Om uw bezoek aan onze website te verbeteren maken wij gebruik van cookies. Het voortzetten van uw websitebezoek zien wij als goedkeuring voor het plaatsen en gebruiken van cookies op uw computer.
Meer informatie vindt u in de Cookies-sectie van onze Privacyverklaring.
OK

Data Manager

Region of Antwerpen, Belgium

Core Purpose of Role: The Data Manager is a functional expert in the field of Clinical Research Data Management (DM), and as such supports the Clinical Study Team (CST) through managing the collection, review and reporting of clinical data and related activities during the planning, set-up, conduct, and close-out of clinical trials.

Uw verantwoordelijkheden

Principal Accountabilities:


• Participate in CST meetings as DM representative, and closely interact with Biostatistics, Medical, Clinical Operations and other functional representatives
• Provide data management expertise during protocol development, including for any amendments
• Coordinate DM Contract Research Organization (CRO) Request for Proposal (RfP) selection process, create necessary Purchase Order (PO) Requests and follow up on related Goods Receipt (GR)
• Act as first point of contact for DM CRO counterparts and ensure clinical study data management deliverables within agreed budget and timelines, and with high quality (complying with company processes, ICH-GCP and applicable regulations and guidelines)
• Organize relevant data management oversight meetings and ensure minutes are documented
• Create and maintain Data Management Oversight Plan and ensure proper execution of necessary quality control steps
• When company InForm is used, ensure necessary steps are taken to get DM CRO started, and provide further support where needed
• Ensure proper and timely filing of DM-specific documents and files in Trial Master File or other secured dedicated environment
• Actively participate in DM and Biometrics team meetings
• Adhere to relevant policies and procedures and ensure timely completion of relevant training
• Interact with Quality & Compliance to follow up on audit and inspection reports and assigned Corrective Action/Preventive Action plans in timely manner; participate in audits and inspections where needed
• Lead or contribute to Process Improvement initiatives as required

Uw Profiel

• Proven experience in Data Management and with described duties
• Life Sciences background
• English at great level

Deze omschrijving komt overheen met uw profiel en verwachtingen?

Vacatures overzicht