatology, Science
View Clinical Project Manager/Sr. CRA Job - Mountain Lakes, NJ 07046
Biostatistical Programmer
Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: analysis datasets, statistical tables, figures, listings, Integrated Summaries of Safety (ISS), Integrated Summaries of Efficacy (ISE), electronic submissions and other internal and external requests (e.g., publications). Accessing and converting data to SAS from Database management system ...
Tags for this job: oncology, statistics, programming, SAS, SQL, SAS/BASE, SAS/STAT, PhReg, GLM, Mixed, Lifetest, T-Test, efficacy, TLG
View Biostatistical Programmer Job - Woodcliff Lake, NJ 07677