Job Title: Clinical Data Associate
Type: 1 year contract (Benefits Available)
Location: Fully Remote
The team is seeking a highly motivated individual to join their Clinical Data Associate. You will be responsible for overseeing all aspects of external data management for the clinical development programs with guidance from the Manager, CDM.
Responsibilities (include but are not limited to):
- Assists in implementing routine activities involving CDM interaction with other study management team members.
- Identifies, tracks, and resolves routine queries and issues.
- Demonstrates ability to identify problems early and communicate escalation issues appropriately.
- Project level coordination and day to day oversight of External Data Management tasks
- Manage data management timelines to ensure goals of teams are met
- Manage vendors, and ensure appropriate resources are available to meet the demands of the assigned clinical trials
- Provide CDM expertise for external vendor data coordination, collection, and cleaning to efficiently ensure high quality data
- Manage CDM deliverables in coordination with internal and external cross functional teams.
- Review clinical data on an ongoing basis to ensure quality data
- Create Data Transfer Plans and other pertinent External Data documentation review, query management, report delivery to study teams, study timeline and database snapshot coordination for analysis including Safety Review Team, Interim Analysis, etc.
- Flexible to changing priorities, detail-oriented, works well under pressure and able to take on unfamiliar tasks.
Requirements:
- 3 years of experience and a BS degree (or equivalent experience)
- 1 years of experience and a MS degree or PhD (or equivalent experience)
- Scientific background and experience with lab data handling
- Excellent verbal and written communication skills, including the ability to clearly describe critical technical CDM aspects to non-CDM staff
