Associate Director, Policy and Patient Advocacy
New Today
Associate Director, Policy and Patient AdvocacyRole focused on policy, patient advocacy, and external engagement within the rare disease space. The successful candidate will lead strategic initiatives to influence government and health system policy, engage with patient communities, and support the adoption of innovative therapies across the UK and Ireland.ResponsibilitiesDevelop and implement advocacy strategies to shape policy and support access to therapies in rare diseases.Build and maintain relationships with policymakers, patient organizations, trade associations, and other external stakeholders.Monitor and analyze emerging policy and political developments and provide strategic guidance to internal teams.Collaborate with cross-functional teams, including commercial, medical, and access teams, to ensure alignment on advocacy priorities.Support communications efforts to raise awareness of key initiatives and maintain consistent messaging across stakeholders.Required Skills & ExperienceSignificant experience (10+ years) in policy, government affairs, public affairs, or patient advocacy, ideally within healthcare, biotech, or pharmaceutical sectors.Proven ability to engage with senior policymakers, clinicians, and patient organizations.Strong experience in external affairs, including media engagement and trade association representation.Demonstrated skill managing complex, high-profile projects and cross-functional teams.Excellent strategic thinking, communication, and influencing skills.Track record of delivering measurable impact through advocacy and policy initiatives.QualificationsEducated to degree level or equivalent.Experience working in matrix organizations or global functions is preferred.Ability to work under pressure in a fast-paced, evolving environment.Strong business acumen and understanding of healthcare systems in the UK & Ireland.About Planet PharmaPlanet Pharma is an American parented employment business/agency that provides global staffing services with its headquarters in Chicago and an EMEA regional office located in Central London. We operate in 30+ countries with a current network of 2,500+ active contractors globally, offering permanent/direct hire recruitment services as well.We have extensive functional expertise including Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of race, sex, disability, religion/belief, sexual orientation or age.
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- Location:
- United Kingdom
- Job Type:
- FullTime