Senior Programmer Analyst

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

📋 Description

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

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

• Execute assigned tasks using Medidata Rave, Oracle Inform, or proprietary software in accordance with SOPs, work instructions, and project specifications.

• Carry out post-production modifications to EDC databases and enhancements to SAS programs, including edit checks, listings, and protocol deviations.

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

• Serve as the subject matter expert and primary point of contact for EDC and SAS technical services concerns.

• Deliver leading statistical programming support for the development and maintenance of SDTM and client standard datasets.

• Create and validate custom/complex SDTM domains and manage external data and reconciliations.

• Develop and implement automation, standardization, and best practices for SDTM programming.

• Plan, execute, and supervise study programming activities, encompassing resource estimation, timelines, quality assurance, and cross-functional/client interactions.

• Conduct peer reviews and quality control of study designs.

• Engage in software validation and process evaluations.

• Monitor advancements in new EDC products.

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

• Identify trends, produce reports and metrics, showcase programming processes, and assist with ECRF and study document design.

⛳️ Requirements

• Preferred university or college degree in life sciences, health sciences, information technology, or related fields.

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

• Equivalent and relevant experience may also be taken into account as a substitute for educational qualifications.

• Proficient in English, both in writing and speaking.

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

• Strong problem-solving abilities and a proactive mindset.

• Effective oral and written communication skills.

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

• Capacity to work effectively within a team setting.

• Ability to work autonomously with minimal supervision.

• Demonstrated interpersonal skills.

🏝️ Benefits

• Medical

• Dental

• Vision

• Life insurance

• Short-term and long-term disability (STD/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