Clinical Trial Assistant
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Devam ederek şunları kabul etmiş olursunuz: Şartlar & Gizlilik Politikası.
Responsibilities:
• Clinical supply & non‐clinical supply management, in collaboration with other country roles
• Collate, distribute/ship, and archive clinical documents
• Manage Labeling requirements and coordinate/sign translation change request
• Prepare documents and correspondence
• Ensure collection and distribution of study tools and documents
• Update clinical trial databases (CTMS) and tracker
• Assist with eTMF reconciliation
• Document proper destruction of clinical supplies.
• Execute eTMF Quality Control Plan Qualifications (Minimum Required):
• University or college degree (biological or life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology).
• Understanding of ICH-GCP guidelines.
• Understanding of the clinical trial process. Experience (Minimum Required):
• A minimum of 1.5 years of industry experience in a related role (e.g., IHCRA, CTA, Supply CTA ).
• Experience in clinical research supply management processes preferred.
• Good planning, organization, time management and problem-solving skills.
• Good communication skills, oral and written.
• Works efficiently and effectively in a matrix environment. #LI-CB1 #LI-Remote Learn more about our EEO & Accommodations request here.
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