6 дней назад
Senior Clinical Research Associate
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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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