Senior Cra

5 giorni fa


Ancona, Italia Teleflex A tempo pieno

A global medical device company is hiring a Senior Clinical Research Associate responsible for conducting and scheduling monitoring visits to ensure compliance with regulations and internal standards.The ideal candidate has over 5 years of clinical trial monitoring experience, excellent communication skills, and a bachelor's degree in life sciences.This role requires fluency in both Italian and English, alongside significant travel commitments.This position offers the opportunity to work independently and contribute to high-quality clinical research efforts.#J-*****-Ljbffr



  • Ancona, Italia Altro A tempo pieno

    Social network you want to login/join with:Senior Clinical Research Associate, ancona col-narrow-leftClient: TeleflexLocation: Job Category: Other-EU work permit required: Yescol-narrow-rightJob Reference: Job Views: 2Posted: Expiry Date: col-wideJob Description: POSITION SUMMARY :The Senior Clinical Research Associate (Senior CRA) is responsible for...


  • Ancona, Italia Jr Italy A tempo pieno

    Social network you want to login/join with:Senior Clinical Research Associate, anconacol-narrow-leftClient:TeleflexLocation:Job Category:Other-EU work permit required:Yescol-narrow-rightJob Reference:Job Views:2Posted:Expiry Date:col-wideJob Description:POSITION SUMMARY:The Senior Clinical Research Associate (Senior CRA) is responsible for scheduling and...


  • Ancona, Italia JR Italy A tempo pieno

    Social network you want to login/join with: Senior Clinical Research Associate, ancona col-narrow-left Client: Teleflex Location: Job Category: Other - EU work permit required: Yes col-narrow-right Job Reference: Job Views: 2 Posted: Expiry Date: col-wide Job Description: POSITION SUMMARY : The Senior Clinical Research Associate (Senior CRA) is responsible...

  • Senior CRA: Trials

    3 settimane fa


    Ancona, Italia JR Italy A tempo pieno

    A leading medical device company is seeking a Senior Clinical Research Associate to conduct on-site and remote monitoring visits. The ideal candidate has at least 5 years of experience in clinical trials and a strong knowledge of regulatory compliance. You will work closely with investigators to ensure accurate data collection and adherence to protocols, all...