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Data Management Opportunities at Parexel

Discover Parexel, a premier service provider for the global pharmaceutical industry that can offer you the opportunity to make a profound difference in millions of lives. You'll be immersed in diverse projects that keep you challenged every day, as well as surrounded by colleagues who share your passion and dedication. Bring life-saving treatments to the world with a Data Management job at Parexel. You'll collaborate with a diverse multi-functional team and use an array of technologies on global projects. In addition, our fast-paced environment will give you an opportunity to learn something new every day while you support the accurate collection, organization and analysis of clinical data on small and large studies. Achieve your personal and professional goals with a career in Data Management at Parexel. Our advancement opportunities, individual development and professional growth programs will inspire you to be your best each and every day. If you're a motivated team player, eager to make an impact within Parexel and in the world, join us.

Principal Clinical Database Programmer

Job ID 53895BR United Kingdom - Any Region - Home Based
The Principal Database Programmer will be recognized as a subject matter expert, providing technical support and expert advice to internal and external sponsors. In addition, the Principal Database Programmer can fill the Database Primary (late phase) or Technical Lead role on projects; liaise with sponsors, Data Management Leads and other functional areas as required.
General areas of responsibility also include eCRF design, edit check programming and integration of third party systems with the EDC databases. Further, the Principal Database Programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets. All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements.

Qualifications

Skills:
  • Excellent English written and oral communication skills.
  • Demonstrate ability to learn new systems and function in an evolving technical environment.
  • Attention to detail.
  • Ability to work together with a team (including international teams as required) as well as independently.
  • Work effectively in a quality-focused environment.
  • Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change.
  • Business/Operational skills that include customer focus, commitment to quality management and problem solving.
  • Good business awareness/business development skills (including financial awareness).
  • Work effectively in a quality-focused environment.
  • Strong leadership ability.
  • Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Demonstrate commitment to refine quality processes
  • Demonstrated application of CRS concepts to achieve best practice and promote continuous improvement.
  • Excellent analytical skills.
  • Good presentation skills.
  • Tenacity to work in an innovative environment.
  • Ability to negotiate and influence in order to achieve results.

Knowledge and Experience
  • Proficiency in at least two programming environments (e.g., SAS, CDMS, EDC, SQL, VB, Java).
  • Extensive experience working with RAVE and a preference for additional experience with at least one other system used within the Clinical Trial process (e.g. SAS, CDMS, CTMS, Medical Safety Reporting).
  • Relevant Clinical Trial industry experience.
  • Knowledge of SOPs/Guidelines/Work Instructions/System Life Cycle methodologies, ICHGCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.

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