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4 дня назад

Senior Clinical Trials Manager (Biotech)

143 000 - 157 300$
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
Senior Clinical Trials Manager (Biotech): Managing global clinical studies, study-site activities, clinical documents, and patient data monitoring with an accent on protocol interpretation, safety compliance, and cross-functional coordination. Focus on supporting site recruitment and training, maintaining regulatory and treatment data, and improving SOPs and clinical-trial execution processes.

Location: Remote or onsite in El Segundo, California, as specified in the offer letter; approximately 20% travel required.

Annual base pay: $143,000–$157,300 for the national market or $150,000–$165,000 for premium markets, depending on qualifications, experience, and geographic location. Eligible for a discretionary bonus and equity award.

Company

Develops immunotherapies, cell therapies, cancer vaccines, and infectious-disease treatments designed to activate and strengthen the natural immune system.

What you will do

  • Manage activities across several global, company-sponsored clinical studies with support from the Clinical Project Manager.
  • Develop and maintain informed consents, laboratory and pharmacy manuals, case report forms, and other study execution documents.
  • 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.
  • Maintain patient treatment, response, and survival data and prepare clinical-trial updates.
  • Improve and standardize SOPs, templates, and clinical development processes.

Requirements

  • Bachelor’s degree and 7+ years of relevant clinical research experience.
  • Experience supporting global clinical trials, clinical sites, study documents, and patient data monitoring.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Excellent written and verbal communication, organization, and multitasking skills.
  • Ability to follow company SOPs, maintain confidentiality, work in a standard office or in-lab environment, and lift up to 20 pounds.

Culture & Benefits

  • Collaborative environment with opportunities to work across different areas of the company.
  • Professional development opportunities within a growing publicly traded biopharmaceutical company.
  • Medical, dental, and vision plan options, health and financial wellness programs, and an employee assistance program.
  • Life, disability, flexible spending, legal, identity-theft, pet-insurance, and employee-discount benefits.
  • 401(k) retirement plan with company match, 529 education savings program, paid holidays, and paid time off.

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