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BeOne

Global oncology therapeutics discovery, development, manufacturing

Director – PV Alliance Management

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeRemote in USA$185.1k - $245.1k /yr

About the Job

Requirements

  • A bachelor's degree in life sciences, pharmacy, nursing, or equivalent is required; an advanced degree such as an MS, Ph.D., PharmD, or JD is preferred.
  • At least 8 years of experience working with pharmacovigilance contracts and/or alliance management is required.
  • Deep understanding of complex partnerships, including co-licensing, co-development, and clinical services, is required.
  • Expert negotiation skills and demonstrated ability to identify areas of mutual interest to achieve agreement are required.
  • Demonstrated experience managing resources responsible for PV contracts and/or alliance management is required.
  • Expert command of global pharmacovigilance agreement regulations and guidelines, including EU Good Pharmacovigilance Practices, Good Clinical Practice, and CDx, is required.
  • A proven track record of supporting compliance within the pharmacovigilance space is required.
  • Strong interpersonal and presentation skills, including the ability to liaise with senior leaders, are required.
  • Excellent oral and written communication skills are required.
  • Ability to deal with ambiguity and make decisions in a high-growth, rapidly evolving environment is required.
  • Strong analytical and strategic thinking skills with attention to detail are required.
  • Strong experience with Microsoft Office Suite, project management and collaboration tools such as Smartsheet, and familiarity with lifecycle contract management tools are required.
  • Ability to learn and apply new application skills, particularly using AI and automation, is required.

Responsibilities

  • Lead the global PV Alliance Management team and ensure the global strategic approach and day-to-day operating requirements for pharmacovigilance partners are managed effectively and objectives are achieved.
  • Contribute to the tools, processes, and strategies used by Global Patient Safety to coordinate business partners and proactively manage compliance risks.
  • Provide expertise, leadership, and direction in business partnerships relating to development, commercialization, medicinal products, and devices.
  • Track business development and commercial activities across the company to ensure pharmacovigilance and contractual obligations are met.
  • Lead pharmacovigilance due diligence and business development activities as requested, and oversee subsequent implementation actions.
  • Advise the business on pharmacovigilance contract and agreement requirements and participate in planning activities supporting business development.
  • Work with Global Patient Safety leadership to establish partner strategy across disciplines, align across pillars, and support implementation of pharmacovigilance requirements.
  • Deliver timely inputs supporting Global Patient Safety department business plans and priorities.
  • Oversee business partner relationships to promote collaboration and compliance with pharmacovigilance, CDx, and other requirements.
  • Maintain infrastructure for communicating responsibilities and obligations from PVAs and other contracts to relevant staff, including PVA management tools and systems.
  • Serve as a key contact on business partnerships for internal stakeholders and external business partners.
  • Provide oversight of pharmacovigilance contracts and agreements on behalf of the EU QPPV.
  • Oversee contractual obligations and associated deliverables throughout business partnership lifecycles.
  • Ensure accountable functions are aware of and comply with PVAs, PV clauses, and obligations.
  • Identify risks or disagreements with business partners and address them promptly, engaging Global Patient Safety leadership as needed.
  • Lead the identification and resolution of issues with pharmacovigilance alliances and partnerships.
  • Contribute to maintaining legal procedures used to execute pharmacovigilance contracts.
  • Manage and track PV contracts and agreements, including PVAs, PV clauses, and associated templates.
  • Plan and conduct best-practice and knowledge-sharing forums with internal stakeholders and external advisory groups.
  • Lead preparation, negotiation, and conclusion of SDEAs and PVAs for development, licensing, clinical service agreements, clinical supply, and commercial partnerships.
  • Work with potential partners and the internal Legal team on agreements and contracts.
  • Understand and communicate contractual obligations internally and externally to ensure compliance.
  • Collaborate with the PV Compliance group to address and resolve PVA-related compliance issues.
  • Support local and regional affiliates and business partners in reviewing and executing pharmacovigilance contracts.
  • Ensure the integrity of PV agreement content incorporated into the Pharmacovigilance System Master File.
  • Ensure compliance with company guidelines, legal and regulatory requirements, and industry practice.
  • Contribute to internal audits of pharmacovigilance contractual partners and support management of audit outcomes.
  • Serve as a subject matter expert for audits and inspections of the Global Patient Safety pharmacovigilance system.
  • Supervise personnel involved in negotiating and executing PV alliance contracts and agreements.

About the Company

BeOne

Global oncology therapeutics discovery, development, manufacturing

BeOne Medicines discovers, develops, and commercializes oncology therapies worldwide, focusing on hematologic cancers and solid tumors. Its products work by leveraging internal R&D and clinical development to bring therapies to market quickly, with Brukinsa serving as a leading backbone in the US and European markets. It differentiates itself through a large-scale global clinical network and cost-efficient development and manufacturing that support high margins and a focus on large-market cancer indications. Its goal is to expand access to high-impact, affordable cancer treatments across more than 45 countries while growing its pipeline into immunology and solid tumors.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Dongcheng District, China
Founded
2010

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