Location: Cork, Ireland (relocation package available)
The Trial Capabilities Associate provides clinical trial capabilities in support of clinical development. The associate is accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and close-out. The associate is responsible for obtaining clinical trial authorizations and ethical approvals and activities related to records management and site training. The associate will ensure inspection readiness through a complete, accurate and readily available Trial Master File.
Clinical Trial Responsibilities
Minimum Qualification Requirements:
Location: Cork, Ireland ( Relocation package available) The Contract and Budget Associate is responsible for overseeing specific clinical contract and...Apply For This Job
Trial Master File Analyst – native French speaker Our client, a multinational pharmaceutical company is looking for a French speaker...Apply For This Job