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Clinical Research Associate Mea

il y a 4 semaines

SintLambrechtsWoluwe, Belgique Labcorp Temps plein

Are you an Experienced Research Nurse, Clinical Trial Coordinator, or Clinical Study Coordinator?

Join Labcorp Drug Development Monitoring Excellence Academy (MEA) and train to be a CRA.

**If you bring the Oncology therapeutic expertise, we will train you to be a top-notch CRA.**

Job Responsibilities
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, the conduct of pre-study and initiation visits, with or without guidance; liaise with vendors; and other duties, as assigned
- Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
- Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
- Perform CRF review, query generation and resolution against established data review guidelines, with or without direct supervision, on Labcorp Drug Development or client data management systems, as assigned by management

**What Our MEA CRAs Have To Say**

**"My MEA training remains an amazing experience and I don't feel as though I will ever stop learning. And that is a GREAT feeling"**

**"MEA is fast-paced, focused, and best of all a family. At the heart of the program are its support and adaptability."**

**"Everyone in MEA takes pride in their work and makes the effort to be available every step of the way. I never felt alone through the Experience and I can honestly say I have never felt more prepared and supported in any job throughout my career."**

**Come join the Labcorp Drug Development team, where you can help impact the lives of millions**

Education / Qualifications

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
- Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements
- Basic understanding of the clinical trial process
- Valid driver's license

Experience
- ** A minimum of 2 years of experience in a related field (i.e. site management, in-house CRA, study coordinator, research nurse, etc.)**
- Valid driver's license
- ** Fluent in Dutch, French and English**

If you would like to learn more please contact:
**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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