Cra, Germany - Munich, Deutschland - Proclinical
Beschreibung
Proclinical are recruiting a CRA, Germany for a CRO. This role is on a permanent basis with the ability to work remotely from anywhere in Germany.Responsibilities:
- Examine the clinical research site's patient recruitment and retention success as well as provide recommendations for improvement.
- Accomplish supervising reports and followup letters, which involves offering summaries of the significant discoveries, aberrations, deficiencies and suggest actions to secure compliance.
- You will manage medical device and/or investigational product/drug responsibility as well as inventory.
- Verify and evaluate adverse events, serious adverse events, concomitant medications and consistent illnesses to confirm precise data reporting rendering to the protocol.
- Perform qualification instigation, supervision and closeout visits for research sites in compliance to the approved protocol.
- Other duties may be assigned to this role.
Key Skills and Requirements:
- Educated to a degree level in a health science or life science discipline.
- At least 1.5 years of experience in a CRA role.
- Willing to travel around Germany, Austria and Switzerland for business needs up to 6080% of the time.
- Computer literacy.
- Presentation and communication skills both verbally and in writing.
- A high attention to detail with the ability to manage time efficiently.
- Fluency in the English and German languages.
- Demonstrated familiarity with clinical patient management, protocol, CRF, preparing ISF, documentation to be proposed to competent authorities.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
LI-LS3
CRODelivery
Clinical
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