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Clinical Research Associate (CRA) - Madrid

Employer
Labcorp
Location
Madrid, Spain
Salary
Competitive
Start date
11 Aug 2022
Closing date
8 Sep 2022

View more

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

Job Details

Labcorp Drug Development are helping to develop what could be the first pharmacological treatment able to help 3+ million severily ill hospitalized patients worldwide... and we need you to contribute with your expertise .

Labcorp Drug Development

With all the uncertainty in the world, your job stability should not be a concern.

Labcorp have supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. But we are much more than a normal CRO:

  • We are also the world's biggest Central Lab, generating more clinical trial data than all other central laboratories combined
  • Our Early Phase Solutions have proved to shave off 30 % time from lead candidate to Proof of Concept
  • LabCorp were the first in receiving FDA approval to perform COVID19 tests using an at-home collection kit.


Join us and see why Labcorp Drug Development are uniquely positioned to offer you not only a job, but a stable, long-term international career, and why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

What we have to offer:
  • work as part of a diverse and stable team
  • in-depth onboarding, including personal support from your mentor
  • flexible working hours and compensatory time off in lieu
  • a permanent employment contract
  • travel time = work time
  • highly competitive compensation packages including local allowances and additional insurances
  • regular, merit-based salary adjustments
  • significant employer contributions to an attractive pension scheme
  • excellent training and career development opportunities
  • strong support from Line Management, your team and more than 20'000 colleagues worldwide
  • the world's most renowned pharmaceutical companies and innovative biotech pioneers 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 careful source document review. Monitor data for missing or implausible entries
  • Perform the required monitoring tasks in an efficient manner, according to SOPs and established guidelines; prepare accurate and timely trip reports
  • Review progress of projects and initiate appropriate actions to achieve target objectives
  • Interact with internal work groups to evaluate needs, resources and timelines
  • Act as contact for clinical trial suppliers and other vendors as assigned
  • Complete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
  • Independently perform CRF reviews
  • Generate queries and resolve issues according to data review guidelines on Labcorp or sponsor data management systems


Your profile:
  • Degree in a relevant field such as life sciences, pharmacology, biology, chemistry, health care, health management, (veterinary) medicine, nursing, etc.; in lieu of the former, a completed vocational education or professional experience (e.g. as study nurse, study coordinator...)
  • Professional experience in a related function with a focus on independent site monitoring in Spain.
  • Familiarity with applicable Spanish and international regulatory requirements such as ICH / GCP
  • Computer literacy in Microsoft Office (Word, Excel, PowerPoint) and preferably in relevant software solutions for clinical trials, e.g. eTMF (e.g. Veeva Vault)
  • Effective time management and organizational skills and a keen attention to detail
  • Valid driver's license
  • Excellent communication skills in business fluent Spanish and English - both spoken and written - are a must

APPLY NOW

... so we can tell you about the cookies & brownie days, the sense of humor and team support that permeate everything we do, how our managers constantly review study/site allocation to ensure workload balance or why you will not grow a stale career with us

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 .

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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