Senior Clinical Database Programmer

Veristat•Massachusetts, MA

10d•$104,000 - $115,000•Remote

About The Position

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!

Requirements

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.

Responsibilities

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
Ensure work is completed within scope, budget and timelines
Ensure 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.