Senior Pharmacovigilance Associate
Salário Estimado
R$ 14.400,00 - R$ 21.600,00
Descrição da Vaga
This role offers the opportunity to contribute directly to patient safety by ensuring the effective monitoring, evaluation, and reporting of drug safety data in a regulated pharmaceutical environment. You will play a key role in managing post-marketing pharmacovigilance activities, supporting the detection of safety signals, and ensuring compliance with global regulatory requirements. Working within a collaborative, cross-functional team, you will interact with medical, clinical, and regulatory stakeholders to assess adverse events and contribute to risk management strategies. The position requires strong analytical capabilities and attention to detail, as well as the ability to manage complex safety data in a fast-paced environment. You will also support continuous improvement of pharmacovigilance processes and help maintain high standards of compliance and data integrity. This is an excellent opportunity for an experienced pharmacovigilance professional looking to make a meaningful impact on public health and drug safety.
Accountabilities
- Lead the collection, evaluation, and processing of adverse event reports, ensuring timely and compliant reporting according to regulatory guidelines.
- Analyze safety data to identify trends, assess potential safety signals, and support further investigation when required.
- Prepare and submit periodic safety update reports (PSURs) and other regulatory safety documentation in accordance with global requirements.
- Collaborate with medical and clinical teams to assess the clinical relevance of adverse events and support risk management activities.
- Ensure accuracy, integrity, and compliance of pharmacovigilance databases and safety documentation.
- Participate in regulatory audits and inspections, ensuring full preparedness and adherence to applicable standards.
- Provide guidance, training, and mentorship to junior team members on pharmacovigilance processes and best practices.
- Monitor and apply evolving regulatory guidelines to ensure continuous improvement of pharmacovigilance activities.
- Contribute to the optimization of safety workflows and support process enhancements across pharmacovigilance operations.
- Maintain confidentiality and ensure proper handling of sensitive patient safety information at all times.
- Bachelor’s degree in life sciences, pharmacy, nursing, or a related field; advanced degree preferred.
- Strong experience in pharmacovigilance, drug safety, or post-marketing safety surveillance within the pharmaceutical industry.
- Solid understanding of global pharmacovigilance regulations and industry standards.
- Proven experience in adverse event reporting, safety data evaluation, and signal detection processes.
- Strong analytical and critical thinking skills with the ability to interpret complex safety data.
- Experience working with pharmacovigilance databases and safety data management systems.
- Proficiency in Microsoft Office Suite and related reporting tools.
- Excellent communication and interpersonal skills, with the ability to collaborate across multidisciplinary teams.
- Ability to manage multiple priorities effectively in a fast-paced and regulated environment.
- Strong attention to detail and commitment to accuracy and compliance.
- High level of integrity and ability to handle confidential and sensitive information responsibly.
- Ability to work independently while contributing effectively to team objectives.
- Competitive compensation package aligned with industry standards.
- Comprehensive health insurance options for employees and their families.
- Various annual leave entitlements supporting work-life balance.
- Retirement savings and pension planning options.
- Life assurance coverage.
- Global employee assistance program providing 24/7 support services.
- Flexible country-specific benefits including childcare support, gym memberships, and transportation subsidies.
- Opportunities for professional development and career growth in a global organization.
- Inclusive and supportive work environment focused on well-being and belonging.
We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.
We appreciate your interest and wish you the best!
Why Apply Through Jobgether?
Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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