About the Job
The Bioforum Statistical Programming department is expanding, and we are looking for experienced Statistical Programmers to join our growing team in the United Kingdom.
If you are passionate about delivering high-quality output for impactful clinical trials, and enjoy leading programming activities in a collaborative environment, this opportunity is for you.
For this opportunity, oncology trial experience will be a strong advantage.
Required Skills:
- B.Sc degree in Life / Computer Science, Statistics, or equivalent.
- Minimum 5 years’ experience working as a Statistical Programmer. Experience leading a team will be an advantage.
- In-depth knowledge of either CDISC SDTM and/or ADaM standards.
- Advanced knowledge of SAS, including SAS Macros.
- Proven ability to program medium- to high complexity statistical output.
- Excellent communication skills.
- Prior oncology experience and/or team leadership experience is advantageous.
Responsibilities will include:
- For Leads: Lead statistical programming teams to deliver on projects and communicate directly with the sponsor.
- Oversee and/or be responsible for the quality and validation of statistical output produced.
- Create or review SDTM and/or ADaM dataset specifications.
- Program and/or validate SDTM and ADaM datasets, and TLFs.
- Provide guidance and input on the statistical programmer requirements and queries during the conduct of the trial.
Skills Required
- B.Sc in Life/Computer Science, Statistics, or equivalent
- Minimum 5 years experience as a Statistical Programmer
- Experience leading a team
- In-depth knowledge of CDISC SDTM and/or ADaM standards
- Advanced knowledge of SAS, including SAS Macros
- Proven ability to program medium- to high-complexity statistical output
- Excellent communication skills
- Prior oncology trial experience
What We Do
Bioforum is a biometric contract research organization that provides clinical data solutions for pharmaceutical, biotechnology, and medical-device sponsors. Its services include clinical data management, biostatistics, statistical programming, medical writing, data integration, and regulatory-ready reporting. Bioforum helps optimize clinical-trial design, data collection, analysis, and oversight, supporting sponsors throughout the development process and accelerating delivery of new therapies to patients.
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