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Paris, FRA JOBS - Covance

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Local CPM / France (Location: 92) Paris, FRA

. . . Pro-actively drives/tracks execution and performance of deliverables/timelines/results to meet country commitments for assigned protocols and forecasts country resource needs * Responsible for quality and compliance in assigned protocols in country. Oversees CRAs and Coordinators on assigned projects. Oversees training compliance. Performs quality control visits. Reviews Monitoring Visits ReportsRead More

Home-Based Sr. CRA Oncology / Paris region Paris, FRA

. . .tigious Pharmaceutical company. * Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit' targets * The job is permanent and full time * Your Line Manager will be based in France, possibly in your region * You will be joining a big team with a well organised structure and robust processes in place As an Experience d Sr.CRA you'll be involved in initiation, routine & clRead More

Medical Director , US Paris, FRA

. . .rkplace, along with access to comprehensive benefits. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning. Our mission is to help our clients bring the miracles of Read More

Medical Director , US Paris, FRA

. . .rkplace, along with access to comprehensive benefits. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning. Our mission is to help our clients bring the miracles of Read More

Site Study Liaison Paris, FRA

. . .primary purpose of the successful candidate would be site engagement. Within the EMEA region you will be positioned to face our Client's customers and drive recruitment. Home based in FRANCE you would be assigned to critical studies with a clear remit of engaging customers with tasks including: PI focused site visits – to communicate key study messages and address barriers to recruitment. Site Read More

Clinical Team Lead Paris, FRA

. . .ole is essential. Primary duties: * Responsible and accountable for the management of the clinical study team with particular emphasis on teamwork, quality, timelines, budget, metrics and compliance with the project plans and SOPs. * Develop the strategy, plans, tools and training to oversee and assess performance of the clinical team, in the conduct and compliance of site visits (on site and reRead More

Project Manager, OES Paris, FRA

. . .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

Manager Regulatory Submissions - Flexible location within EMEA Paris, FRA

. . .ce tasks. This position is responsible for the management of a team of regulatory professionals and/or responsible for timely preparation/coordination of regulatory submissions for a particular project and must work to high standards (governmental, Sponsor, Covance and self) with minimal supervision. It is the responsibility of this position to ensure that documents are prepared to the required sRead More

Medical Writer II-CDS Paris, FRA

. . .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

Clinical Research Associate Paris, FRA

. . .tudy files, conduct of pre-study and initiation * Prepare accurate and timely trip reports * Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor * Negotiate study budgets with potential investigators and assist the Covance legaRead More

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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 www.gettinghired.com 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).