This is a remote position.
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at
Responsibilities:
Provide expert consultation and support in drug safety and pharmacovigilance to pharmaceutical companies and regulatory agencies.
Review and evaluate adverse event reports and safety data for investigational and marketed drugs, ensuring compliance with regulatory requirements and guidelines.
Conduct signal detection activities to identify potential safety concerns associated with drug products and collaborate with cross-functional teams to mitigate risks.
Develop and implement risk management plans (RMPs) and risk minimization strategies to optimize the benefit-risk profile of drugs.
Provide guidance on safety-related labeling updates, including drafting and review of product labels, package inserts, and risk communication materials.
Support regulatory submissions and interactions with health authorities related to drug safety, including responses to safety-related inquiries and requests for information.
Contribute to the development and implementation of pharmacovigilance processes and systems to ensure compliance with global regulatory requirements (e.g., FDA, EMA, ICH).
Stay abreast of emerging safety issues, pharmacovigilance trends, and regulatory developments in the pharmaceutical industry.
Qualifications:
Advanced degree in pharmacy, pharmacology, life sciences, or related field.
Minimum of 5 years of experience in drug safety and pharmacovigilance within the pharmaceutical industry, CRO, or regulatory agency.
In-depth knowledge of global pharmacovigilance regulations and guidelines (e.g., FDA, EMA, ICH), including experience with safety reporting requirements (e.g., ICSR, SUSAR).
Strong understanding of pharmacovigilance processes, risk management methodologies, and signal detection techniques.
Experience with safety database systems (e.g., ARGUS, ARISg) and adverse event case processing.
Excellent analytical and problem-solving skills, with the ability to interpret and communicate complex safety data and risk assessments.
Effective communication and collaboration skills, with the ability to interact with internal and external stakeholders, including health authorities.
Regulatory affairs certification (RAC) or drug safety certification (e.g., CSPV, RPhS) preferred but not required.
This is a challenging and rewarding opportunity for individuals passionate about drug safety and patient well-being. Competitive compensation packages are available.
Be part of our network of Subject Matter Experts.
EEO Employer:
Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com .
Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise , you become part of a team that values Excellence Through Quality.
Follow us in LinkedIn for more company updates and opportunities.
...with: Software, Engineering, Sales, Accounting, IT Primary Responsibility: We are seeking a highly motivated and experienced Product Owner to lead the development of digital solutions that align with our company's goals. Specific Duties and Responsibilities: ~...
...new product line that will transform the insurance broker experience through AI and machine learning. As an AI-Driven Full Stack Engineer, youll be part of a team charting new territory designing and implementing intelligent systems that automate manual processes and...
...Prairie View A&M University Police Records Technician II Job Title Police Records Technician II Agency Prairie View A&M University Department University Police Proposed Minimum Salary $13.66 hourly Job Location Prairie View, Texas...
...Dental Office Manager TimberRidge Dental is a company in Heber City, UT 84032. We are supportive, fun and our goal is to provide not only our patients with the best experience possible, but also to give our staff a positive and fulfilling place to work. We are searching...
...assignment. Onboarding will take place in Overland Park, KS. Union or Union management experience in the Electrical trade is... ...required, to direct hire workforce, subcontractor supervision or Construction Engineers. Ensures compliance by workforce or subcontractor to...