Our client is a pharmaceutical and related health care products company whose mission is to extend and enhance human life. Our client seek an experienced Clinical Trial Associate based in their Belgium office to support clinical trials on a full time^basis for 12 months. You must already be based in Belgium and have excellent written and spoken English, Dutch, French.
Duties include:
Sending site surveys to sites. Preparing confidentiality agreements. Sending protocol packages to sites.Tracking & indexing country specific essential documents. Assisting the site manager with the preparation of EC submissions. IMPACT & GID maintenance. Preparing on-site investigator & materials for site initiation visit. Resupplying sites with studymaterials (e.g. CRFs). Liasing with sites to chase essential documents, CRF pages, queries, CTP documents. Processing and tracking investigator payments (liasing with local purchasing to add/maintain vendors). Co-ordinate regular mailings to sites. Providing site monitor & manager support. Filing & archiving.
Skills and Requirements:
Solid years of CTA experience within a pharma or CRO
Excellent written and spoken English, Dutch, French.
Knowledge of IMPACT and indexing into an Electronic study file would be beneficial
Excellent communication skills. Problem solving, winning attitude, self-motivated, ability to work independently, proactive, ability to multi-task and prioritise workload
Will be required to work across therapeutic^areas
Microsoft office experience (Word, Excel, Powerpoint)