O pozici
At Arriello , we provide Pharmacovigilance, Quality & Compliance, and Regulatory Affairs services to global pharmaceutical and life sciences companies, helping them meet regulatory requirements and protect patient safety.
We are a growing business with a collaborative culture focused on high‑quality delivery, continuous improvement, and giving people the space to do their best work.
Our values guide how we work:
Inclusive – We value fairness, respect, and learning from one another
Dedicated – We deliver practical, client‑focused solutions
Innovative – We work together to find better ways forward
Passionate – We build strong relationships and care about the quality of what we do
Co budeš dělat
- Provide strategic leadership and oversight of global PV operations, including case management and end‑to‑end safety processes
- Ensure compliant, high-quality, and timely processing of safety data in line with global regulatory requirements
- Drive operational excellence through continuous improvement, automation, and process optimisation initiatives
- Lead organisational transformation, including outsourcing strategies and technology adoption to enhance efficiency and scalability.
- Oversee PV vendors and partners, ensuring performance, quality, and compliance standards are met.
- Establish and monitor KPIs, dashboards, and performance metrics to support data-driven decision making.
- Collaborate with cross-functional stakeholders including Clinical, Regulatory, Medical Affairs, Quality, and IT.
- Ensure inspection readiness and support audits and regulatory inspections globally.
- Build, lead, and develop a high-performing PV operations team, fostering a culture of excellence and accountability.
Koho hledáme
- Extensive experience in pharmacovigilance / drug safety within the pharmaceutical or biotech industry
- Proven leadership experience managing global PV operations and teams
- Strong knowledge of global PV regulations (e.g. FDA, EMA, ICH, GVP)
- Experience in case processing, safety systems, and vendor management
- Track record of driving process improvement, transformation, and operational efficiency
- Excellent stakeholder management and communication skills
- Degree in Life Sciences, Pharmacy, Medicine, or related field (advanced degree preferred)
Benefity
- Work remotely while contributing to a global life sciences consultancy .
- Lead quality operations that directly influence patient safety and regulatory compliance.
- Collaborate in a multicultural, inclusive, and innovative environment.
- Enjoy opportunities for career progression, professional development, and international exposure.
- Flexible Work Options : Remote working flexibility to support your lifestyle.
- Generous Time Off: Enjoy 5 weeks of holiday plus national holidays and 3 personal days to recharge.
- Home Office Support: Get support to create a productive home office setup.
- Bonuses: Benefit from an annual bonus program, spot bonuses, and employee-nominated recognition.
