Product Designer, Remote in Latvia
MWDN
Own product features from discovery through implementation for an Israeli online cyber defense company. Design complex SaaS workflows, dashboards, responsive interfaces, and reusable Figma components.
Deschide
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.
Clinical Trial Coordinator
Support ICON’s sponsor-dedicated clinical research operations by helping monitor U.S. trial sites remotely. Assist with trial documentation, compliance, site reporting, and team coordination.
Descriere
- Help monitor clinical trial sites for compliance with study protocols, regulations, and Good Clinical Practice (GCP) guidelines.
- Prepare site documents, enter data, and track site performance measures.
- Coordinate with cross-functional colleagues to share information and resolve site issues.
- Keep site activity records accurate and help prepare monitoring reports.
- Take part in training to build clinical trial management knowledge and skills.
- Work with the team and stakeholders to deliver high-quality clinical research.
Cerințe
- Hold a bachelor’s degree in a relevant area, such as life sciences, healthcare administration, or clinical research.
- Experience in clinical research, site management, or a related administrative role is preferred but not required.
- Have strong organizational skills and attention to detail, with the ability to manage several tasks effectively.
- Knowledge of clinical trial processes and regulatory requirements is an advantage.
- Bring strong communication and interpersonal skills and the ability to work well with a team.
- Be willing to travel as needed, approximately 25% of the time.
- Have legal authorization to work in the country where the role is based.
Beneficii
- Base salary with performance-related incentives.
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programs and wellbeing resources.
- Structured training and career pathways for learning and development.
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