14 дней назад
Associate Medical Director, Nephrology
241 800 - 513 900PLN
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Medical Director, Nephrology (Clinical Research): Providing medical, clinical, and scientific oversight for nephrology clinical trials with an accent on medical monitoring, protocol review, and patient safety. Focus on reviewing adverse events and clinical study reports, advising investigative sites and project teams, and supporting early clinical development activities.
Location: Warsaw, Poland; regular travel of 15–20% may be required.
Annual base pay: PLN 241,800–513,900.
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Act as a Global Medical Advisor and Scientific Advisor on assigned clinical research projects.
- Provide medical guidance to project leaders, investigative sites, and clinical project staff on protocol, patient safety, and eligibility matters.
- Review protocols, Investigative Drug Brochures, Case Report Forms, adverse events, and adverse event coding.
- Support Serious Adverse Event reviews and Analysis of Similar Events in collaboration with Pharmacovigilance.
- Deliver therapeutic-area training and participate in Investigator, kick-off, project, and client meetings.
- Review Clinical Study Reports and patient narratives, and provide urgent protocol-related support when required.
Requirements
- Medical degree from an accredited, internationally recognized medical school and a medical license or equivalent in the country or region of residence and work.
- At least 5 years of clinical medicine experience plus clinical trials experience as an investigator or in the pharmaceutical, CRO, or biotech industry.
- Current knowledge of the scientific, clinical, regulatory, commercial, and competitive landscape in the applicable therapeutic area.
- Knowledge of federal and local clinical research regulations and guidelines; board certification required.
- Experience or knowledge in Phase I studies or early clinical development.
- Fluent English required.
Culture & Benefits
- Full-time position with potential incentive plans, bonuses, and other compensation depending on the position offered.
- Health, welfare, and other benefits may be provided.
- Availability for urgent protocol-related questions may be required 24/7 in accordance with local labor laws.
- Work includes collaboration across medical, clinical, project, Pharmacovigilance, and client-facing teams.
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