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
- Support the processing of safety cases from clinical trial and post‑marketing sources , including AEs, SAEs, and SUSARs.
- Assist with case receipt, triage, data entry, MedDRA and WHO Drug coding, follow‑up activities, and quality checks within safety databases.
- Support expedited and local ICSR submissions under supervision.
- Assist with reconciliation of safety data with clinical databases .
- Support global and local literature monitoring activities.
- Maintain and update Drug Safety documentation, trackers, and project files in line with internal procedures.
- Provide administrative and operational support to the Global Drug Safety team, including mailbox monitoring and document management.
- Support compliance monitoring, reporting activities, and internal process adherence.
- Collaborate with cross‑functional teams and external partners as required.
Koho hledáme
- Bachelor’s degree in pharmaceutical sciences, life sciences, medicine , or a related field.
- 1–3 years of experience in Drug Safety, Pharmacovigilance, or a medical environment, including case processing and regulatory submissions.
- Experience in safety case processing within both clinical trial and post‑marketing settings is required.
- Basic understanding of Drug Safety regulations and guidelines, including ICH, GVP, GCP, and CIOMS.
- Experience or familiarity with safety databases is an advantage.
- Fluent written and spoken English.
- Strong attention to detail, organizational skills, and willingness to learn.
- A collaborative team player with a positive and proactive attitude.
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.
