Clinical Research Associate - Clinical Operations

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Job description

Covance is now Labcorp, and we are much more than a normal CRO.

We were named to * Fast Company magazine's list of 2021 Most Innovative Companies * for its leadership in scientific innovation in the fight against COVID-19. Labcorps Drug Development Business, Covance, was recognized with the *2020 Global CRO Company of the Year Award* by Frost & Sullivan for our capacity to integrate digital technologies, remote monitoring, and telemedicine services to ensure continuity of and decentralizing clinical trials.

We have supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today.

Join us and see why Covance are uniquely positioned to offer you not only a job, but a stable, long-term international career, and why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

* THE CRA JOB *

Remote jobs in the North of Italy: Milan, Rome, Bolognia, Naples. Locations well connected by airport/train.

These jobs would suit CRAs who already have minimum *1 years* independent clinical monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) in Italy, with international ph I-III clinical trials, within pharma or CRO environment.

* IS THIS YOU? *

At Covance we trust our CRAs and so we will give you autonomy to organize your work. In turn, we expect you to go beyond the typical CRA role and really be an expert of your protocol and to own your sites .

* Your focus will be direct site management and we expect you to influence site performance

* We need your hands-on experience nurturing a collaborative relationship with your sites: how will you make the study relevant for them? How will you efficiently solve their issues or build their audit-ready habits?

Covance has invested in creating a strong IHCRA network who will be your support with admin tasks, payments, solving queries, issues with vendors or site staff training... freeing you to be focused on the clinical side.

APPLY NOW

... so we can tell you about the team support that permeate everything we do, how our managers constantly review study/site allocation to ensure workload balance or why you will not grow a stale career with us because you can choose between therapeutic areas, types of clients, etc.

Education/Qualifications:
* University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology
* Thorough knowledge of ICH Guidelines and GCP
* Fluent in Italian and in English, both written and verbal
Experience:
Clinical monitoring in Oncology studies ph I to III is a strong positive.

Excellent understanding of Serious Adverse Event (SAE) reporting

Minimum of three 1 year of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)

Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs