Lavori attuali relativi a Clinical Research Associate II - Milano, Lombardia - Allucent

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    Job Title: Clinical Research Associate IIAbout the Role:We are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a Clinical Research Associate II, you will play a critical role in the success of our clinical trials by ensuring that all study activities are conducted in accordance with Good Clinical Practice (GCP),...

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    2 settimane fa

    Milano, Lombardia, Italia Allucent A tempo pieno

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    Milano, Lombardia, Italia Psi Cro Ag A tempo pieno

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    Milano, Lombardia, Italia Tn Italy A tempo pieno

    Job Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a CRA II, you will play a critical role in ensuring the successful execution of clinical trials.Key Responsibilities:Monitor investigation sites to ensure compliance with study protocols and regulatory requirements.Perform...

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    Milano, Lombardia, Italia PSI A tempo pieno

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    Milano, Lombardia, Italia PSI CRO A tempo pieno

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    4 settimane fa

    Milano, Lombardia, Italia Pharmiweb A tempo pieno

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  • Clinical Research Associate II

    3 settimane fa

    Milano, Lombardia, Italia Psi Cro Ag A tempo pieno

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  • Clinical Research Associate II

    1 mese fa

    Milano, Lombardia, Italia Allucent A tempo pieno

    Job Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.Key Responsibilities:Monitor and control investigation sites to ensure compliance with trial...

Clinical Research Associate II

2 mesi fa

Milano, Lombardia, Italia Allucent A tempo pieno
About the Role

We are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.

Key Responsibilities
  • Monitor and control investigation sites to ensure compliance with trial protocols and regulatory requirements.
  • Perform site initiation, monitoring, and closure visits to ensure data quality and integrity.
  • Track and supervise the collection of study data to ensure timely and accurate reporting.
  • Review and collect regulatory documents as required.
  • Prepare and submit site visit reports and telephone contact reports.
  • Maintain and update the Clinical Trial Management System (CTMS) in accordance with SOPs and study-specific directives.
  • Act as the main point of contact between the project team and site staff.
  • Collaborate with the Centralized Monitoring Team to evaluate risk-based monitoring activities and prevent issues.
  • Identify and resolve site issues, including recruitment challenges and IP shipment status.
Requirements
  • At least 2 years of experience in clinical research.
  • Strong therapeutic background and knowledge of clinical trials.
  • Ability to travel for up to 8 days per month, depending on project needs.
  • Excellent communication and project management skills.
  • Mature management skills, with the ability to define and meet project requirements.
  • Proven organizational abilities and excellent written and oral communication skills.
What We Offer
  • Comprehensive benefits package.
  • Competitive salary.
  • Departmental study/training budget for furthering professional development.
  • Flexible working hours.
  • Opportunity for remote/hybrid working.
  • Leadership and mentoring opportunities.
  • Participation in our Buddy Program.
  • Internal growth opportunities and career progression.
  • Financially rewarding internal employee referral program.
  • Access to online soft-skills and technical training.