Manager Statistical Programming job in New York, USA

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Job type: Permanent

Discipline: Statistics, Data Management, Programming

Location: United States

This vacancy has now expired. Please see similar roles below...

Proclinical is currently recruiting for a Manager of Statistical Programming with a leading pharmaceutical company located in New York, NY. As the Manager of Statistical Programming, you will perform programming tasks, including coordinating with external vendors as required for clinical, business, and research development.

Job Responsibilities:

Serve as a subject matter expert and provides expertise for programming.
Perform all programming tasks required to support Data Management and Biostatistics, as necessary.
Perform validation and QC/QA of CDISC, SDTM domain output in accordance with SOPs, SOIs, and guidance documents.
Manage external vendors and ensure accurate and high-quality deliverables.
Create and maintain specifications as per CDISC SDTMIG.
Define and create ad-hoc reports and listings for clinical teams.
Develop, implement and maintain SAS programming standards.
Review annotated case report forms and database structures.
Manage or lead programming assignments as necessary.
Mentor and train other associates within Data Management, as necessary.
Participates in the development of and ensure compliance to Standard Operating Procedures (SOPs), policies, and guidelines.
Remain informed of new developments in programming that are relevant to the industry and contribute to the innovation of new reporting systems.
Establish and implement programming standards and comply with regulatory requirements among project team members and across all studies.
Review deliverables before transfer to either internal or external clients.

Skills & Requirements:

BA/BS degree required, MS degree in statistics/mathematics desired.

Minimum of 8 years SAS and clinical programming experience in the biotech/pharmaceutical/ CRO industry.
Project management and team leadership experience.
Knowledge of CDISC, CDASH and SDTM is a must.
Experience with programming development, validation, execution, maintenance, documentation, and archival of clinical data for regulatory submission is required.
Proficient in industry standards, medical terminology, and clinical trial methodologies.
Drug filing experience.
Vendor (CRO) management experience.

If you are having difficulty in applying or if you have any questions, please contact Felix Hook at (+1) 646-367-2617 or f.hook@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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