Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functions—underpinned by the world’s largest delivery network—Accenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 373,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at www.accenture.com.
Accenture Operations is one of Accenture key capabilities dedicated to work on outsourcing engagements. These are long-term partnerships with clients for whom we manage and provide increasingly specialized business operations, such as finance and accounting, IT, applications development and maintenance, helpdesk services, and HR. We not only maintain key business functions for clients, we constantly seek to improve them to help our clients move ahead of the competition.
Accenture’s Accelerated R&D Services bring a fully integrated, robust business service that delivers enhanced processes across the Clinical, Regulatory and Pharmacovigilance (PV) functions around the globe. Our solutions, supported by outsourced operational activities and facilitated by customizable technology and infrastructure, allow pharmaceutical companies to bring drugs to market faster, at a reduced cost and with reduced execution risks.
Your future is waiting – just make a step forward!
Would you love to work with passionate people from all over the world?
Are you dreaming about using your foreign language skills and at the same time gaining knowledge?
Take a just one look and decide if Accenture is a place for You!
- Coordinate submission documentation (new and lifecycle submissions). Leverage publishing team as appropriate.
- Review and validate submission technical.
- Coordinate final submission review and approval by appropriate stakeholders.
- Finalize and dispatch submission to client affiliates or Health Authorities as required.
- Create and maintain initial and life cycle events in regulatory information management (RIM) system.
- Experience in publishing of regulatory submissions for Investigational (IND, CTA) or Marketing Applications (NDA, MAA, NDS, MAA, 510k) to Health Authorities in eCTD, NeeS, eSub or paper formats.
- Knowledge of regulatory submission requirements and understanding of the nuances of different submission components.
- Experience with publishing software and tools used throughout the pharmaceutical industry and in regulatory information management (RIM) systems.
- Minimum 2 years of experience in an area of expertise (e.g., regulatory documentation publishing, RIM data management).
- Knowledge in handling registrations and maintenance of pharmaceutical products from a regional or local perspective.
- The ability to use your knowledge of foreign language on a daily basis at work (we serve our Clients in almost 30 foreign languages).
- Experience with a range of Clients and technology solutions which provides professional relevance.
- Operating according to Lean Six Sigma philosophy.
- Collaborating and learning from diverse and talented colleagues helps you “raise your game”.
- Trainings and development tailored to help you achieve your potential.
- New Joiners Programme including trainings.
- Opportunity to engage in Corporate Social Responsibility initiatives.
- We also think about your social life, at Accenture you will be able to take part in different initiatives like Book Club, International Cuisine Club, Accenture Runners Club, family events, cultural meetings, photography classes, climbing, soccer, swimming and many others.
- Social benefit packages including: private medical care, Sodexo vouchers, Benefit sport club cards, life insurance.
- Friendly work atmosphere in multicultural environment.