Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Experience in pharmacovigilance or drug safety is preferred., Strong analytical and communication skills are essential., Familiarity with regulatory requirements and safety reporting processes..

Key responsibilities:

Monitor and evaluate adverse drug reactions and safety data.

Prepare and submit safety reports to regulatory authorities.

Collaborate with cross-functional teams to ensure compliance.

Conduct risk assessments and contribute to safety management plans.

Arriello is a leading life sciences consultancy, offering expert guidance in regulatory affairs, pharmacovigilance and quality compliance. Our global services span the product lifecycle from clinical to post-submission regulatory affairs, pharmacovigilance, and quality & compliance. Headquartered in Ireland and with operations across Europe, we provide services and solutions globally. With decades of experience, ISO:9001 certification, and a friendly, diverse team, we‘ve been a trusted partner to the life sciences industry, primarily with pharmaceutical and biotech companies since 2008.

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