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6 дней назад

Clinical Trials Manager (Biotech)

130 000 - 143 000$
Формат работы
remote (только USA)/onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Trials Manager (Biotech): Managing company-sponsored clinical studies, clinical site activities, study documents, and patient treatment and response data with an accent on protocol interpretation, safety compliance, and regulatory coordination. Focus on supporting site recruitment and training, leading DSMB and investigator teleconferences, and maintaining clinical trial updates across active studies.

Location: Dunkirk, New York, United States; onsite or remote depending on the candidate's geographic location. Monday–Friday during standard business hours, with approximately 20% travel and exposure to an in-lab environment.

Annual base salary: $130,000–$143,000 for the national market; premium-market range of $136,500–$150,000. The role is also eligible for a discretionary bonus and equity award.

Company

hirify.global is a publicly traded biotechnology company developing immunotherapies, cell therapies, cancer vaccines, and infectious-disease treatments designed to harness the immune system.

What you will do

  • Manage activities across several company-sponsored clinical studies and support clinical trial execution.
  • Develop and maintain study documents, including informed consents, laboratory and pharmacy manuals, case report forms, and other execution tools.
  • Support site recruitment, initiation, payments, close-out, staff training, and protocol-amendment training.
  • Guide clinical sites on protocol interpretation and safety compliance while coordinating updated regulatory documentation.
  • Lead or moderate DSMB, principal investigator, and study coordinator teleconferences.
  • Maintain patient treatment, response, survival, and clinical trial update data for active studies.

Requirements

  • Bachelor’s degree in biological science and 5+ years of relevant clinical research experience.
  • Experience supporting clinical trials, clinical sites, study documentation, and patient data monitoring.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Excellent written and oral communication, organization, and multitasking skills.
  • Ability to follow company SOPs, maintain confidentiality, work in a standard office and laboratory environment, and lift up to 20 pounds.

Culture & Benefits

  • Collaborative environment with opportunities to work across different company areas.
  • Professional development opportunities within a growing biopharmaceutical company.
  • Medical, dental, and vision plan options, health and financial wellness programs, and an employee assistance program.
  • Life, accidental death and dismemberment, short- and long-term disability, healthcare and dependent-care flexible spending accounts, and a 401(k) with company match.
  • Paid time off, holidays, education savings, legal services, identity theft protection, pet insurance, and employee discounts.

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