[Hiring] Senior Clinical Database Programmer @Veristat

Role Description

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:

• Design and development of electronic and paper Case Report Forms.
• Manage, direct, and enable set up of studies using Company’s clinical data management systems.
• Maintenance and development of computer programs and processes that support team’s activities.
• Ensuring 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.
• Adhering to Company procedures and client instructions.

Qualifications

• 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 (e.g., 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.

Requirements

• Experience in eCRF design and development.
• Leadership skills in managing complex studies.

Benefits

• Remote working.
• Flexible time off.
• Paid holidays.
• Medical insurance.
• Tuition reimbursement.
• Retirement plans.