Pharmacovigilance Quality Analyst, 12-Month Contract
About The Position
This is a 12-month contract role supporting the Alexion Patient Services Team for all US approved products. The Pharmacovigilance Quality Specialist will be responsible for collecting, analyzing, and interpreting data related to adverse events. This role will also provide critical assistance within Patient Services and across Alexion's Commercial organization. The company fosters a collaborative culture that encourages innovation and a diverse environment where contributions are valued, allowing employees to be at the forefront of rare disease research and make a meaningful difference in patients' lives.
Requirements
- 1+ years of experience in the healthcare/rare disease industry OR recognized equivalent of education and experience (e.g., case management, social service support, insurance reimbursement, patient advocacy, etc.)
- Strong organizational skills and ability to adapt to change and react constructively in a high-energy and fast paced environment
- Passion for patient-centric strategies
- Strong verbal and written communication skills, attention to detail and time management
- Strong interpersonal skills and professionalism
- Independent problem solver, good decision maker, and robust analytical skills
- Ability to coordinate multiple assignments simultaneously and work independently
- Ability to use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.
Nice To Haves
- 1+ years of pharmaceutical/biotech experience
- 1+ years of Patient Services experience
- Proficient Windows based experience includes fundamentals of data entry/typing
- Experience working on a Salesforce platform
- Working knowledge of Outlook, Word, and Excel
- Experience using critical thinking to align corporate strategies and current challenges to develop recommendations
Responsibilities
- Supporting Patient Services with pharmacovigilance activities
- Case Processing: Collecting and reporting adverse events (AEs) and other safety information reported from various sources in accordance with applicable work instructions and global/local regulatory requirements
- Work with multidisciplinary teams to ensure accurate and complete safety data and adherence to regulations
- Participate in pharmacovigilance training and support the quality team to ensure compliance with requirements
- Completing quality review of work as part of finalizing adverse event submissions
- Responding to additional information requests from Global Patient Services regarding reported adverse events
- Identify potential trends through data analysis
- Document management
- Support Workforce Manager with Patient Services scheduling
- Support Data Intake and Quality initiatives
- Maintain confidentiality regarding patient specific information
Benefits
- Contract Benefits Program
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
