Job Summary
We are seeking a highly skilled Deputy General Manager for our CDM/PV team with 5 to 7 years of experience in Pharma Research & Development. The ideal candidate will have a strong background in PV data management and PV case processing. This role is crucial for ensuring the safety and efficacy of our pharmaceutical products contributing significantly to public health.
Responsibilities
Lead the CDM/PV team to ensure accurate and timely data management.Oversee the collection processing and reporting of pharmacovigilance data.Provide strategic direction for PV case processing activities.Ensure compliance with regulatory requirements and company standards.Collaborate with cross-functional teams to support drug safety initiatives.Develop and implement data management plans and protocols.Monitor and analyze PV data to identify trends and potential safety issues.Coordinate with external partners and stakeholders for data exchange and reporting.Conduct regular audits and quality checks to maintain data integrity.Train and mentor team members on best practices in PV data management.Prepare and present reports to senior management on PV activities and outcomes.Contribute to the continuous improvement of PV processes and systems.Support the development of new pharmaceutical products by providing PV insights.
Qualifications
Possess a strong background in Pharma Research & Development.Have extensive experience in PV data management and PV case processing.Demonstrate excellent analytical and problem-solving skills.Show proficiency in regulatory requirements and industry standards.Exhibit strong leadership and team management abilities.Display effective communication and collaboration skills.Be detail-oriented with a focus on data accuracy and integrity.Have a proactive approach to identifying and addressing potential issues.Show commitment to continuous learning and professional development.Be capable of working in a fast-paced and dynamic environment.Demonstrate the ability to manage multiple projects simultaneously.Possess strong organizational and time management skills.Show a high level of professionalism and ethical standards.
Certifications Required
Certified Clinical Data Manager (CCDM) Certified Pharmacovigilance Professional (CPP)
