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Clinical Research Associate - all level of experience

Employer
Labcorp
Location
Rueil-Malmaison, France
Salary
Competitive
Start date
21 Nov 2022
Closing date
20 Dec 2022

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

Job Details

Get ready to redefine what's possible and discover your extraordinary potential at Labcorp Drug Development. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. 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.

Join Labcorp! Join the Pursuit!

What you can expect from us:
  • flexible working hours, capped overtime and compensatory time off in lieu
  • 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 opportunities 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:
  • Own all aspects of site management as described in the project plans.
  • Ensure the study staff conducting the protocol receive all materials and instructions to safely enter patients into the study.
  • Protect study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by diligently reviewing source documents. Monitor data for missing or implausible entries.
  • Perform the required monitoring tasks in an efficient manner, according to SOPs and established guidelines; submit accurate and timely trip reports.
  • Review progress of projects and initiate appropriate actions to achieve target objectives.
  • Act as a primary contact for clinical trial suppliers and other vendors.
  • Own the entire process of Serious Adverse Event (SAE) reporting
  • Generate queries and resolve issues according to data review guidelines on Labcorp or sponsor data management systems


Education:
  • Degree in a relevant field such as life sciences, biology, health care (management), nursing, pharmacology, (veterinarian) medicine, etc.
  • In lieu of the above, a valid certification in health / life sciences by an accredited institute


Experience:
  • Solid independent monitoring experience in France as CRA, with a focus on complex clinical trials (phases II and III)
  • Proven experience in a variety of therapeutic areas, preferably including oncology
  • Awareness of applicable clinical research regulatory requirements such as local regulations, GCP / ICH and the French regulatory authorities landscape
  • IT-literate, including Microsoft Word, Excel, PowerPoint, and preferably eTMF solutions such as Veeva Vault
  • Effective time management and organizational skills and a keen attention to detail
  • Ability to establish and maintain effective, trustful working relationships with internal and external stakeholders
  • Excellent communication skills in both French and English - spoken and written - are a must


Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement .

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

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