Cra, Italy - Milano, Italia - Proclinical

Proclinical

Azienda verificata

Milano, Italia

2 settimane fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

Proclinical are recruiting a CRA, Italy for a CRO. This role is on a permanent basis with the ability to work remotely from anywhere in Italy.

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Responsibilities:

Gather and evaluate site necessary documents and guarantee site regulatory files are accomplished and precise.
Supervise site compliance with IRB policies/procedures and assure reporting, proposals and approvals in a timely manner.
You will track and report progression of study, data supervising, protocol variations, issue resolution, and follow up compliance.
Plan and accomplish visit trip reports, confirmation and follow up letters in timelines defined in the CMP.
Evaluate research specimen sample documentation, storage and processing, and guarantee shipments are sent to central lab when needed.
Other duties may be assigned to this role.

Key Skills and Requirements:

Educated to a degree level or at least 12 years of experience in pertinent work and training.
Past involvement in oncology would be ideal, and in a supervisory role.
Knowhow of and capable of implementing CFR and GCP/ICH.
Familiarity within international clinical trials.
Computer literacy.
An organised individual with the ability to manage own time efficiently.
Capable of handling various tasks simultaneously with the ability to take own initiative.
Able to prioritise workload with a high attention to detail.
Interpersonal and communication skills both verbally and in writing.
Willing to travel for business needs up to 6080% of the time.
Works well in a team.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

LI-GE1

CRODelivery

Clinical