Job summary
Job post source
This job is directly from Pharmavise Corporation
Job overview
The Drug Safety Pharmaceutical Consultant role at Pharmavise Corporation involves providing expert pharmacovigilance consultation to pharmaceutical clients, ensuring drug safety and regulatory compliance to improve patient health.
Responsibilities and impact
The consultant will review adverse event reports, conduct signal detection, develop risk management plans, support regulatory submissions, and collaborate with cross-functional teams to maintain drug safety compliance.
Compensation and benefits
Competitive compensation packages are available; specific salary details and benefits are not provided.
Experience and skills
Candidates need an advanced degree in pharmacy or related fields, at least 5 years of drug safety experience, knowledge of global pharmacovigilance regulations, and experience with safety databases; certifications are preferred but not required.
Work environment and culture
Pharmavise values excellence through quality and promotes an inclusive, equal opportunity work environment with a focus on compliance and patient safety.
Company information
Pharmavise Consulting Corp. is a regulatory compliance consulting firm partnering with pharmaceutical, medical device, and biotechnology clients to address complex compliance issues.
Job location and travel
This is a remote position, allowing work from any location.
Application process
Applicants can contact info@pharmavise.com for accommodations or further information; specific application steps are not detailed.
Unique job features
The role offers the opportunity to work on complex compliance issues in drug safety with a focus on improving patient health and safety, collaborating with diverse clients and regulatory bodies.
Company overview
Pharmavise Corporation is a strategic partner for pharmaceutical, medical device, and biotechnology companies, offering expertise in quality, regulatory, and compliance services. Headquartered in Florida, the company supports clients from development to commercialization, ensuring adherence to industry standards. Founded by Ricardo Joseph, Pharmavise employs a team of professionals specializing in drug safety, GMP, and clinical subject matter expertise. The company's commitment to excellence is reflected in its diverse service offerings and its role as a trusted advisor in the life sciences and healthcare sectors.
How to land this job
Position your resume to highlight your expertise in drug safety and pharmacovigilance, emphasizing experience with adverse event reporting, signal detection, and risk management plans as outlined in the job description.
Showcase your knowledge of global pharmacovigilance regulations (FDA, EMA, ICH) and your familiarity with safety database systems like ARGUS or ARISg to align with Pharmavise's technical expectations.
Apply through multiple platforms including Pharmavise Corporation's official website and LinkedIn to maximize your visibility and chances of landing the role.
Connect with current employees in the drug safety or regulatory compliance division at Pharmavise on LinkedIn; use ice breakers such as commenting on recent company updates, asking about their experience with compliance challenges, or inquiring about the team culture.
Optimize your resume for ATS by integrating keywords from the job description like 'pharmacovigilance,' 'risk minimization strategies,' 'signal detection,' 'regulatory submissions,' and 'adverse event reports' to ensure it passes initial automated screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored resume adjustments, identify optimal application channels, and find relevant LinkedIn contacts, allowing you to focus your energy on preparing for interviews and networking effectively.
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