Cta/ctc

Description

Qualification
Support of clinical grants tasks: - Review study budgets/clinical trial agreements for consistency with study protocol - Updating of clinical and study planning databases Review study budgets/clinical trial agreements for consistency with study protocol
ABC (anti-bribery + corruption checks) on all HCP (fact finding, workflows, tracking, renewals) + troubleshooting with compliance, technical services etc. - Clinical trial payments and payment tracking
Financial disclosure (check need, track, process letters and documentation)
Denied parties screening (DPS) - Compliance checks
Disclosure agreements: Generate and track Trial master file reconciliation of clinical grants/compliance documents - Maintenance of trackers
GMS (grants management system): enter and track payments, run reports execute payments in COMET (SAP), purchase orders as needed Requirements:
Advanced communication skills (written and verbal) in local languages and English
- Understanding and knowledge of study protocols and study working documents, lab manuals, etc
Good understanding of the clinical research processes
Understanding of the ICH/GCP (international good clinical practice guidelines and harmonization) and local clinical trial regulations - Number of years of experience targeted: Junior - Degree: Bachelor degree (e.g. medical assistant, or paramedical education) or relevant

Seniority Level
Entry level
Industry
Pharmaceuticals

Employment Type
Full-time
Job Functions

Pay: €20,000.00 - €35,000.00 per month

Schedule:

- Day shift