A leading biotechnology firm in Cambridge is seeking a Manager of Statistical Programming to lead programming for clinical trials. Responsibilities include overseeing data processing, managing timelines, and ensuring adherence to standards. The ideal candidate has a Master's Degree and 8-10 years of relevant experience in statistical programming, preferably within the biotech or pharmaceutical industries. Strong communication and project management skills are essential for success in this role. Competitive salary and comprehensive benefits offered.
Qualifications
Master's Degree is required.
10+ years of programming in clinical trial data is preferable.
SAS Certification is desirable.
5+ years in project and people management is acceptable.
Responsibilities
Provide timely programming support and project leadership.
Lead programming for clinical study data processing.
Ensure adherence to project standards and guidelines.
Oversee documentation within a regulated environment.
Manage programming deliverables and deadlines.
Skills
Expertise in therapeutic areas
Programming leadership
Statistical programming
Data management
Communication skills
Education
Master's Degree
Tools
SAS
CDISC SDTM / ADaM
Job description
A leading biotechnology firm in Cambridge is seeking a Manager of Statistical Programming to lead programming for clinical trials. Responsibilities include overseeing data processing, managing timelines, and ensuring adherence to standards. The ideal candidate has a Master's Degree and 8-10 years of relevant experience in statistical programming, preferably within the biotech or pharmaceutical industries. Strong communication and project management skills are essential for success in this role. Competitive salary and comprehensive benefits offered.