About this role
Role Overview
- Provides operational support for global pharmacovigilance activities for Grifols investigational and marketed products.
- Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines.
- Responsible for project implementation and execution of system, including responsibilities for providing safety ongoing business support and ongoing improvements.
- Key interface with the IT system administrators to verify and test system changes ensuring that the system is compliant and meets business needs.
- Support drug safety applications with business administration tasks.
- Key expert to deliver solutions that are cost effective, sustainable, and meet business requirements.
- Develop training documentation and/or work instructions to determine methods and procedures.
- Coordination and management of signal management.
Requirements
- Bachelor’s degree in a field within the Experimental or Health Sciences (e.g., Biology, Chemistry, Environmental Science, Health Sciences, or a related discipline).
- Biochemistry, Pharmacy, or Experimental Sciences – 3 years of experience in research-related roles
- Information Technology (Database Administration) – 6 years of experience in research or database administration roles
- At least 5 years of relevant experience in pharmacovigilance managing databases.
- Availability for international traveling when necessary is also required.
- Proven self-starter with strong work ethic and the ability to exercise good judgment.
- Ability to work independently with minimum supervision.
- Strong organizational, analytical, and problem-solving skills.
Benefits
- Health insurance
- 401(k) retirement plan
- Paid time off
- Flexible working arrangements