Senior Programmer Analyst

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee the development and execution of clinical solutions addressing global technical services challenges related to EDC tools and SAS programming.

• Spearhead the creation of visual analytics dashboards utilizing Spotfire or Tableau.

• Carry out tasks using Medidata Rave, Oracle Inform, or proprietary software in alignment with Fortrea SOPs, work instructions, and project guidelines.

• Execute post-production modifications to EDC databases and enhancements for SAS programs, encompassing edit checks, listings, and protocol deviations.

• Collaborate with Data Managers to review contractual commitments and project timelines.

• Serve as the subject matter expert and primary contact for technical services concerns pertaining to EDC tools or SAS programming.

• Deliver statistical programming assistance for the creation and upkeep of SDTM and client standards datasets.

• Design and validate custom/complex SDTM domains, managing external data and reconciliations.

• Establish and execute SDTM automation, standardization, and optimal programming practices.

• Plan, implement, and supervise study programming tasks, including resource estimation, timelines, quality assurance, and collaboration with various departments and clients.

• Conduct testing, troubleshooting, error resolution, documentation, peer reviews, and quality control of study designs.

• Engage in process evaluations and validation of new or revised software.

• Stay informed about advancements in new EDC products.

• Anticipate resource needs and assign project tasks to team members.

• Recognize trends, produce reports and metrics, showcase programming procedures to sponsors or auditors, and aid in ECRF and study-document design.

• Undertake other assigned responsibilities.

⛳️ Requirements

• A degree from a university or college in life sciences, health sciences, information technology, or a related field is preferred.

• Relevant work experience or education plus experience equivalent to a bachelor's degree may be accepted in lieu of a formal degree.

• Equivalent relevant experience may be taken into account as a substitute for educational prerequisites.

• Proficient in English, both written and spoken.

• 5 to 8 years of pertinent experience in data management and database support, SAS programming, or Spotfire/Tableau development.

• Strong problem-solving abilities and a proactive mindset.

• Excellent oral and written communication skills.

• Basic understanding of clinical trial processes, data management, biometrics, and systems applications is preferred.

• Capacity to work collaboratively within a team setting.

• Ability to work autonomously with minimal supervision.

• Demonstrated interpersonal skills.

🏝️ Benefits

• Medical

• Dental

• Vision

• Life insurance

• Short-term disability (STD)

• Long-term disability (LTD)

• 401(K)

• Paid time off (PTO) or flexible time off (FTO)

• Company bonus, where applicable

• Comprehensive benefits for eligible regular full-time or part-time employees working 20 or more hours per week