16231-clin Data Coord

Job Overview
Serve as Data Operations Coordinator (DOC) for one or two global studies with fewer than 10 operations staff (excludes DE), or serve in a leadership role to a specific DM Task.

Essential Functions
- Manage delivery of projects through full data management study life-cycle (with mínimal guidance).
- With guidance from DTL or Manager, manage project timelines and quality.
- Determine resource needs.
- Identify out-of-scope work.
- Serve as Data Operations Coordinator or Data Team Lead (with guidance).
- Perform comprehensive data management tasks including data review, writing and resolving data clarifications.
- Perform database designer activities for technologies not requiring extensive programming.
- Perform comprehensive quality control procedures.
- Independently bring project solutions to the CDM team.
- Solve issues through using the global issue escalation/communication plan.
- Consult with Standards Group for process issues.
- Communicate ideas for process improvement.
- Assist in developing and implementing new technology.
- Understand and comply with core operating procedures and working instructions.
- Meet objectives as assigned.
- Develop and maintain good communications and working relationships with CDM team.
- Interact with CDM team members to negotiate timelines and responsibilities.

**Qualifications**:

- Bachelor's Degree Health, clinical, biological sciences, or related field Req
- 1 year clinical trials experience in function similar to DM; or equivalent combination of education, training and experience Req
- Good understanding of clinical drug development process. Intermediate
- Background in medical terminology, Pharmacology, Anatomy, and Physiology. Intermediate
- Excellent organizational, communication, and data management skills (detailed oriented). Intermediate
- Ability to establish and maintain effective working relationships with coworkers, managers and clients. Intermediate