Job Description
How you'll make an impact:- As the Director of Statistical Programming, you will lead teams of programmers to develop, test, validate, document, maintain and execute programs in SAS to support statistical deliverables within agreed timelines. He/she will mentor and develop programmers and allocate statistical programming resources under the provided project priorities and timeline.
- Facilitate talent management activities to include hiring, training, staff development and succession planning. Mentor and develop team of programmers by providing regular coaching and guidance. Manage people resource allocation of statistical programming.
- Prepare, document, and review programming codes and output for own project and/or as needed to ensure the quality of programming output.
- Review ADS Specs and output for own project and/or other projects
- Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming, reporting, and review
- Participate in the development of procedures and standards and adherence to existing procedures
- Prepare analysis datasets
- Develop program specification and design documents
What you'll need (Required):- Master's Degree in Computer Science or Statistics or other related fields
- 11 Year experience Solid SAS programming experience on clinical data in the pharmaceutical and/or medical device industry.
- 3 years' experience Managing statistical programmers
What else we look for (Preferred):- Proven successful project management leadership skills
- Proven expertise in SAS and Windows operating systems required; experience using other software packages (e.g., R, S-Plus)
- Proven expertise in MS Office Suite including Word, PowerPoint, Access, and Excel
- Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
- Keeps abreast of new developments in statistics and regulatory guidance
- Expert understanding of clinical trial and statistical programming procedures while addressing issues with impact beyond own team based on knowledge of related disciplines
- Demonstrated track record in people management
- Expert understanding and knowledge relevant to statistical programming
- Expert understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device research setting
- Excellent problem-solving, organizational, analytical and critical thinking skills
- Demonstrated ability to manage assigned team and provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations
- Experience in facilitating change, including collaboration with management and executive stakeholder
- Strict attention to detail
- Ability to interact professionally with all organizational levels
- Ability to manage competing priorities in a fast paced environment
- Must be able to work in a team environment, including participating and presenting at meetings, including with external representatives
- Frequently interacts with customers, and/or functional peer group managers, normally involving matters between cross-functional teams and the company; often leads a cooperative effort among members of a project team
- Participate and present at meetings with internal and external representatives
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The base pay range for this position is $182,000 to $257,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., geographic location, qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
