Statistical Programmer I / II
Role details
Job location
Tech stack
Job description
The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management)., Technical:
- Previous experience with SAS and R.
- Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
- Author, review and approve study TFL shells and dataset specifications
- Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice
- Identify data issues and outliers
- Complete, review and approve CDISC Validation tool reports
- Identify data and standards issues and resolve or escalate as appropriate
- Awareness of emerging standards and associated impact to ongoing and future planned trials
- Maintain proficiency in SAS and awareness of developments
- Maintain study master file documents and any other documents that are required to be audit ready
General:
- Lead internal and client study, project and cross functional team meetings effectively
- Present study updates internally and at client meetings
- Share scientific, technical and practical knowledge within the team and with colleagues
- Perform work in full compliance with applicable internal and client policies, procedures, processes and training
- Build effective collaborative working relationships with internal and client team members
- Ensure learnings are shared across projects or studies
- Develop and provide internal technical training where appropriate
- Lead process improvement initiatives, A local authority organization in Bolton seeks a Principal Asset Management Officer. This role involves leading the Children's Services Department's capital programme, managing projects for school improvements, and ensuring compliance with legislation related to school...
Requirements
- BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)
- At least 4 years of relevant industry experience
Other Information/ Additional Requirements:
- Understanding of clinical drug development process, relevant disease areas, endpoints and study designs
What to expect:
- A warm, friendly working environment in which to thrive both personally and professionally.
- A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level.
- A truly unique CRO that's doing something different when it comes to managing staff, projects and building relationships in the industry.
- The ability to own your role and develop your skills and experience.
Benefits & conditions
We have an exciting opportunity for a Principal or Senior level Statistical Programmer skilled in SAS & R to join us on a permanent basis in the UK. We can offer home and/or office working, training and support and a competitive package., If you're passionate about delivering high-quality deliverables, enjoy mentoring, and want to make a real impact at a company that values your contribution, this role is for you. We offer flexible working options (home or office), comprehensive training, and a competitive package. Apply now!, Department: Academic/Bath Spa University (BSU), University of Suffolk (UoS), Canterbury Christ Church University (CCCU), Oxford Brooks University (OBU) and/or Pearson partnerships Location: Manchester (On-Site) Salary: £51,000 Type of Contract: Full-Time, Permanent (40..., Grade: J scp 35 £46,142 to scp 39 £50,269 Contract: Permanent Essential Qualification: Degree (Level 6) in Architecture, Architectural Technology, Project/Construction Management, or a related discipline.Unfortunately, we are unable to offer sponsorship for this...
