Cra, Italy

1 settimana fa

Milano, Italia Proclinical A tempo pieno

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.

***

**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 1-2 years of experience in pertinent work and training.
- Past involvement in oncology would be ideal, and in a supervisory role.
- Know-how 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 60-80% 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.

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