To us it’s personal.

Milan, ITA JOBS - Covance

Start-up Specialist II Milan, ITA

. . . Specialists will: Act as the lead contact with investigative sites during assigned site start-up activities. Oversee timely collection of the required investigator and regulatory documents for a study as specified by regulatory authorities and sponsor. Ensure the ongoing accuracy and quality of site/study documents. Ensure high quality documents are filed in (e)TMF and systems are updated on an Read More

Project Manager, OES Milan, ITA

. . .ing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met. The Senior Project Manager is expected to have a working knowledge of drug development and clinical study execution in the Interventional Post Market and Observational study arena. They alsoRead More

Medical Writer II-CDS Milan, ITA

. . .on level documents under guidance of senior staff. * Production of scientific publications and other documents (e.g., abstracts, posters, manuscripts, etc.). * Interpretation of clinical, pharmacokinetic, pharmacodynamic and statistical results as appropriate. * Lead and coordinates activities of other writers on higher complexity narrative projects. * Ensure timely delivery of high quality documeRead More

Senior Clinical Operations Manager (line management) Milan, ITA

. . .nagement and Development (PMD), Individual Development Plan (IDP), Line of Sight Goals and “Shoves & Tugs” * Responsible for appropriate management and resolution of performance issues * Develop and measure performance indicators for assigned staff within Clinical Operations. * Identify individual training needs and assist with the coordination and conduct of training and development efforts, regiRead More


. . .oject Management organization is strong in Europe: 200+ PMs. The Covance´s Oncology PM team offers unique opportunities to gain exposure across a broad clinical trial portfolio. Whether your ambition is to work at the forefront of innovative clinical trial design or play a pivotal role in leading and coordinating global clinical trials in Big Pharma, we have the right job for you. WHAT MAKES THISRead More

Clinical Team Lead, Medical Devices and Diagnistics Milan, ITA

. . .MEA (office or homebased options). You will be managing clinical medical device studies, and leading CRA activity across multiple countries. Previous Experience in a similar role is essential. Primary duties: * Responsible and accountable for the management of the Medical Device clinical study team with particular emphasis on teamwork, quality, timelines, budget, metrics and compliance with theRead More

CRA Junior/Bench - Sponsor Dedicated Milan, ITA

. . .erence in the lives of millions of people… and you will too. If your aspiration is starting a job within clinical trials, think long-term and the possibilities we can offer you: * We have helped the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today and * 100 % of all Oncology drugs approved in 2016. ExplorRead More

Clinical Sr Auditor QA&C - EMEA (home based or office based) Milan, ITA

. . .egulations and guidelines, and fulfill client and Covance requirements. The main responsabilities are: * Leads audit teams in the conduct, reporting an follow up of regional and local QA audits, ensuring compliance to applicable SOP, Master Audit Plan, and within specified timeframe and quality standards * Conducts complex, directed and /or time sensitive audits * Participates in global QA auditRead More

Project Manager/Senior Project Manager - Medical Devices Milan, ITA

. . .e any combination of the following: single or limited services study or a small regional cross−functional study. Furthermore, a Senior Project Manager may also manage a portion of a larger global study within a given geographical region (i.e. North America, Western Europe, etc.) Duties & Responsibilities * Manage, lead and motivate cross-functional project teams, facilitating the team's ability Read More

CRA II or Senior CRA (home based or office based) Milan, ITA

. . . CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit' targets (6 per month) * The role can be home based or office based in Italy. * Join a stable team of CRAs and benefit from outstanding training and development, both initially and throughout your career * Join a company where people tend to stay for 6-10 years rather than 1-3! * Join a genuinely friendly and supportive companRead More


Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).