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6 дней назад

Senior Clinical Research Associate

Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Poland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
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TL;DR
Senior Clinical Research Associate (Clinical Trials): Advancing clinical research by managing investigative site relationships, monitoring trial conduct, and ensuring data integrity, compliance, and patient safety with an accent on site engagement, risk-based monitoring, and regulatory requirements. Focus on identifying and mitigating site risks, improving recruitment and retention, mentoring CRAs, and maintaining audit and inspection readiness.

Location: Warsaw, Poland

Company

hirify.global develops innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Act as the primary sponsor contact for investigative sites and coordinate engagement with study teams, investigators, and site staff.
  • Evaluate, train, and monitor clinical trial sites through on-site and off-site activities, including site initiation and closure.
  • Support protocol execution, patient recruitment and retention, data quality, safety reporting, and overall study performance.
  • Conduct continuous risk assessments, resolve site risk signals, and implement preventive and corrective action plans.
  • Identify and assess potential investigators and sites, manage site relationships, and support investigator payments where applicable.
  • Mentor junior CRAs and contribute to local onboarding, task forces, and clinical research initiatives.

Requirements

  • At least 3 years of clinically related experience, including preferably 2 years of independent monitoring of investigational drug or device trials.
  • Health-related tertiary qualification, such as medicine, science, pharmacy, or nursing, preferred.
  • Knowledge of therapeutic areas, clinical trial execution, risk-based monitoring, local regulatory requirements, ICH/GCP guidelines, and applicable policies.
  • Advanced communication, collaboration, planning, organizational, interpersonal, and critical-thinking skills.
  • Excellent command of English and the local language required.
  • Ability to work independently, manage competing deadlines, use clinical research technologies, and maintain integrity and quality standards.

Culture & Benefits

  • Work focused on turning scientific research into medicines and improving patient outcomes.
  • Collaboration with internal R&D stakeholders, investigators, and clinical site personnel.
  • Opportunities to mentor colleagues and participate in global and local initiatives.
  • Commitment to integrity, innovation, community service, and equal employment opportunity.

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