Manager, Pharmacovigilance Scientist

Apellis Pharmaceuticals; United States; On-site; USD 100,000 - 150,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Manager, Pharmacovigilance Scientist. The successful candidate will oversee pharmacovigilance activities, support clinical trials, and lead risk management efforts for the company's products. This strategic role requires strong analytical skills and experience in PV.

Benefits

401(k) plan with company match

Flexible time off

Paid family leave

Disability and life insurance

Qualifications

• Minimum 2-4 years’ experience in Pharmacovigilance.
• Must have pharmaceutical industry background.

Responsibilities

• Support product safety surveillance activities.
• Lead proactive PV and risk management planning.
• Participate in writing aggregate safety reports.

Skills

Excellent written and verbal communication

Ability to interact across multiple functions

Data analysis skills

Problem-solving ability

Organizational skills

Education

Degree in Pharmacy, Nursing, Epidemiology, or Biosciences

Job description

Join to apply for the Manager, Pharmacovigilance Scientist role at Apellis Pharmaceuticals

Join to apply for the Manager, Pharmacovigilance Scientist role at Apellis Pharmaceuticals

Position Summary

Reporting to the Head of PV Sciences, the Pharmacovigilance Scientist will be a key contributor focusing on strategic input, support in clinical trials, perform signal management activities and operational support for all Apellis products throughout the life cycle. In this new role, the successful candidate will be responsible for the oversight of PV activities, vendor and alliance management, and ongoing process improvement.

Position Summary

Reporting to the Head of PV Sciences, the Pharmacovigilance Scientist will be a key contributor focusing on strategic input, support in clinical trials, perform signal management activities and operational support for all Apellis products throughout the life cycle. In this new role, the successful candidate will be responsible for the oversight of PV activities, vendor and alliance management, and ongoing process improvement.

Key Responsibilities Include

• Support product safety surveillance activities for assigned product(s) during all phases of the product life cycle.
• Provide PV support for Apellis’ developmental products in close collaboration with PV Physician and Clinical personnel.
• Lead/conducts proactive PV and risk management planning of multiple products, including preparation of the safety aspects of Global Risk Management Plans (RMPs) and Risk Evaluation and Mitigation Strategies (REMS) in partnership with the PV Physician and other stakeholders.
• Conduct signal detection, including adverse event data, literature, and other sources in collaboration with PV Physician and according to Apellis Signal Management and Safety Governance process.
• Perform data analysis to evaluate safety signals and write up analysis results.
• Partner with cross-functional colleagues of the Signal Management Team and contribute to safety-related deliverables associated with new drug applications, benefit-risk assessments and activities related to risk minimization including RMPs and REMS.
• Assist with developing and maintaining processes that will ensure excellence in global case reporting and assessment, demonstrating accuracy, consistency, and compliance with applicable global pharmacovigilance regulations.
• Participate in aggregate reporting, clinical trial activities, signal management, literature review, and ad hoc regulatory responses for assigned product group.
• Review and provide PV input for development of protocols, Investigator Brochures, Statistical Analysis Plans, Clinical Study Reports, and other relevant project/study documents.
• Support pharmacovigilance activities including ongoing signal management and regulatory activities.
• Facilitate cross-functional safety review meetings, including coordinating aspects of signal evaluation/safety review activities.
• Participate in writing of aggregate safety reports (e.g., DSURs, PSURs, PADERs), as required.
• Assist in the successful implementation, execution, and maintenance of safety processes and systems that conform to the company’s business strategy, industry standards and compliance with global PV regulations.
• Represent Drug Safety and PV on clinical teams and initiatives both within and across functional areas.
• Facilitate cross-functional safety review meetings, including coordinating aspects of signal evaluation/safety review activities.
• Participate in evaluation of potential safety issues in conjunction with PV Physician, Medical Monitors, and other functional areas as appropriate.
• Participate in writing of PV input for regulatory submissions and regulatory responses, collaborating with cross-functional areas as appropriate.
• Assist with writing and maintenance of Pharmacovigilance Agreements.
• Assure oversight for the review of aggregate safety data to ensure accuracy, integrity and completeness.
  
  

Education, Registration & Certification

• Degree in Pharmacy, Nursing, Epidemiology, Biosciences (e.g., Biology) or equivalent healthcare degree with pharmaceutical industry background.
  
  

Experience

• Minimum 2-4 years’ experience in PV.
  
  

Skills, Knowledge & Abilities

• Excellent written and verbal communication skills with the ability to interact across multiple functions.
• Experience in the preparation and authoring of individual and aggregate safety reports.
• Knowledge of MedDRA terminology and its application.
• Experience reviewing cumulative safety data with ability to interpret, synthesize and communicate complex safety information.
• Demonstrated ability to develop, execute and follow-through complex projects to completion.
• Skilled at working effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view.
• Independently motivated, detail oriented and strong problem-solving ability.
• Excellent organizational skills and demonstrated ability to multi-task in a fast-paced environment with changing priorities.
  
  

Physical Demands And Work Environment

• This is largely a sedentary role; however, some filing is required. This would require the ability to lift files, open filing cabinets. This job operates in a professional office environment and routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.
  
  

Travel Requirements

• Up to 20% travel expected.
  
  

Benefits And Perks

Apellis offers a comprehensive benefits package, including a 401(k) plan with company match, inclusive family building benefits, flexible time off, summer and winter shutdowns, paid family leave, disability and life insurance, and more! Visit https://apellis.com/careers/benefits/ to learn more.

Company Background

Apellis Pharmaceuticals, Inc. is a global biopharmaceutical company that combines courageous science and compassion to develop life-changing therapies for some of the most challenging diseases patients face. We ushered in the first new class of complement medicine in 15 years and now have two approved medicines targeting C3. These include the first and only therapy for geographic atrophy, a leading cause of blindness around the world. With nearly a dozen clinical and pre-clinical programs underway, we believe we have only begun to unlock the potential of targeting C3 across many serious diseases.

For more information, please visit http://apellis.com or follow us on Twitter and LinkedIn

EEO Statement

Apellis is an equal opportunity employer and complies with all applicable federal, state and local fair employment practices laws. Apellis strictly prohibits and does not tolerate discrimination against employees, applicants or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including gender nonconformity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past, current or prospective service in the uniformed services, genetic information, marital status, AIDS/HIV status, smoker/nonsmoker, and occupational pneumoconiosis or any other characteristic protected under applicable federal, state or local law.

For San Francisco postings: Pursuant to the San Francisco Fair Chance Ordinance, we will consider for employment qualified applicants with arrest and conviction records.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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