Harrow, Inc.

Harrow, Inc.

Associate Director of Clinical Affairs

United States · Director

Sponsorship not specifiedDetected 8 days ago
ExpressStatisticsClinical TrialsClinical ResearchResearchPublic SpeakingMicrosoft Office

About the role

  • The Associate Director of Clinical Affairs is a key contributor to the creation and execution of the Clinical Affairs strategy and tactics.
  • This position will be involved in all aspects of Clinical Affairs such as designing and supporting clinical studies, protocol development, clinical site evaluations, as well as clinical study execution

Responsibilities

  • Support Clinical Operations and Clinical Development to facilitate enrollment of company-sponsored clinical trials.

Requirements

  • A minimum of 4 years of pharmaceutical industry experience, preferably in Ophthalmology, in a Clinical Affairs or Clinical Operations capacity required.
  • Successful record in designing and executing clinical trials required.
  • Strong analytical skills, ability to interpret scientific/clinical literature.
  • Fluency in reading, writing, understanding, and communicating in English is required.

Nice to have

  • An expanding Retina Portfolio including IHEEZO ®, TRIESENCE ®, BYOOVIZ TM, and OPUVIZ TM
  • A broad Dry Eye Disease product line, led by VEVYE ® and bolstered by well-known adjacent ocular surface disease products such as FLAREX ® and FRESHKOTE ®
  • A peri-operative Surgical product line, led by TRIESENCE ®, and BYQLOVI TM
  • A Rare and Specialty product line, which includes various high-need and utility products such as ILEVRO ®, NATACYN ®, and VERKAZIA ®
  • A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01
  • Execute Clinical Affairs strategies, including engagement with opinion leaders, principal investigators, and intracompany collaborators.
  • Oversee clinical research organizations (CROs) as they engage on Harrow sponsored clinical studies from start-up through close-out.
  • Provide timely responses to regulatory-oriented queries in relation to Harrow-sponsored clinical studies planned, in progress, or executed.

Benefits

  • Work collaboratively with cross-functional colleagues (e.g. marketing, sales, patient advocacy, medical affairs, regulatory, legal and market access) to develop and execute clinical plans.
  • Proven ability and experience to develop and foster peer-to-peer, credible relationships with Medical Experts/decision makers.

Company info

  • Before reading the job post, we encourage you to watch this video about our company.
  • It gives you an inside look at how we started, the team and culture that made us successful, and where we're going.
  • It's easy to read a job post and apply, but people often wonder about the culture and whether they would fit in.
  • If you want to call Harrow your home and genuinely want to be part of a family and something big, then we encourage you to click this link and get to know us.
  • Who is Harrow?

This listing is sourced directly from Harrow, Inc.'s careers page and normalized into a canonical job model.