Clinical Research Associate (CRA)

☞ Labcorp Drug Development

Ver: 220

Dia de atualização: 16-11-2025

Localização: Brussels Brussels Capital

Categoria: R & D IT - Software

Indústria: Hospitals Health Care

Posição: Entry level

Tipo de empregos: Full-time

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Conteúdo do emprego

Why settle for one thing when you can have everything.  Labcorp Drug Development gives you the best opportunity for career growth. Our Energizing Purpose, Exceptional People and Extraordinary Potential combined with collaborative and proactive teams offer a great place for you to continue honing your therapeutic skills and growing and excelling in new exciting research.

Our reach is global – extending to 60+ countries making us one of the largest CROs. So not matter where you are locating on the globe we have an opportunity for you.

We are seeking a CRAI/CRA II to be responsible for all aspects of study site monitoring and management including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.

Additional Responsibilities Include
  • Organize and make presentations at Investigator Meetings
  • Participate in the development of protocols and Case Report Forms as assigned
  • 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 as assigned
  • Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Labcorp or client data management systems as assigned by management
Requirements
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.
  • Minimum of at least1 yearof Onsite Clinical Monitoring experience along with at least 1 year total in clinical research experience is required. 
  • Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements
  • Thorough knowledge of monitoring procedures; Basic understanding of the drug accountability process
  • Valid Driver’s License
  • 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
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.

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 (https://www.labcorp.com/hipaa-privacy/web-privacy-policy) .
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Data limite: 31-12-2025

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