Director (m/f/d) Therapy Area Head, Global Regulatory Medical Writing

We want to improve the life of our patients. That is our daily mission. We are proud of our 2,900 employees who provide millions of people with essential medicines every day. Health needs a healthy environment - we are committed to this and, as an environmental pioneer in the German pharmaceutical industry, we set our German sites carbon-neutral in 2021. 

And that's not all: we are represented We want to improve the life of our patients. in over 60 countries worldwide, the market leader in generics and the home of Germany's well-known pharmaceutical brand ratiopharm. As a full-service provider, we offer a wide range of approximately 3,500 products. These includes innovative medicines, generics, biosimilars and over-the-counter medicines. In our global network, we are constantly developing new, innovative therapies to further improve healthcare for all people. Several teams located at the German site are part of Global and European departments and thus contribute to Teva's success around the globe.

In a nutshell: We are Teva - and we are very proud of it

If you feel like us and if you are someone who enjoys exploring unknown paths - then we would like to get to know you. Are you also enthusiastic about global markets and pioneering technologies? And would you like to develop the future of healthcare at a leading provider of medicines? Fantastic Then become part of our team

Curious about the German site? Fantastic, then take a look:

This is a remote opportunity and candidate can sit anywhere in Germany.

A Director, in Global Regulatory Medical Writing, reports into Head of Global Regulatory Medical Writing, will primarily work in therapeutic area specific/functional role as a leader and SME representing GRMW in matrixed stakeholder R&D program teams. This role provides a significant level of oversight and SME guidance to internal medical writing team and cross-functional matrixed project teams in the strategic planning, scope determination and development of clinical and regulatory documents used in drug development and product registrations. The Director offers clear guidance, leadership, accountability for the preparation of quality, fit-for-use clinical regulatory documents for various regulatory and reporting purposes in an E2E business model.  As per business needs, may write and edit clinical regulatory documents, including submission summaries and other complex documents, as well as resource and budget management

• Primarily works on the therapeutic area/functional level 
• Likely to have direct reports; oversees contingent workers and/or vendors; provides training to others; strategically analyzes needs to manage resources and is accountable for resource allocation for therapeutic specific business needs with support from department head
• Oversees/provides guidance and accountable for all document types prepared by medical writers, review documents internally within medical writing function before stakeholder engagement, may write and edit clinical regulatory documents (all types) as per business needs
• Ensures that documents are fit-for-purpose, contains clear and consistent medical/scientific messaging that are accurate and complete, adheres to applicable regulatory guidelines, ICH guidance, and Teva standards 
• Leads/contributes to the preparation/revision of document templates 
• Participates in the recruiting/hiring process, development of direct reports including identifying learning/training opportunities, performance assessment and reviews 
• Responsible for tracking/providing team metrics and establish key performance indicators 

Required:

• PhD or PharmD in life sciences (or other related field) is preferred or Master's degree in life sciences (or other related field)
• PhD or Pharm D with a minimum of 8 years of experience Master's degree with minimum of 10 years of experience 

Functional Knowledge:

• Expert in all document types. Oversees/mentors for all document types at therapeutic area or functional level. 
• Guides/oversees medical writers; considered a proficient manager with regulatory medical writing expertise.
• Considered an internal expert in all aspects of regulatory medical writing and clinical drug development.
• Influences and potentially leads creation of regulatory medical writing processes and standards. Serves as subject matter expert for the Medical Writing function. 

Related Knowledge:

Knowledge of global regulations and guidelines for document submissions, and experienced in leading regulatory global submissions 

Job-Specific Competencies: 

• Excellent written and oral communication skills 
• Team player, dynamic, engaged, and agile to drive business needs and execute departmental vision at Teva
• Primary accountability is delivering high quality documents that are fit-for-use and within timelines with medical writing colleagues
• Represents MW in program teams providing leadership and guidance as an SME 
• Addresses business/program/project level issues; makes independent decisions using past experience and current situation to drive solutions and mitigate risks
• Persuades and inspires team to take action; coaches and mentors' junior medical writers and team as applicable to build MW SME presence, has expert negotiation skills
• Contributes to content preparation for departmental initiatives, participates in process development, and improvement cross-functionally with direction from department head
• Leads development of process, and preparation/revision of SOPs and guidance documents with department head and medical writing LT team
• Forecasts and maintains budget as per business needs and direction from department head

At Teva

• we take care of your health (among other things through a company health management system, a company doctor, physiotherapy, sports activities and a company canteen)
• you have time for your family (through our own company kindergarten and holiday camps for school children, as well as 30 days of vacation)
  
   
• you can develop your potential to the fullest (through a comprehensive virtual training program)
• your achievements are valued accordingly (e.g. through recognition and Senior-Leaders-Programs, as well as various company events)
• we think together with you about your future (e.g. through a company pension scheme

Research & Development

Senior Director, Head of Global Regulatory Medical Writing

Judith Horn, Human Resources

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.