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Regulatory Submission Specialist
Marketing
Publicis Le Pont

Regulatory Submission Specialist

Publicis Le Pont
Warszawa
Rodzaj pracy
Pełny etat
Doświadczenie
Specjalista/Mid
Forma zatrudnienia
Umowa o pracę
Tryb pracy
Praca Hybrydowa
Publicis Le Pont
Publicis Le Pont

Publicis Groupe to największy holding reklamowy, lider w dziedzinie marketingu, komunikacji, transformacji cyfrowej.

Zobacz profil pracodawcy
Wymagane umiejętności
Microsoft Excel
pharmaceutical marketing
regulatory affairs
Adobe Acrobat
Microsoft Word
PowerPoint
Attention to details
Veeva Vault
Friendly offer
Opis stanowiska

As a Regulatory Submission Specialist, you will be responsible for researching medical documents, finding the correct references for pharmaceutical marketing assets, submitting this content into Veeva Vault platform and maintaining internal processes and project management. The role will be perfect for you if you have strong organizational and coordination skills, and a desire to work in a collaborative team environment. You should be able to work well in a rapidly changing, dynamic environment, and have excellent written and verbal skills.


  • Researching medical documents to reference digital marketing assets for Medical, Legal and Regulatory (MLR) review.
  • Liaising with cross-functional team members, specifically project managers to ensure there are clear communication lines and escalation pathways.
  • Submitting materials into Veeva Vault and submission platforms.
  • Adding any applicable annotations to submissions.
  • Ensuring timely submission of materials.
  • Maintaining familiarity with industry standards to ensure that documents meet or exceed regulatory requirements and guidance.
  • Monitoring timelines for assigned projects and updating the Program Leads if deliverables are at risk.
  • Reviewing and forwarding feedback from MLR team to internal Production teams for amendments.
  • Contributing to the development of process improvement tools and revisions of internal policies and procedures affecting submissions.


Qualifications:

  • Min. Bachelor’s degree in pharmaceutical or medical sciences.
  • 1-2 years of pharmaceutical marketing or regulatory affairs experience.
  • Ability to understand and absorb scientific content, follow established timelines, expectations, priorities and objectives. Critical thinking.
  • Proficiency with various applications including Adobe Acrobat, Microsoft word, Excel, and PowerPoint.
  • Exercises good judgement with defined procedures and policies to determine appropriate action. Strong attention to details and accuracy in work.
  • Proactive team player with strong interpersonal skills. Takes ownership and drives positive, collaborative results.
  • Excellent written and verbal communication, planning and organizational skills.
  • Ability to work under pressure, solutions oriented. Versatile and comfortable in a multitasking environment.
  • Knowledge of Veeva Vault platform.


We offer the following:

  • Opportunity to develop in a stable company with an established position in the market.
  • Extensive range of online training courses in cooperation with reputable market partners.
  • Opportunity to participate in international and local development projects and programmes.
  • International working environment.
  • Attractive package of non-wage benefits (medical care, the Nais benefit platform, recreation allowance, access to a platform for learning foreign languages, access to the Marcel international training platform, etc.).
  • High working flexibility (we work in a hybrid model, with predominance of home office).
  • Work Your World – opportunity to work from any place in the world for 6 weeks a year and access to the Home Swap Home internal platform.
  • Friendly and casual working atmosphere in a close-knit team filled with positive energy.


At Publicis Groupe, we value diversity and invite all candidates to apply, regardless of age, gender, sexual orientation, religion or lack thereof, origin or disability.

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