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5 часов Π½Π°Π·Π°Π΄

Associate Director, Clinical Scientist (Ophthalmology)

154Β 500 - 195Β 700$
Π€ΠΎΡ€ΠΌΠ°Ρ‚ Ρ€Π°Π±ΠΎΡ‚Ρ‹
remote (Ρ‚ΠΎΠ»ΡŒΠΊΠΎ USA)
Π’ΠΈΠΏ Ρ€Π°Π±ΠΎΡ‚Ρ‹
fulltime
Π“Ρ€Π΅ΠΉΠ΄
senior
Английский
b2
Π‘Ρ‚Ρ€Π°Π½Π°
US
Вакансия ΠΈΠ· списка Hirify.GlobalВакансия ΠΈΠ· Hirify Global, списка ΠΌΠ΅ΠΆΠ΄ΡƒΠ½Π°Ρ€ΠΎΠ΄Π½Ρ‹Ρ… tech-ΠΊΠΎΠΌΠΏΠ°Π½ΠΈΠΉ
Для мэтча ΠΈ ΠΎΡ‚ΠΊΠ»ΠΈΠΊΠ° Π½ΡƒΠΆΠ΅Π½ Plus

ΠœΡΡ‚Ρ‡ & Π‘ΠΎΠΏΡ€ΠΎΠ²ΠΎΠ΄

Для мэтча с этой вакансиСй Π½ΡƒΠΆΠ΅Π½ Plus

ОписаниС вакансии

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TL;DR
Associate Director, Clinical Scientist (Ophthalmology): Supporting global clinical development programs and registrational strategies for retinal disease therapies with an accent on ophthalmology, clinical trial documentation, safety review, and regulatory submissions. Focus on analyzing clinical data, ensuring ICH/GCP compliance, supporting trial recruitment and site initiation, and preparing materials for health authority interactions.

Location: Remote within the United States; office address listed in Watertown, Massachusetts.

Salary: $154,500–$195,700 USD per year.

Company

hirify.global is an ophthalmology company developing and commercializing innovative therapeutics for serious retinal diseases and blindness prevention.

What you will do

  • Support the implementation of clinical development plans and registrational strategies for assigned products.
  • Collaborate with clinical development teams and CROs on protocols, investigator brochures, informed consent templates, case report forms, procedure manuals, and clinical study reports.
  • Review and analyze clinical trial data, including safety, effectiveness, protocol adherence, interim analyses, and statistical analysis plans.
  • Prepare clinical documents and briefing materials for global health authority meetings and regulatory submissions.
  • Support site initiation activities, monitoring plans, investigator meetings, and required trial documentation.
  • Assist with recruitment strategies, enrollment tracking, study milestones, and metrics while ensuring global trials follow ICH, GCP, and regulatory requirements.

Requirements

  • Advanced degree in a life science, clinical, or medical field; PhD or PharmD preferred.
  • Minimum of 5+ years of clinical development, clinical research, and R&D experience preferred for the Associate Director level.
  • Strong understanding and application of clinical research procedures and Good Clinical Practice standards.
  • Experience in ophthalmology and familiarity with drug/device combination products.
  • Experience across clinical drug development phases, including regulatory submissions.
  • Strong communication, organizational, interpersonal, analytical, and independent decision-making skills, with experience in cross-functional matrix teams.

Culture & Benefits

  • Remote work arrangement.
  • Work focused on developing vision-preserving treatments for patients with serious retinal diseases.
  • Culture emphasizes transformational innovation, integrity, compassionate excellence, and inclusive collaboration.
  • Commitment to diversity, inclusion, and equal employment opportunity.

Π‘ΡƒΠ΄ΡŒΡ‚Π΅ остороТны: Ссли Ρ€Π°Π±ΠΎΡ‚ΠΎΠ΄Π°Ρ‚Π΅Π»ΡŒ просит Π²ΠΎΠΉΡ‚ΠΈ Π² ΠΈΡ… систСму, ΠΈΡΠΏΠΎΠ»ΡŒΠ·ΡƒΡ iCloud/Google, ΠΏΡ€ΠΈΡΠ»Π°Ρ‚ΡŒ ΠΊΠΎΠ΄/ΠΏΠ°Ρ€ΠΎΠ»ΡŒ, Π·Π°ΠΏΡƒΡΡ‚ΠΈΡ‚ΡŒ ΠΊΠΎΠ΄/ПО, Π½Π΅ Π΄Π΅Π»Π°ΠΉΡ‚Π΅ этого - это мошСнники. ΠžΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΠ½ΠΎ ΠΆΠΌΠΈΡ‚Π΅ "ΠŸΠΎΠΆΠ°Π»ΠΎΠ²Π°Ρ‚ΡŒΡΡ" ΠΈΠ»ΠΈ ΠΏΠΈΡˆΠΈΡ‚Π΅ Π² ΠΏΠΎΠ΄Π΄Π΅Ρ€ΠΆΠΊΡƒ. ΠŸΠΎΠ΄Ρ€ΠΎΠ±Π½Π΅Π΅ Π² Π³Π°ΠΉΠ΄Π΅ β†’