Start Up Associate
hace 1 mes
Collect and track all the necessary documents required and perform a quality review, formatting and compilation of the final documents for effective and compliant site activation and maintenance
Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines
Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner
With guidance from line manager and experienced colleagues, adapt Informed Consent Forms and other patient facing material to country specific requirements
May support / assist the contract negotiation process under supervision of an experienced colleague or line manager
Update study documents when there are changes in study personnel/study amendments
Ensure high quality documents are filed and systems are updated on an ongoing and timely basis making Labcorp ready for an audit at any time
Update status reports, applicable logs and tracking systems as applicable for the projects with input provided by senior staff
**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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Study Start Up Associate I
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Study Start Up Associate Ii
hace 24 horas
Ciudad de México ICON A tiempo completoAs a Study Start Up Associate II you will play a key role in improving the lives of patients by accelerating the development of our customers drugs and devices through innovative solutions. You will be dedicated resource to one of our clients, be embedded in their working environment, systems and processes. You will be engaged in a wide range of interesting...
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Study Start-up Manager, Mexico
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Associate, Employee Services, Us
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Assoc Proj Manager, Start-up
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Accounting Associate
hace 1 mes
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Development Associate
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Clinical Research Study Start-up Project Manager
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Operations Associate
hace 4 semanas
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Clinical Trial Associate Global
hace 1 mes
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Country Start Up Specialist
hace 3 días
Ciudad de México Medpace, Inc. A tiempo completoJob Summary: Join Medpace in Mexico! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with Regulatory...
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Scrum Master
hace 3 días
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Bilingual Customer Service Representative
hace 2 semanas
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Underwriting Associate
hace 1 mes
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Balenciaga Sales Associate Polanco
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Balenciaga Sales Associate Polanco
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Sales Associate
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Customer Support Associate
hace 2 semanas
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Manager -transaction Advisory Group
hace 1 mes
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Buyer
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