Summary
Join our team as a Pre-Screening Lab Process Coordinator and help facilitate oversight of lab result process for Care Access's Pre-Screening Program.
Requirements
- Fluent reading and writing in Portuguese
- 1 year of Clinical Research experience, clinical research laboratory experience is a plus
- Strong knowledge of GCP-ICH requirements and data collection in a research setting
Responsibilities
- Coordinate with clinical and administrative staff, and management to ensure that all necessary labs are returned to the proper party
- Ensure that all lab results are accurately recorded, filed in the appropriate participantβs medical record, and communicated with the Retention Team
- Escalate abnormal lab results to the appropriate medical personnel and ensure proper medical oversight is maintained
- Communicate with Care Access and vendor laboratories to ensure samples have properly resulted
- Perform checks of participant data in tech systems to ensure accurate lab reporting
- Effectively perform quality checks of teammatesβ work to ensure the highest level of data quality
- Maintain a call schedule with lab process manager for communicating needs such as medical oversight and cross functional collaboration
- Perform duties of the role in compliance with state specific guidelines, legal, regulatory, and organizational policies
Benefits
- PTO/vacation days, sick days, holidays
- 100% paid medical, dental, and vision Insurance. 75% for dependents
- HSA plan
- Short-term disability, long-term disability, and life Insurance
- Culture of growth and equality
- 401k retirement plan