Clinical Research Associate

1 mese fa

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

We are seeking a highly skilled and experienced Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for ensuring the smooth execution of clinical trials, from site initiation to close-out.

Key Responsibilities
  • Monitor and manage clinical trial sites to ensure compliance with Good Clinical Practice (GCP), International Conference on Harmonisation (ICH), and applicable regulations.
  • Conduct site initiation, monitoring, and close-out visits to ensure trial protocols are followed and data is accurately collected.
  • Collaborate with cross-functional teams, including project management, clinical operations, and regulatory affairs, to ensure trial timelines are met and quality standards are maintained.
  • Develop and maintain strong relationships with site staff, investigators, and other stakeholders to ensure effective communication and issue resolution.
  • Identify and mitigate potential risks and issues, and develop contingency plans to ensure trial continuity.
  • Ensure accurate and timely data collection, and maintain high-quality documentation throughout the trial.
  • Participate in training and development activities to enhance clinical trial knowledge and skills.
Requirements
  • At least three years of clinical research experience, with a strong background in clinical trial monitoring and management.
  • Relevant life science degree or healthcare background, with a strong understanding of medical terminology and clinical trial processes.
  • Excellent communication, interpersonal, and organizational skills, with the ability to work effectively in a fast-paced environment.
  • Strong analytical and problem-solving skills, with the ability to identify and mitigate potential risks and issues.
  • Proficiency in computer applications, including Microsoft Office and clinical trial management systems.
What We Offer
  • A comprehensive benefits package, including competitive salary, health insurance, and retirement plan.
  • Opportunities for professional growth and development, including training and mentorship programs.
  • A dynamic and collaborative work environment, with a team of experienced professionals dedicated to delivering high-quality clinical trials.
  • The chance to work on a wide range of clinical trials, from small to large-scale studies, and contribute to the development of new treatments and therapies.

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