Clinical Data Configuration Manager

Veramed is a Clinical Research Organization (CRO) that provides expert data management, biostatistics and programming services to the pharmaceutical and biotech industry. With precision, consistency and an unwavering commitment to quality, Veramed is dedicated to setting the highest standards for biometrics in clinical trials.

Founded in 2012, Veramed has always been guided by quality, integrity and humanity. This means a culture that genuinely cares for its employees, and employees that genuinely care about the work they do, enabling unparalleled collaboration for industry-leading delivery. 

Veramed’s growing team of expert data managers, statisticians and statistical programmers supports analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas. Whether it’s long-term partnerships or rapid-fire project work, Veramed works as an extension of clients’ teams, driving efficient, dependable outcomes. 

A truly global CRO, Veramed is headquartered in Twickenham, England, with offices across the UK, Europe, US and India. Veramed is proud to be B Corp Certified ®, committed to integrity and impact in everything we do. 

Our vision 

We exist to set the new standard for biometrics. By making the right decisions – for our employees, for sponsors, and for patients – we’re redefining what biometrics can deliver in clinical trials.

Purpose of the role

The Clinical Data Configuration Manager sits within R&D’s Testing, Innovation, and Data Enablement organisation and supports clinical study execution by configuring study-level clinical data extractions, transformations, visualisations, and transfers across multiple data sources in alignment with Data Transfer Agreements and technical specifications. This role partners with internal and external stakeholders (including data engineers) to deliver accurate, high quality data in required formats and frequencies , contributes to the development and training of transfer standards/ SOPs and best practices, and provides quality oversight and team capability support (including mentoring/training others and vendor /FSP oversight as needed) to ensure consistent, on time delivery.

Accountabilities:

• Configure study-level clinical data extraction, transformation, and transfer outputs across multiple data sources per Data Transfer Agreement/specifications.
• Partner closely with internal/external stakeholders (including Data Engineers) to deliver required data formats/frequencies with high quality and on time.
• Support implementation of sponsor-defined data transfer standards and specifications.
• Provide input to documentation and training materials as requested.
• Perform/coordinate quality review of configuration and deliverables, including oversight/review of vendor-performed work as needed.
• Support team capability by managing and training other team members; complete other assigned duties within timelines.

Education:

• Bachelor's degree  (e g., CS, Statistics,/Biostatistics, math, biology/heath related) plus minimum 5 years relevant experience (or equivalent experience).
• Experience with EDC build/data management or EDC extraction/configuration; strong understanding of clinical data flow (CDMS, vendor devices, CDR). 
• Familiarity with data cleaning tools (e.g. Veeva CDB, J Review, Elluminate); Strong clinical trial terminology and data transfer specification knowledge; understanding of SDTM.
• Data/Integration: XMLs, APIs, MDR (preferred); ETL/ELT experience
• Programming (preferred): One or more SQL, SAS, R or Python; R Shiny/Python app development.
• Tools/ways of working: Microsoft Office
• Independent and collaborative problem-solving; ability to prioritize and work in a fast-paced environment.
• Strong project management skills including: Initiative, deadline management, strong attention to detail, organization, time management; quick learner comfortable with new tech/systems.