Senior II Clinical Research Associate / Attaché de Recherche Clinique - Global CRO

Work model: Remote

Locations: Italy

Are you willing to take your career to the next level in a market-leading global CRO, with a wider range of projects to learn from?

As an experienced Senior II Clinical Research Associate, you could be looking to broaden your therapeutic, geographic, and study exposure, or perhaps for a future beyond monitoring thanks to this market-leading CRO's development opportunities. Within this CRO, you’ll benefit from training and development programs to evolve within your role and career and progress in the direction you choose, as they do not believe in a ‘career ceiling.’

WHAT'S IN IT FOR YOU?
• Working with global sponsors on international projects.
• Focus on quality, not quantity! They invest in keeping their teams stable with consistent workloads.
• The chance to work on cutting-edge medicines right at the forefront of drug development.
• Genuine career development... opportunities for those who want to grow as part of the organization.
• Flexible conditions and an attractive remuneration package.
• Office or home-based roles available.

REQUIRED FOR THE ROLE/INCLUDED:
• At least 2-3 years of independent monitoring experience onsite.
• 6-8 visits per month on average.
• Home allowance and internet available.

RESPONSIBILITIES
• Perform site selection, initiation, monitoring, and close-out visits.
• Work with sites to adapt, drive and track subject recruitment plans.
• Administer protocol and related study training to assigned sites and establish regular lines of communication.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations – escalating quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans.

SKILLS REQUIRED
• Bachelor's degree in healthcare or another related field, or educational equivalent.
• Minimum 2-3 years of independent on-site monitoring experience.
• In-depth knowledge and skill in applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• In-depth therapeutic and protocol knowledge as provided in-company training.
• Excellent organizational, problem-solving, and time-management skills.
• Strong written and verbal communication skills in English and Italian.

Interviews are already being conducted and this opportunity won't be available for long, apply now!

Does the above sound like you? Then click apply and send over your CV/any questions to [email protected] or call (+44) 20 3019 5999
Italy

Salary Criteria