In this role, you will liaise with a variety of internal groups and stakeholders, communicate with the safety organizations of the respective partners, and ensure compliance with regulatory requirements and company policies while facilitating effective collaboration across internal teams and external partners.Job Description
Support end to end PVA and SDEA activities with business partners. These activities include without limitation:
- Assist in the preparation, review, and maintenance of PVAs and SDEAs, with enhanced focus on PVAs for clinical studies.
- Support the initiation, negotiation, and revision of PVAs with business partners.
- Contribute to the development and maintenance of global PVA/SDEA templates.
- Coordinate communication with internal groups (e.g., Business Development, Commercial, Legal, Quality) and external partners to support PVA preparation and execution.
- Liaise with relevant stakeholders to facilitate PVA implementation, including database configurations and procedure updates.
- Provide training and guidance to internal/external stakeholders to ensure understanding of PVA terms.
- Conduct reconciliations and support monitoring activities in line with PVA obligations.
- Collaborate with relevant teams to address and resolve PVA compliance issues.
- Conduct periodic reviews of PVAs to ensure adherence to regulatory requirements, GE HealthCare business practices and the terms/status of the commercial agreement(s).
- Ensure accurate documentation and proper archiving of PVAs/SDEAs.
- Stay informed of regulatory and legislative changes impacting PVAs/SDEAs.
- Assist in updating PVA processes as directed by senior management.
- Coordinate and support the management of multiple PVA/SDEA-related projects simultaneously, ensuring timelines and deliverables are met.
- Escalate PVA issues to senior management as appropriate.
- Perform other PV related duties as assigned.
Required Experience, Skills, and Qualifications
- Bachelor’s degree in life sciences, pharmacy, regulatory affairs, or related field.
- Experience in pharmacovigilance and/ or contract coordination.
- Knowledge of pharmacovigilance processes and various types of business.
- Comprehensive knowledge of the drug development process.
- Strong organizational and multitasking skills with attention to detail.
- Excellent communication and interpersonal skills.
- Demonstrated strong teamwork/collaboration skills.
- Proficiency in MS Office Suite and familiarity with pharmacovigilance databases.
- Travel as needed.
GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.
Relocation Assistance Provided: No
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