Drug Safety Public Health Specialist - II

OVERVIEW


We are currently seeking a skilled Drug Safety Public Health Specialist to join a well-known client’s Pharmacovigilance team in an on-site role based in Foster City, CA. This position supports global drug safety operations by ensuring compliance with pharmacovigilance regulations and managing adverse event (AE) data. The Specialist will play a critical role in patient safety and regulatory compliance, making a meaningful impact on public health.



RESPONSIBILITIES


•    Perform operational pharmacovigilance activities including the collection, review, evaluation, processing, and submission of adverse event (AE) information


•    Ensure compliance with internal procedures and global regulatory requirements


•    Independently perform routine and non-routine case management activities


•    Provide guidance and support to junior team members as needed


•    Actively participate in internal and cross-functional teams as a functional representative


•    Lead functional workstreams and projects of high complexity


•    Identify issues within pharmacovigilance processes and proactively propose solutions


•    Assist management as needed in issue resolution


•    Serve as a point of contact for internal and external stakeholders


•    Develop, review, and/or support quality review of safety data


•    Provide input into team training initiatives and lead trainings or onboarding activities as required


•    Represent the functional group in cross-functional project meetings



EXPERIENCE


•    Experience performing pharmacovigilance and drug safety case management activities required


•    Experience working with adverse event data and safety reporting processes


•    Experience leading projects, training initiatives, or functional workstreams preferred


•    Experience collaborating in cross-functional teams within a regulated environment



EDUCATION


•    Minimum of a Bachelor’s Degree in Public Health, Life Sciences, Nursing, Pharmacy, or a related discipline required



To be a best-fit, your strengths must include:


•    Strong understanding of pharmacovigilance principles and regulatory requirements


•    Excellent attention to detail and data quality


•    Strong analytical and problem-solving skills


•    Effective written and verbal communication skills


•    Ability to work independently while supporting team objectives


•    Proven ability to lead training activities and complex projects


•    Ability to proactively identify issues and recommend process improvements


•    Strong collaboration and stakeholder engagement skills



 

Full-time employees are also eligible for benefits options such as health coverage, life insurance, disability insurance, and 401k benefits.

At Advanced Group, our commitment to diversity and inclusion in every part of our organization is crucial to fulfilling our mission and demonstrating our REAL values. Advanced Group is committed to providing employment opportunities without regard to sex, race, color, age, national origin, religion, gender identity or expression, sexual orientation or sexual preference, pregnancy or maternity, genetic information, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.

Advanced Group complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities. If a reasonable accommodation is needed to participate in the job application or interview process, please contact accommodationrequest@advancedgroup.com.


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