Job Description

General Tasks

• Responsible for maintaining awareness of regulatory legislation, guidance and practice, ICH/GCP and relevant Sponsor requirements
• Take ownership in the preparation (collection, organization and compilation) of routine submissions filed to IRB/EC/Third body/Regulatory Authorities (e.g. INDs/CTAs) including but not limited to the preparation of study documentation such as review/summarize scientific/research documents, country application form and cover letter for sponsor review as applicable
• Complete submissions to and liaise with IRB/IEC/Third body/Regulatory Authority as applicable regarding submission/approval issues
• Liaise with internal and external vendors in the generation of Regulatory Authority submissions (as applicable)
• Perform a review of final submission documents as applicable
• Ensure appropriate systems are updated accurately and compliantly, ensuring others follow established processes
• Anticipate and prevent issues and service failures from developing in their study, escalating when appropriate, negotiating when required
• Mentor and coach other Site Readiness and Regulatory Operations team members
• Perform other duties as assigned by management depending upon country and situational requirements with proper supervision [if applicable]

In-Country specific tasks (Global)

• Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner
• 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 without supervision and liaise with stakeholders as applicable in site activation related items
• When delegated by line manager, oversee and ensure quality data and audit readiness
• Participate independently and take lead (as applicable) in client meetings to proactively liaise on issues related to site activation and maintenance
• Develop project specific plans for the Site Activation component of assigned studies
• Review and approve projections and timelines to study teams, ensuring that they accurately represent the country\xe2\x80\x99s performance and suggests mitigation actions in agreement with line manager
• Review and approve Country and Site Specific patient informed consents for compliance to local requirements and protocol with agreement by line manager
• Proactively resolve informed consent and contractual language issues plus other significant barriers to study execution with study sites
• Oversee start up activities (possibly across a range of studies) to ensure issues are identified, managed and, if necessary, escalated to the appropriate individual
• May take country lead role for specific projects/tasks with the applicable mentoring and supervision
• Proactively identifying, preventing and escalating to Submission Leads any risk to meeting deliverables and participate in strategy meetings to mitigate them
• Notify the Submissions Lead of hours identified as Out-of-Scope or over burn

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 .

Labcorp