Job Description

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. The Medical Affairs Group at Azurity is hiring a highly motivated Drug Safety Associate to join the team. This individual will report to the Director of Drug Safety and will support Pharmacovigilance activities across the organization. Assist in maintaining compliance with Pharmacovigilance (PV) activities in accordance with company policies, SOPs, and FDA regulations Assist in safety agreement editing, renewal tracking, and formatting. Assist with the management and oversight of safety-related information Assist with individual case review and management including company-sponsored clinical trials Assist with the management of the core drug safety email system Assist in managing and tracking reconciliations between partners Manage daily workflows and communications cross-functionally to ensure timely responses to partners Assist in the review, oversight, and organization of weekly and monthly safety reports Assist in organizing safety project management internal tools Assist in reviewing, organizing, and authoring standard operating procedures Assist in maintaining electronic files to ensure the filing of applicable documents to ensure audit readiness Assist in reviewing Expedited and Non-expedited safety reports and source documents including review for completeness and accuracy Contribute adverse event information for safety reports including Periodic Adverse Drug Experience Reports (PADERs), Post-Marketing Periodic Safety Update Reports (PSURs) as well as safety data for clinical reports Assist in maintaining pertinent workflows to increase the quality and submission of reports Assist in the preparation and editing safety related training materials Collaborate with other departments to ensure the timely processing of reports Maintains the integrity of confidential information throughout the work process Qualifications and Education Requirements Bachelor’s or master’s degree in life science or healthcare-related field OR equivalent combination of education and experience (i.e., an information science degree with at least 3 years of relevant working knowledge of supporting drug and patient safety) At least 3 years of experience reviewing individual case reports, aggregate reports and literature for adverse event reporting Strong analytic ability to analyze and summarize the main points of case reports, studies, and/or specific topics Possess experience with literature and safety databases Problem-solving skills, especially with respect to enforcing safety rules and global procedures as described in SOPs, Operational Manuals, and Guidance Documents Excellent written/oral communication skills are essential including fluency in English Proactive behavior and ability to keep timelines in a fast-paced environment Ability to develop cooperative working relationships with all levels of staff Conversant in medical terminology; familiarity with MedDRA coding Maintains comprehensive proficiencies with Adobe Acrobat and Microsoft Office (e.g., Word, Excel, and PowerPoint) and associated modules Possess a working knowledge and an understanding of FDA Regulations Ability to work independently and as part of a team in a fast-paced environment. Physical & Mental Requirements: Must be able to sit for long periods of time While performing the duties of this job, the employee is frequently required to stand; walk; sit; talk and/or hear May occasionally climb stairs and/or ride elevators The employee must occasionally lift and/or move up to 25 pounds Employee must be able to manipulate keyboard, operate a telephone and hand-held devices Other miscellaneous job duties as required Benefits We Offer: Unlock Your Earning Potential: Join our team and be rewarded with a competitive compensation package, including an annual bonus based on company performance, that recognizes your exceptional talent. Comprehensive Health Coverage: We value your well-being and offer excellent medical, dental, vision, and prescription coverage to ensure you and your family are always taken care of. Flexibility for Your Lifestyle: Achieve work-life balance with our hybrid work model, allowing you to work two days from home and three days in the office. Invest in Your Future: Our Retirement Savings Plan (401K) is designed to help you secure a comfortable retirement by matching dollar for dollar up to 5%. Time Off That Counts: Take advantage of our generous time off policy, which offers up to 15 vacation days annually + rollover (up to 40 hours) as well as five sick/wellness days. Meaningful Time with Your Loved Ones: We close between Christmas and New Year’s to give you an extra week off to spend quality time with your family and recharge. Enjoy the Holidays: Over the course of the year, Azurity recognizes 13 holidays. Invest in Your Education: We support your professional growth with tuition reimbursement for undergraduate and graduate level courses or certifications. Recognize and Be Recognized: Our Azurity High Five peer recognition platform allows you to celebrate your colleagues' accomplishments and receive recognition for your own outstanding work. Azurity Pharmaceuticals is an Equal Opportunity Employer and welcomes applications from diverse candidates. #J-18808-Ljbffr Azurity Pharmaceuticals

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