• Analyzing and Programming of Clinical Trials data
• Test data equivalent to Clinical Trial data will be provided and the candidates are to analyze & report their findings.
• The project scope is to understand the drug development process; it’s evolution into modern day methods of drug design. This gives the insight on the various components like the clinical trial protocol, informed consent form, case report form, and all regulatory submissions for IND application and NDA applications.
• It also helps candidates in getting a good knowledge on the clinical data understanding, organizing, analyzing, and finalizing reports for efficacy and safety for the new development product.
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 (https://www.labcorp.com/hipaa-privacy/web-privacy-policy) .
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