Job Description:

Senior Clinical Database Programmer

The Senior Clinical Database Programmer will work under the supervision of Principal CDP (or higher-level role) but may work independently as project lead. Working closely with members of Data Management, Statistics, Information Technology (IT), and Quality Control (QC) Departments, the Senior Clinical Database Programmer is responsible for the design and development of electronic and paper Case Report Forms, and to manage, direct, and enable set up of studies using Company’s clinical data management systems, including the maintenance and development of computer programs and processes that support team’s activities, within scope, budget and timelines in compliance with the United Kingdom Statutory Instrument 2004 No. 1031 and its subsequent amendments, ICH guidelines for Good Clinical Practice and other national and international standards and legislation (as required), Company procedures, and client instructions.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

• 105+ approved therapies for marketing applications prepared by Veristat
• 480+ oncology projects in the past 5 years
• 350+ rare disease projects delivered in the past 5 years
• Flexible, inclusive culture — 70% remote workforce, 66% women-led teams

Learn more about our core values here !

What we offer

• The estimated hiring range for this role is $104K to $115K USD plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to skills and experience, licensure and certifications, education, specific location and dynamic market data.
• Benefits vary by location and may include:
  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for

• Bachelor’s degree or equivalent (preferred in science) or equivalent work experience.

• 5-7 years industry and sector experience in eCRF design and development with commercially available CDMS- i.e., Medidata Rave, Oracle InForm/ Central Designer, Veeva, DataLabs, Medrio.

• 4 years’ experience leading eCRF Design/Development/ Maintenance projects and activities without support of a senior colleague.

• Able to lead complex studies.

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.