Oncology Clinical Research Coordinator

hace 5 días

La BarcelonetaBarcelona, España RapidTrials A tiempo completo

***:
An excellent opportunity for an experienced oncology clinical research coordinator (CRC) looking for a part-time freelance position with some on-site and some remote work, The CRC will support the Principal Investigator (“PI”) and research team with implementing an industry-sponsored Phase 2 Oncology study.

This position requires the following time commitment and availability:
**Location**: **Zaragoza and remote. **Note this is a hybrid position. Some tasks can be performed remotely, such as communications and data entry (the CRC will have remote access to the electronic medical records). Some tasks require on-site - estimate 1 day per week on-site.

**Hours**: 20 hours per week

**Duration**: 15 months

**Type**: Free Lance/Consultant

**Hours/month**:85

**POSITION KEY ACCOUNTABILITIES**:

- .
- Coordinate and work with site study personnel to ensure all study procedures are completed according to the protocol requirements and timelines
- Coordinate and support communication between site and CRA
- Maintenance of Investigator Site File
- Collection of study documents and required signatures, including but not limited to CV, GCP
- Data entry from source documents to Electronic Data Capture Forms (EDC)
- Review and QA data entry
- Responds to and resolves data queries
- Potentially contact with the patient regarding scheduling and rescheduling Principal Investigator (PI) visits (note the PI and Sub-Investigator complete all visits)
- Communicates with PI to ensure review of data and patient labs on a timely basis
- Other duties as assigned by PI

**EXPERIENCE/REQUIREMENTS**
- Minimum two years previous industry-sponsored clinical research experience as an Oncology Clinical Research Coordinator
- CRC certification (preferred)
- Speaks and writes Spanish at the “Professional Level” or higher
- Speaks and writes English at the “Professional Level” or higher
- For applicants that are not Spanish citizens - appropriate visas must be in place before interviewing for the position (no sponsorship is available)
- Currently lives near the site in Zaragoza and able to reliably commute to the site

**ONBOARDING**
- Complete protocol, Investigational Product, CRF and required site-specific SOP training
- Evidence of being fully vaccinated for the following: COVID 19 Vaccine
- Certificate of completion for GCP/ICH Training

**START DATE: ASAP**

**INTERESTED CANDIDATES**

Forward their resumes along with compensation requirements and references

**Job Types**: Part-time, Contract
Contract length: 15 months
Part-time hours: 20 per week

Pay: Up to 65.00€ per hour

COVID-19 considerations:
Evidence of being fully vaccinated for the following: COVID-19 Vaccine

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