R&D
Là où votre curiosité fait avancer les miracles de la science

• Job title: Trial Disclosure Manager (TDM)

• Location: Budapest, Hungary

• Job type: Permanent, full-time

• Hybrid working
  

About the job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Join our global Clinical Documentation team as a Trial Disclosure Manager and you’ll ensure timely public disclosure of protocol information and study results, in line with regulatory requirements and Sanofi data sharing commitments. You’ll work closely with clinical, statistics, regulatory, medical marketing, patents and pharmacovigilance colleagues, in order to get the best solutions to specific public disclosure challenges on behalf of Global Business Units while ensuring timeliness and quality of deliverables.   

Main responsibilities:

• Works with colleague TDMs, study and/or project teams, in order to plan, prepare, and release registrations and results on appropriate website/s within the required timelines.    As well, participates or leads activity in related process areas such as redaction of documents, preparation of summaries, management of public queries and others.

• Collaborates with colleagues and teams to drive resolution of specific disclosure challenges that may arise during product development and/or in relation to therapeutic specificities.

• Identifies and follows up CAPA in the event of deviations, for the assigned therapeutic or product area/s.

• Supervises consultant and/or vendor/s on selected disclosure activity, ensuring in partnership the timely production of high-quality deliverables for Global Business Units or other Customers.

• Participates in / contributes to / leads selected quality, technical, and/or process-driven activities in order to ensure complete and timely follow up of the defined deliverables.

• Trains or participates in delivery of selected training of colleagues, or Vendor, and similar communications.

• Has or develops knowledge of disclosure regulations, website standards, and company commitments / policy, and applies them appropriately in order to guide study, project teams, and colleagues, through appropriate communications. 

About you

Experience:

•          Understanding of or exposure to the clinical development environment

Soft Skills:

•          Ability to summarize scientific information and edit text for specific audiences

•          Quality consciousness, attention to detail, and an inquisitive mindset

•          Good sense of organization, prioritization, adaptability

•          Excellent interpersonal and ‘relational/oversight’ skills, team-player

Technical skills: 

•          Ability to summarize scientific information and edit text for specific audiences

•          Comfortable with computer applications and ongoing innovations

Education: 

• Scientific background (master’s degree, or equivalent professional experience)

Language(s):

• Strong English skills (verbal and written), ability to exchange fluently in a global environment

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team in an international work environment

• Work from an "Office of the Year 2023" award winner with flexible home office policy

• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact

• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave

• An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks

• Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)

PursueProgress. Discover Extraordinary.

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Discover our Code of Conduct, that serves as the moral compass that guides us when chasing the miracles of science to improve people’s lives. Please ensure to have read this document before applying.

#Sanofi #SanofiCareers #joinSanofi

#jobopportunities #careeropportunities #sscjob

#Sanofi_Budapest_Hub #Budapest

#R&D

#LI-EUR #LI-hybrid

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Toujours Progresser. Découvrir l’Extraordinaire.

Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.

Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.