Senior Pharmacovigilance Manager

Reposted 5 Days Ago
Be an Early Applicant
Zug, CHE
In-Office
Senior level
Biotech • Pharmaceutical
The Role
Manage and support the EU Pharmacovigilance system, maintain the PSMF, ensure compliance with EU GVP, oversee affiliates and vendors, coordinate PV training, handle safety information and regulatory requests, assist inspections and audits, and act as back-up for Deputy EU QPPV and national PV contacts.
Summary Generated by Built In

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.

The Senior Pharmacovigilance Manager supports the EU QPPV Office in maintaining an effective Pharmacovigilance (PV) system in compliance with applicable European Union regulatory requirements, company procedures, and global PV standards. The role includes operational PV support, affiliate oversight, compliance activities, training coordination, PSMF maintenance, safety information management, and acting as a back-up for key PV functions including the Deputy EU QPPV and PV National Contact Persons (NCPs).

Key Responsibilities

EU QPPV Office Support

  • Support the EU QPPV Office in maintaining the EU Pharmacovigilance System in compliance with EU GVP requirements and internal procedures.

  • Contribute to the quarterly update and maintenance of the Pharmacovigilance System Master File (PSMF), including collection, verification, and reconciliation of required information from affiliates and functional stakeholders.

  • Support preparation and maintenance of PV governance documentation, metrics, and oversight activities.

  • Assist in inspections, audits, health authority requests, and PV readiness activities as required.

  • Support implementation and maintenance of PV processes, SOPs, work instructions, and quality documents.

Deputy EU QPPV / PV NCP Back-up Responsibilities

  • Act as designated back-up for the Deputy EU QPPV and Affiliate PV National Contact Persons, as applicable.

  • Ensure continuity of PV activities during planned or unplanned absences.

  • Support communication and coordination with affiliates, competent authorities, PV main vendors, and internal stakeholders when delegated.

PV Training

  • Coordinate and deliver PV training to affiliate employees, global and local vendors, distributors, and relevant service providers across the EU region.

  • Maintain training records and ensure compliance with training requirements.

Safety Information Management

  • Manage translation, reporting, reconciliation, and follow-up of safety information in accordance with regulatory timelines and company procedures.

  • Coordinate with affiliates and third-party providers to ensure timely submission and follow-up activities.

PV Compliance and Quality Activities

  • Support PV compliance monitoring activities, including metrics collection, trend analysis, and compliance reporting.

  • Assist affiliates with the management of PV deviations, CAPAs, and effectiveness checks.

  • Participate in root cause investigations and continuous improvement initiatives.

  • Support vendor oversight and compliance activities to PV agreements with service providers.

  • Contribute to preparation of internal PV audits and regulatory inspections

Cross-Functional Collaboration

  • Collaborate with Regulatory Affairs, Quality Assurance, Medical Affairs, and Cytokinetics affiliates to ensure PV compliance.

  • Support implementation of new regulatory requirements.

  • Participate in global and regional PV projects and initiatives as assigned.

Qualifications

Education

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Medicine, or related scientific discipline required.

Experience

  • Minimum 10 years of experience in Pharmacovigilance within the pharmaceutical or biotechnology industry.

  • Experience supporting EU Pharmacovigilance systems and GVP requirements.

  • Experience with PSMF maintenance, PV operations and compliance activities, and affiliate oversight

  • Experience in developing and delivering PV training to employees and external service providers

Knowledge & Skills

  • Strong knowledge of European Union Pharmacovigilance regulations.

  • Understanding of adverse event reporting requirements and PV quality systems.

  • Familiarity with CAPA management, deviations, inspections, and audit processes.

  • Excellent organizational skills and attention to detail.

  • Strong communication and stakeholder management skills.

  • Ability to work independently and collaboratively in a global matrix environment.

  • Proficiency in PV databases and Microsoft Office applications.

  • Fluency in English, and German required; additional European languages are an advantage.

Competencies

  • Compliance mindset and quality orientation

  • Strong analytical and problem-solving skills

  • Ability to manage multiple priorities and deadlines

  • Effective training and presentation skills

  • Team-oriented with strong interpersonal skills

Reporting Line

  • Reports to: Deputy EU QPPV

#LI-HYBRID

Pay Range:

Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you.

Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.  

Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves.

Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers

Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process.

Here are some ways to check for authenticity:

  • We do not conduct job interviews through non-standard text messaging applications

  • We will never request personal information such as banking details until after an official offer has been accepted and verified

  • We will never request that you purchase equipment or other items when interviewing or hiring

  • If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at [email protected]

Please visit our website at: www.cytokinetics.com

Cytokinetics is an Equal Opportunity Employer

Skills Required

  • Bachelor's degree in Life Sciences, Pharmacy, Nursing, Medicine, or related scientific discipline
  • Minimum 10 years of experience in Pharmacovigilance within the pharmaceutical or biotechnology industry
  • Experience supporting EU Pharmacovigilance systems and GVP requirements
  • Experience with PSMF maintenance, PV operations, compliance activities, and affiliate oversight
  • Experience developing and delivering PV training to employees and external service providers
  • Strong knowledge of European Union Pharmacovigilance regulations
  • Understanding of adverse event reporting requirements and PV quality systems
  • Familiarity with CAPA management, deviations, inspections, and audit processes
  • Proficiency in PV databases and Microsoft Office applications
  • Fluency in English and German (additional European languages advantageous)
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The Company
HQ: South San Francisco, CA
473 Employees
Year Founded: 1998

What We Do

Cytokinetics is a late-stage biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which muscle performance is compromised and/or declining. As a leader in muscle biology and the mechanics of muscle performance, we are developing small molecule drug candidates specifically engineered to impact muscle function and contractility. Proud to be a San Francisco Business Times Best Place to Work in 2021 and 2022, a Great Place to Work-Certified company in 2022 and a part of Fortune's Best Workplaces in the Bay Area in 2022 and Fortune's Best Workplaces in BioPharma in 2022.

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