Clinical Research Coordinator

Actalent; Toscana; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading CRO is seeking a Clinical Research Coordinator in Florence, Italy. This role involves coordinating trials and engaging with patients on-site, requiring a minimum of 2 years of clinical research experience. Candidates should have proficiency in data entry using EDC systems. This position offers an exciting opportunity to gain valuable industry experience and is positioned on-site, necessitating local availability in Florence.

Competenze

• Minimum 2 years experience in clinical research.
• Ability to work independently and as part of a team.
• Experience with patient activities within trials.

Mansioni

• Coordinate clinical trials and patient activity on site.
• Ensure data entry is accurate using EDC platforms.

Conoscenze

Data entry

Clinical research experience

Descrizione del lavoro

A leading CRO are looking for a Clinical Research Coordinator in Florence, Italy.

This is an exciting opportunity with candidates to start as soon as possible and great opportunity to gain industry experience.

The Clinical Research Coordinator must have minimum 2 year clinical research experience as the CRO need an individual who can work independently as well as part of a team. Day to day responsibilities will involve a lot of patient activity within the trials on site.

This will be an onsite role so the candidate will need to based in Florence.

Experience

• Minimum 2 years experience in clinical research
• Data entry using EDC (IMedidata, RAVE, Redcap etc)