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Clin Res Assoc I
hace 2 semanas
**Job Summary**:
Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.
**Experience**:
Minimum Required:
- Six (6) months experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)
- Basic understanding of Regulatory Guidelines - Ability to work within a project team
- Good planning, organization and problem solving skills
- Good computer skills with good working knowledge of a range of computer packages
- Works efficiently and effectively in a matrix environment
- Valid Driver's License Preferred:
- One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
- 6 months on site monitoring experience
**Education/Qualifications/Certifications and Licenses**
Minimum Required:
- 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.
- Basic knowledge of Regulatory Guidelines
- Basic understanding of the clinical trial process
- Fluent in local office language and in English, both written and verbal
**_ 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._ _
**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.
For more information about how we collect and store your personal data, please see our Privacy Statement.
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