- Serve as the primary point of contact for project-related communications with
both external and internal stakeholders.
- Establish and maintain strong client relationships, ensuring consistent delivery of
high-quality work and addressing any concerns promptly.
- Develop project scope, timelines, and objectives based on the signed agreement
between the client and Navatio Pharma.
- Plan, track, and manage project activities, ensuring deadlines are met and
milestones are achieved on time.
- Oversee and report project progress, providing regular updates to clients and
internal stakeholders (e.g., Monthly reports, used for invoicing and performance
tracking).
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Monitor and manage project budgets, resource allocation, and timelines to ensure
efficient project execution.
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Ensure compliance with relevant regulatory requirements and adherence to internal
SOPs and Quality standards.
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Facilitate project meetings, ensure clear communication of goals, and resolve any
issues that may arise during the project lifecycle.
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Coordinate with cross-functional teams (e.g., safety operations, medical affairs,
regulatory affairs) to ensure successful project execution.
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Support the preparation and submission of safety reports, such as PADERs, PSURs,
DSURs, and other regulatory documents.
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Train and mentor staff in pharmacovigilance processes, regulatory requirements, and
best practices.
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Prepare for and support pharmacovigilance audits and regulatory inspections.
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Implement corrective actions as necessary following audits and inspections.
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Stay up to date with the latest trends and regulatory changes in pharmacovigilance.
Join us and be a part of a dynamic team ensuring patient safety worldwide!
Apply now or refer a suitable candidate!
Email your resume to:
: hr@navatiopharma.com