Job Description
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.
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.
...seamless access to care. Leveraging flexible hours and a remote working environment, I aim to enhance the mental healthcare experience for... ...in-person or remotely via telehealth while working from home. We accept the following licenses on a state by state basis:...
Key Skills:Drupal, PHP, Angular, CSSAt least 10+ years of Information Technology experience.2-3 years' experience in Drupal 8/9 or... ...effectively in the command line interface, Git, GitLab.Ability to develop, review, and test custom Drupal modules and themes.Good...
...Summary:**You will be responsible to install various types of telecommunications/security cabling and devices, camera, electronics and components to include but not limited to fiber optic cable and connectors, access control cabling and hardware including the installation...
Established in 1855, Southwestern Advantage is the oldest entrepreneurial program for college students in the world. Utilizing the single-level direct sales business model, college and university students run their own business selling educational resources to families...
...Licensed Psychiatric NP at Headway summary: As a Licensed Psychiatric Nurse Practitioner, you have the opportunity to build and manage your own private practice while receiving support from Headway. This role emphasizes flexible scheduling, hassle-free insurance credentialing...