Offer summary

Qualifications:

Bachelor's degree in Pharmacy, Life Sciences, or related field., Experience in pharmacovigilance or drug safety is preferred., Strong analytical skills and attention to detail are essential., Excellent communication skills in both English and Greek..

Key responsabilities:

Monitor and report adverse drug reactions and safety data.

Collaborate with healthcare professionals and regulatory authorities.

Ensure compliance with local and international pharmacovigilance regulations.

Provide training and support to staff on safety reporting procedures.

Excelya Germany GmbH, formerly Koehler eClinical GmbH (www.koehler-eclinical.com), part of Excelya group (www.excelya.com) is a medium size full-service CRO with more than 25 years experience in providing value-added services for our customers. With a strong heritage in biostatistics, we are covering all study phases as well as biostatistical and regulatory consulting, meta-analyses, data integrations and -standardizations. As specialist for data-centric approaches, the company operates its proprietary software VITESSA as a combined tool for EDC and clinical trial management. We provide full service support for local and global trials with centralized project management and technology-enabled approaches for early as well as late-phase projects, including NIS, observational and PASS.

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