Lead Statistical Programmer
il y a 9 heures
Hobson Prior are currently looking for a Lead Statistical Programmer to join a brilliant pharmaceutical organisation on a permanent basis with the ability to work remotely from anywhere in the UK, France or Belgium. Our client is focused on discovering and developing innovative treatments for people who suffer from cancer.
Please note that to be considered for this role you must have the right to work in this location.
**Key Responsibilities**:
- For this role, you will be guiding the evolvement of standard SAS Macros and the evolvement of standard operating procedures (SOPs).
- You will preserve coordinated, accomplished and updates project papers, testing and authentication/quality control of reports and programs, guaranteeing promptness for inspection.
- To develop the effectiveness of programming duties and/or develop general quality of programming deliverables, you will recognise gaps, suggest resolutions and implement knowledge.
- Progress and supervise the development of SAS programs for the generation of TLFs.
- Warrant deliverables in a timely manner, that all quality procedures are adhered to and coherent within the projects.
- Monitor the evolvement of SAS programs for the production of ADaM data sets adhering to CDISC standards.
**Key Skills**:
- A self-starter with a dynamic outlook and is resourceful.
- Take on difficulties with practicality and innovativeness.
- Capable of involving the team to accomplish objectives without direct authority.
- An organised individual with the ability to communicate well both verbally and written.
**Requirements**:
- Educated to a degree level in a statistic, computer science, data science/engineering, mathematics or a similar scientific discipline.
- At least 10+ years of experience with clinical programming/clinical data management with increasing accountability, ideally within a pharmaceutical/clinical trial setting.
- Know-how if data structures and pertinent programming languages for data manipulation and documenting which may involve SAS, R, Python, etc., though SAS is necessary.
- Comprehension of the drug development procedures which involves experience within regulatory archiving.
- Industry standards knowledge such as SDTM, ADAM, etc.
- Capable of precisely estimating effort needed for project linked programming actions.
- Familiarity with supplier management supervision.
- Able to efficiently serve as a delegate for statistical programming in cross-functional groups.
- Capable of working well in a team setting under mínimal supervision working on various projects concurrently.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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