Patient Service Specialist

1 month ago


Philadelphia, United States Blue Ocean Full time

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 study-related documents, i. Including DOA log, source documents, CRFs, AE forms, enrollment log, training log, correspondence, etc.
- Proper reporting of serios and non-serious 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 close-out 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:

- In-person

**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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