Director, Medical Affairs — Digital Therapeutics Strategy

Click Therapeutics, Inc.

New York (NY)

Hybrid

USD 175.000 - 220.000

Vollzeit

Vor 10 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Health benefits

Zusammenfassung

Click Therapeutics, Inc. seeks a Director of Medical Affairs to lead scientific strategy, evidence generation, and medical communications for a portfolio of digital therapeutics. You will manage evidence plans, engage with clinicians and payers, and oversee medical reviewers and CRO vendors in a regulated environment.

This senior role reports to the VP of Medical Affairs and operates in a rapid-growth, pre-IPO setting with hybrid work from Tribeca, NYC, or remote options.

Qualifikationen

  • Advanced degree required (MD, DO, PhD or PharmD).
  • 10+ years in industry, academia, clinical research, or related clinical practice, with at least 5 years in pharma.
  • Demonstrated experience building medical value stories and scientific narratives.
  • Experience planning and executing evidence and publication strategy, including CRO/agency management.
  • Prior field-based experience (MSL) with peer-to-peer scientific relationships.
  • Strong analytical judgment to interpret trial data and identify gaps.

Aufgaben

  • Define the medical strategy for each asset and guide evidence generation and engagement.
  • Own the evidence plan addressing clinicians and payers' needs and drive its execution.
  • Develop Core Medical Narrative and payer-facing medical content and publications.
  • Lead external engagement with experts, payers, and major congresses.

Kenntnisse

Analytical thinking
Scientific communication
Research ethics

Ausbildung

Advanced degree (MD/DO/PhD/PharmD)

Jobbeschreibung

Click Therapeutics, Inc. seeks a Director of Medical Affairs to lead scientific strategy, evidence generation, and medical communications for a portfolio of digital therapeutics. You will manage evidence plans, engage with clinicians and payers, and oversee medical reviewers and CRO vendors in a regulated environment.

This senior role reports to the VP of Medical Affairs and operates in a rapid-growth, pre-IPO setting with hybrid work from Tribeca, NYC, or remote options.

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