Cra I / Ii - Oncology Focus Milano

Cra I / Ii - Oncology Focus
Milano
Lombardia, Milano

Competitive

- Milan, Italy

- Permanent

**CRA I / II - Oncology focus - 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 a CRA I or II, you could be looking to broaden your therapeutic, geographic, and study exposure, allowing you to improve your overall skills and knowledge for future progression towards Senior CRAs positions, 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.

**WHAT'S IN IT FOR YOU?

- Focus on complex Oncology projects.

- Working with global sponsors on international projects.

- Focus on quality, not quantity!

They invest in keeping their teams stable with consistent workloads.

- Genuine career development opportunities for high performers.

- Flexible conditions and an attractive remuneration package.

**REQUIRED FOR THE ROLE/INCLUDED**:

- 1+ year of independent monitoring experience.

- 6-8 visits per month on average.

- Average of 2-3 protocols at once.

- Home allowance and internet available.

**RESPONSIBILITIES

- Perform site selection, initiation, monitoring, and close-out visits.

- 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 1+ 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.

- Strong written and verbal communication skills in English and French.