Skip to main content

This job has expired

Clinical Project Assistant - sponsor-dedicated - Paris

Employer
Labcorp
Location
Paris, France
Salary
Competitive
Start date
19 Oct 2021
Closing date
17 Nov 2021

View more

Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Send job

Job Details


Clinical Project Assistant - sponsor-dedicated - Paris

Location: Paris, France

A formula for clinical innovation: Labcorp Drug Development. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 60,000 employees advance life-changing medicines across a wide range of therapeutic areas - improving health and lives every day.

If you are looking for a position in which you can leverage your organizational skills and your clinical expertise as much as your talent to connect and communicate with a wide variety of people, this is the perfect opportunity! Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

What you can expect from us:
  • flexible working hours, capped overtime and compensatory time off in lieu
  • permanent employment contract with Labcorp Drug Development
  • travel time = work time
  • highly competitive compensation packages
  • subsidized meals and transportation allowances
  • bonus schemes / profit sharing
  • regular, merit-based salary adjustments
  • significant employer contribution to an attractive pension scheme
  • extensive insurance coverage, including medical, life, short as well as permanent disability and accidents
  • excellent training and career development opportunites as well as support with furthering your education
  • strong support from Line Management and more than 20'000 colleagues worldwide
  • the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years


Your responsibilities:
  • Support project teams in the full spectrum of clinical research activities such as study start up, site management / closure, document management (eTMF and paper-based), regulatory and site start-up responsibilities, meeting planning
  • Coordinate internal and external stakeholders, facilitating smooth processes and top quality
  • Administrative support of various contract teams including approvals, quality assurance and document management (contract databases and / or paper-based)
  • Set up and maintain clinical investigator files and documentation
  • Prepare investigator budget payments and tracking systems; generate tracking reports
  • Enter and maintain data into selected study tracking databases and ensure a high level of data quality
  • Prepare monitoring visit documentation for CRAs, Project Managers etc.
  • Oversee appropriate archiving of study documents and other materials
Education/Qualifications:
  • Degree or completed vocational training (office management, administration, health care, life science or similar preferred) or equivalent professional experience
Experience:
  • First experience in a comparable role including familiarity with submission / study start up processes
  • Familiarity with French as well as international regulations around clinical trials (ICH, GCP etc.) and the French regulatory authorities
  • Proficient user of IT applications such as MS Office (including strong MS Excel skills) and clinical IT applications (e.g. Veeva Vault)
  • Strong organizational and project management skills with a keen attention to detail and a high sense of accountability
  • Excellent communication skills in business fluent French and English - verbal and written - and strong interpersonal skills are a must


#LI-AR1

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.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
 Maidenhead
SL6 3QH
United Kingdom
Send job

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert