Senior Programmer Analyst - fully home-based
Joining Fortrea’s Clinical Data Management sponsor dedicated team will offer a rewarding career, a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. With the support of exceptional people from across the globe and a vast array of career options, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.
The Senior Programmer Analyst role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. You will be responsible for the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE.
What you can expect from us
* Office based or home based anywhere in the listed countries
* Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
* Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
* A genuine work life balance
* Flexibility in working hours
* A thorough onboarding with support from your personal mentor
* A permanent employment contract with Fortrea and a rewarding career progression
Your responsibilities
* Lead development and implementation of clinical solutions for EDC tools (e.g., Medidata Rave) and SAS programming issues.
* Serve as SME and primary contact for technical services related to EDC systems and SAS programming.
* Design and develop visual analytics dashboards using tools like Spotfire and Tableau.
* Provide programming support for SDTM/Client standard datasets, including complex domain development, automation, and external data reconciliation.
* Manage and oversee study programming activities: planning, resource estimation, timelines, and client communication.
* Perform and document post-production changes to EDC databases and SAS programs (edit checks, listings, deviations).
* Conduct peer reviews, ensure quality control, and promote best programming practices and process improvements.
* Mentor team members, manage resource allocation, and stay updated on advancements in clinical data tools and system
Your profile
* University / college degree (life sciences, health sciences, information technology or related subjects preferred)
* Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor’s degree
* Fluent in English, both written and verbal
* 5 to 8 years of relevant work experience to include data management and database support or SAS Programming or Spotfire or Tableau development
* Good problem-solving skills and a proactive approach
* Good oral and written communication skills
* Basic knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred
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