Skip to main content

Clinical Programmer Jobs

1000+ jobs

Immediate Need In the Northern California Bay Area for a: Senior Clinical Data Manager and a Senior SAS Clinical Programmer Solid Pharma Sponsor Start-up in need of two sharp individuals for their growing team. Excellent salaries, benefits and lots of opportunity for growth. 1. Clinical Data Manager: We need someone with heavy "hands-on" clinical CDM experience who can also manage outside CRO...

TalentMine is actively seeking contract Clinical/EDC Programmers for one of our Pharmaceutical clients in the Greater Boston Area. This is a contract opportunity with a excellent company. We are looking for a Clinical/EDC Programmer with a minimum of 5 years of Clinical/EDC Programming experience in Pharmaceutical, Biotechnology, or CRO environment. Candidate MUST HAVE EDC Programming experience. ...

New Contract Opportunity Clinical SAS Programmer Major CRO 6 months Blue Bell, Pennsylvania Clinical SAS Programmer Hi! One of our clients, a major Clinical Research Organization in Blue Bell, Pennsylvania, is looking for a clinical SAS programmer to join them on a contract basis. Responsibilities: Perform project-related analysis programming including writing SAS code to generate analysi...

- Onsite Basking Ridge, NJ - 1 year potentially renewable contract Summary: A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified accordi...

*This position is work from home/remote. Clinical Programmer General Description: Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems. Provide technical expertise in conjunction with internal and external clients. Program, test, and document databases in accordance with programming standards and validation procedures. Program da...

Sr. Clinical SAS Programmer: Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead. Able to support multiple protocols independently and to contribute to integr...

Principal Clinical Data Programmer Responsibilities will include, but are not limited to: • Develop, program, test and maintain clinical trial databases and data entry screens using Oracle Clinical, Medidata Rave and InForm in accordance with company standards. • Develop standard CRF metadata per company standards; contribute to the creation of CDASH compliant CRFs. • Review computer validatio...

SAS Programmer consultant 1 year renewable contract onsite Ridgefield, CT CDISC Experience 1-3 years’ experience supporting clinical trials MS Statistics/BS Computer Science or Math 1. Utilizes SOPs and guidelines, trial protocols, annotated case report forms, Oracle*Clinical study definitions, trial and project data handling rules and standards, and Statistical Analyses Plans in preparation ...

Onsite, Seattle WA, Contract SAS programmer need 6months renewable up to 18 months total duration Responsibilities & Activities: • Develop and validate SAS® programs to produce high quality deliverables within set timelines in accordance with company and regulatory requirements. The deliverables include datasets, tables, listings and figures. • Review and provide feedback on deliverables from ...

Contract Clinical SAS programmer One Year renewable contract A statistical programmer consultant provides timely support to the study team on all programming matters according to the project strategies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent implements and executes the programm...

arge pharmaceutical company in Central NJ has an immediate need for a contract based Oracle Clinical Programmer. Role is onsite and initially 6 months with the option to be extended. Requirements/Duties: BS in computing or a scientific discipline preferred. 3 to 7 years experience in a pharmaceutical company working with clinical trial data is preferred. 1-5+ years experience working with PL/SQL...

Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That’s why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission...

Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That’s why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission...

Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That’s why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission...

Org Marketing Statement All over the world, Pfizer colleagues are working together to positively impact health for everyone, everywhere. Each position at Pfizer touches and contributes to the success of our business and our world. That’s why, as one of the global leaders in the biopharmaceutical industry, Pfizer is committed to seeking out inspired new talent who share our core values and mission...

- Responsible for obtaining goals of statistical group on clinical research studies. - Develops and implements Statistical Programming Specifications and QC plans with lead Statistician for one or more studies. - Works closely with study team to assure quality data and deliverables are met. - Act as liaison to other groups and teams to relay timelines and goals. - At least 5 years of experienc...

- Intermediate knowledge of / experience with SAS software. - Working knowledge of database design/structures. - Good understanding of global clinical trial practices, procedures, methodologies. - Good understanding of regulatory requirements relevant to SR (e.g., GCP, ICH). - Intermediate knowledge of office tools. - At least 4 years' experience in a programming role preferably supporting cl...

Work Location: United States-Tennessee-Nashville-Sarah Cannon Research Institute Clinical Operations Schedule: Full-time Summary of Key Responsibilities: Ensures the development of an accurate clinical study database. Duties and Responsibilities: Duties include but are not limited to: • Ensures the development of an accurate clinical study database according to the study’s protocol and case r...

*This position is work from home/remote.Clinical Programmer General Description: Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems. Provide technical expertise in conjunction with internal and external clients. Program, test, and document databases in accordance with programming standards and validation procedures. Program data...

Advance your career with the company that makes it easier for people to choose better health. Express Scripts is a leading healthcare company serving tens of millions of consumers. We are looking for individuals who are passionate, creative and committed to creating systems and service solutions that promote better health outcomes. Join the company that Fortune magazine ranked as one of the "Most...