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EquipNet Auction: Lab & Analytical Instruments from Leading Biotech & Pharma Companies - May 24

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Seagen

Senior Manager Case Management

Development - Bothell, Washington

Description

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to improving the lives of cancer patients goes beyond science, and we believe that every employee has a role in contributing to this mission. By working together with a shared dedication and diverse perspectives, we are able to reach our full potential and make a real difference in the world. Seagen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Put your passion to work at Seagen and join us!

Summary

Seagen is currently offering a unique opportunity for a highly motivated individual to be part of growing Global Safety and Risk Management Team. The successful candidate will be responsible for ensuring all ICSR processing complies with local and international regulatory requirements, corporate and departmental procedures and applicable pharmacovigilance agreements. While the primary role of this position will focus on the operational management and oversight of case processing activities performed internally and externally by vendors (CROs) the ideal candidate will also provide scientific and strategic input to support efficient decision making for our Case Management Team.

Principal Responsibilities

  • Ensures all case management activities comply with regulatory requirements, corporate and departmental procedures and applicable Pharmacovigilance (PV) agreements.
  • Participates in the development and operational implementation of case management governing documents such as SOPs, work instructions, SMPs.
  • Leads oversight of case management vendor including training, evaluation of quality and issue management.
  • Works cross functionally with Safety Evaluations and Risk Management, Safety Systems team, Safety Compliance, QPPV, Local Safety Officers, Clinical Operations, Regulatory Affairs and Product Quality regarding safety data collection, analysis and reporting.
  • Provides AE/PC training for new PSP/MR/Medical Information as needed
  • Manages oversight of literature surveillance including training of vendors.
  • Manages oversight of reconciliation activities and regulatory authority database searches for ICSR reporting.
  • Supports/performs Case Processing, Submission, and reconciliation activities as required. Serves as Case Management representative for Business Partner and vendor Operational meetings.
  • Participates/assists in internal/business partner’s audit and regulatory inspections.
  • Provides subject matter expertise in the interpretation of regulations as it relates to ICSR processing and reporting.
  • Manages queries from Business Partners or vendors or internal team on case processing or submission activities.
  • Maintains metrics on current and projected Case Management workload.
  • Provides strong leadership to Case Management staff, including mentorship, training, performance management and creating opportunities for professional growth.
  • Provide ongoing leadership in staff career development and manage staff performance and oversee assignments including goal setting and providing Manager Performance Evaluation Assessments.
  • Work cross-functionally to establish and maintain priorities on projects impaction the function.

Qualifications:

  • N, B.S.N, RPh or PharmD
  • Minimum of 7 years in Drug Safety / Pharmacovigilance in biotech or pharmaceutical industry setting
  • Extensive experience in Clinical Trial and Post-marketing Case Management
  • Proficient in safety system (Argus). Working knowledge of MedDRA and WHO-Drug coding
  • Demonstrated experience working with cross functional areas with effective negotiation skills
  • Exceptional communication skills, both written and verbal
  • Excellent management and interpersonal skills
  • Vendor oversight and business partner collaboration experience

As the leading employer in our industry in the Pacific Northwest, Seagen is proud to offer a competitive total compensation package as well as a comprehensive benefits program designed to support the whole lives of our employees and their families. Benefits include medical, vision and dental coverage, group and supplemental life insurance, 401(k) with company match, tuition reimbursement, relocation assistance and much more. To learn more about Seagen, please visit www.seagen.com.

Seagen is an equal opportunity employer. All qualified applications will receive consideration for employment without regard to race, age, gender identity, sexual orientation, color, religion, sex, marital status, national origin, protected veteran status, disability status, or any other status protected by federal, state, or local law.

To prevent the spread of COVID-19, and as an integral part of its public health and safety measures, Seagen requires that all newly-hired employees be fully vaccinated against COVID-19 before commencing employment, subject to reasonable accommodation and other requirements of applicable federal, state, and local law.


Seagen

Seagen is an Equal Opportunity Employer

Submitted: 01/28/2022

EquipNet Auction: Lab and Analytical Instruments from Leading Biotech and Pharmaceutical Companies - May 24 @ 9 am EST




















 
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