Principal Programmer: Clinical Database, SAS, R
- Brentford, Greater London (GBR)
- Negotiable
- 12 Months
- Start date: ASAP
- Ref: GSK0JP00087843
- programming
- r
- sas
- datasets
- data management
- therapeutic
- clinical pharmacology
- simulation
- databases
- quantitative
Principal Programmer: Clinical Database, SAS, R
Role is working from Home
Clinical Pharmacology Modelling and Simulation (CPMS) is a science driven group delivering clinical pharmacology and modelling & simulation excellence to development programs. We use quantitative pharmacology approaches, as part of the model-informed drug discovery & development paradigm (MID3), to evolve understanding of compound behavior and optimize dose across the development continuum, delivering a competitive label a filing.
As a member of the CPMS group, you will primarily support the group’s programming requirements while closely collaborating with your counterparts in Clinical Statistics and Data Management. You will be expected find existing data lying on a variety of GSK systems, lead programming efforts and provide expert programming support to colleagues across different therapeutic areas where data aggregation is needed. The programming support will span from early phase studies such as First Time in Human to late phase/registration studies.
Qualifications:
- Bachelors degree in Statistics, Computer, Life/Health Science or related field and at least three years experience in data management and programming in phase I-IV clinical trials.
- Expert programming skills in SAS and R.
- Good understanding of clinical databases.
- Experience of data integration techniques.
- Ability to work effectively in a team environment.
- Proven ability to organize workload and complete tasks on time.
- Ability to multi-task, priorities and adapt to changing timelines.
- Strong interpersonal skills and ability to communicate effectively.
- Understanding of CDISC standards, SDTM and ADaM datasets, Experience with pharmacokinetic data and NONMEM dataset
