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Senior Study Start-up Specialist, Sponsor-dedicated
3 weeks ago
As a Senior Start-Up Specialist you will ideally have a minimum of 4 years’ experience in clinical development or regulatory process and be fully proficient and independent in performing the following detailed role requirements. In addition, you will have been responsible for QC’ing work and the training of more junior members of staff.
Therefore, practical experience of related Ethics & HRA submissions within the applicable country portals will be essential.
Site contract negotiation is currently not a requirement.
The model is dedicated solely to meeting the contractual requirements of 1 specific Client/Sponsor, but has ambitions of future potential growth.
In a nutshell, this is a great opportunity to join a small but perfectly formed team of friendly start up specialists, who liaise closely with one Sponsor, in order to deliver all their country start-up and Clinical Trial maintenance requirements.
**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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