Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based eClinical Coordinator to join our Data Management team. By working with the eClinical Project Manager and other team members, these professionals ensure the accuracy of data that is reported by patients for clinical studies. If you are detail-oriented, and enjoy a predictable and standardized work environment, this could be the opportunity for you. As new hires, eClinical Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field.
Responsibilities:
- Partner with eClinical Managers and Sponsors to develop and configure device applications unique to each study’s needs
- Support management of device inventory and oversee global shipping and distribution of devices to study sites
- Develop device and application user guides and troubleshoot issues by working with sites/sponsors, as necessary
- Create study and application specific documents to support regulatory submissions and approval
- Monitor data entry for quality and report compliance metrics to Sponsors (e.g., monitoring how well patients are completing forms, identifying and flagging data for errors, etc.)
- Other assigned projects and tasks
Qualifications:
- Bachelor’s degree in a health related field with strong attention to detail and working knowledge of Excel and Word;
- Knowledge of medical terminology;
- 1-2 years of experience in a pharmaceutical or CRO setting preferred.