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EXTEDO is of the leading names in the field of Regulatory Information Management (RIM). With our EXTEDOpulse solutions and expert consultants, we are on a mission to enable agencies and life sciences organizations around the world to bring new products to market faster and safer. EXTEDO enables more than 35 regulatory authorities and over 1000 maintained customers across 65 countries to deliver Effortless Compliance. Our clients range from small CROs to large multi-national pharmaceutical organizations. The areas of Life Sciences in which EXTEDO operates are: pharmaceuticals, biotech and biopharma, generics, medical devices, healthcare and the public sector. We are still growing!

For our location in Ottobrunn near Munich or in remote we are actively seeking a

Senior Business Consultant RIMS (m/f/d)


Aufgaben
  • Provide RIMS specific consulting internally at EXTEDO and directly to the company's clients
  • Drive business consulting activities for EXTEDO's software integrating the company's Products into the business processes
  • Create consulting plan, identify and evaluate subject domain gaps, and propose optimizations in business operations of EXTEDO clients
  • Contribute to RFPs, RFIs and SoWs for end services
  • Edit, update and review of relevant documentations and processes
  • Perform consulting workshops with customer as part of presales or project activities
  • Participate in services development activities to extend the EXTEDO offering portfolio
  • Run webinars, present at conferences, and participate in global events to promote the EXTEDO footprint
  • Report project-related activities to the respective project manager and keep track in the EXTEDO time tracking system
  • Work closely with Sales, Development and Support teams to provide the best solution for our customers

Profil
  • A completed degree in computer sciences or a domain specific degree (e.g. life science, regulatory) or another comparable qualification
  • 5-years of practical project experience in the field of business consulting or equivalent exposure in a pharma/CRO setting
  • Project Management experience gained either by having acted as project manager or by participating in project teams
  • Client oriented with excellent analytical and problem-solving skills
  • Advanced knowledge in RIMS/IDMP systems and processes is a must. Cross-domain knowledge in more than one field will be highly appreciated (Regulatory, Submissions, QA, Pharmacovigilance, Clinical Trials).
  • Very good organizational, presentation and communication skills put forth in a professional and business appropriate manner
  • Basic understanding of IT architectures, technical Computer System Validation, and core processes (e.g. Migrations, Databases)
  • Willingness to travel to customers worldwide
  • Excellent English skills (spoken and written), second language is a plus

Wir bieten
  • 30 Days Vacation
  • Home Office
  • Personal Development
  • Pension Scheme
  • Overtime Regulation
  • Flexible Working Hours
  • Canteen
  • Free Coffee & Tea