ICON plc

Asistență medicală Consultanță Logistică

ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.

Locurile de muncă ale companiei

Clinical Trial Associate – Hybrid, Mechelen

Support the coordination, documentation, and reporting of clinical trials for ICON’s sponsor-dedicated pharmaceutical programs. This hybrid full-time role is based in Mechelen, Belgium, with a mix of office and home working.

acum 6 zile

Belgia Hibrid Normă întreagă Junior Nivel mediu Limbă Obligatorie: engleză Asociat pentru studii clinice General

Descriere

Coordinate and administer clinical trials in line with study protocols and regulatory requirements
Organize and maintain study files, essential documents, and regulatory submissions
Help prepare study materials, including informed consent forms and case report forms
Collaborate with cross-functional teams to support communication and effective trial delivery
Track clinical trial milestones and metrics and contribute to related reporting
Support sponsor-dedicated work through ICON’s global clinical research expertise
Contribute to the work of a global, science-led, patient-focused pharmaceutical company with offices in the Brussels region

Cerințe

Bachelor’s degree in a scientific or healthcare-related discipline
Previous clinical research experience or a strong interest in the field
Understanding of clinical trial procedures, regulations, and guidelines
Strong organizational and communication abilities
Collaborative approach, with close attention to detail in a fast-paced setting
Legal authorization to work in the country where the position is located

Beneficii

Base salary with performance-related incentives
Health and wellbeing programmes, including medical, dental, and vision coverage where applicable
Retirement and pension arrangements
Life assurance and disability cover
Employee assistance programmes and wellbeing resources
Structured training and career development opportunities

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Clinical Trial Associate – Hybrid, Mechelen

Support the coordination, documentation, and reporting of clinical trials for ICON’s sponsor-dedicated pharmaceutical programs. This hybrid full-time role is based in Mechelen, Belgium, with a mix of office and home working.

Descriere

Cerințe

Beneficii

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