Patient Service Specialist - Philadelphia, United States - Blue Ocean
Description
Weekly coordination of multiple investigator-initiated research and clinical trial focused in Head and Neck Cancer. Screen, recruit, and consent potential study participants as specified per protocol.- Collect blood and other specimens and coordinate specimen storage and processing with various labs.
- Complete CRFs and data entry to study databases, sample process and shipping, patient reimbursement, research billing review, etc.
- Coordinate the administration of the investigational product and study related medications including obtaining orders, collection of data from source documents pertaining to study visits and transcribe to case report form, including concomitant medications and adverse events.
- Maintain all studyrelated documents, i. Including DOA log, source documents, CRFs, AE forms, enrollment log, training log, correspondence, etc.
- Proper reporting of serios and nonserious adverse events to the study team.
- Prepare and participate in the conduct of audits by the study sponsors, CROs, the FDA, and other entities as required.
- Conduct initiation, monitoring, and closeout visits with sponsors and/or CROs.
- Maintain records of monthly/yearly progress reports, generate meeting agenda, record and distribution of meeting minutes, assist with IRB, CTSRMC, or other regulatory submissions.
- Other duties and responsibilities as assigned.
Job Types:
Full-time, Contract
Pay:
From $50,000.00 per year
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Work setting:
- Inperson
Education:
- Bachelor's (preferred)
Experience:
- Patient service: 1 year (preferred)
- Patient assessment: 1 year (preferred)
- Medical collection: 1 year (preferred)
Work Location:
In person
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