Clinical Research Associate - Paris
- Employer
- Labcorp
- Location
- Paris, France
- Salary
- Competitive
- Start date
- 27 Aug 2019
- Closing date
- 26 Sep 2019
View more
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
This is the chance to join our CRO and a dynamic and supportive team!
Responsibilites:
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study 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 legal department with statements of agreements as assigned
- Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
- Audit follow-up
What makes this job special?
- Career progression will be exceptional because there are lots of studies coming through in 2019 across a variety of therapeutic areas
- You will be 100% client focused with a prestigious Pharmaceutical company
- Your Line Manager will be based in the Paris area too, there to support you where you need it
Other Information:This role is a full time & permanent position to be employed through Covance. For more information please contact Gerda Quenum at gerda.quenum@covance.com.
Education/Qualifications:
- Scientific University degree
- CRA training certificate desirable (SupSanté, Clinact, ILV...)
- Valuable Clinical Monitoring experience.
- Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Experience with site audits
- Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
- Good planning, organization and problem solving abilities
- Ability to work with minimal supervision
- Good communication and interpersonal skills
- Good analytical and negotiation skills
If you are looking to broaden your therapeutic expertise whilst gaining exposure to a Pharmaceutical working environment this is a fantastic opportunity to seize now!
We are looking forward to hearing from you and welcoming you to Covance!
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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