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.
The role of the Clinical Data Coder I (CDC I) is to perform assigned tasks or activities in clinical data management coding. Activities may include user acceptance testing (UAT), coding, data validation, generation and integration of queries, and running of reports under supervision of senior coder team members and/or line manager. Under direct supervision begins to learn the Principal CDC role.
All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instruction/Guidelines, ICH-GCP and/or other international regulatory requirements.
Demonstrates competence while performing activities including:
May include User Acceptance Testing
Data validation and cleaning associated to verbatim requiring coding
Generation and integration of data queries
Coding data reconciliation tasks
Support site monitoring personnel to retrieve coding data as required
Provide work status updates regularly to direct supervisor
Other assigned responsibilities as needed
Previous relevant coding, data management work experience required; clinical and/ or research experience required.
Good interpersonal, verbal and written communication skills
Awareness of all relevant regulations, including ICH-GCP, 21 CFR 11
Knowledge of medical terminology and awareness of coding dictionaries (e.g.MedDRA & WHODrug)
Ability to work in team environment
Good analytical skills and attention to detail
Effective time management to meet daily metrics or team objectives, completion of assigned tasks in a timely manner