Director Clinical Development - Respiratory

Date: May 20, 2025

Location:

Haarlem, Netherlands, 2031GA

Company: Teva Pharmaceuticals

Job Id: 61883

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

Possible working locations: Haarlem (NL), Krakow (PL), Runcorn (UK), Bucharest (RO), Zagreb (HR)

Are you ready to shape the future of global clinical programs? As Director, Clinical Development, you will drive the development, execution, and management of cutting-edge clinical research across all phases, ensuring innovation and excellence at every stage.

Your Impact:
• Strategic Leadership: Oversee and guide study teams, leading cross-functional collaborations in a dynamic matrix environment.
• Autonomy & Influence: Take charge of key clinical research projects with full ownership of protocols, Investigator’s Brochures, clinical study reports, and regulatory submissions.
• Cross-Functional Excellence: Work closely with commercial, regulatory, pharmacovigilance, CMC, early clinical, and pre-clinical teams to shape and execute asset strategy.
• Regulatory & Industry Leadership: Play a pivotal role in steering INDs, NDAs, BLAs, and global regulatory filings, influencing the future of drug development.

Join us in driving meaningful advancements in clinical research. If you're a visionary leader eager to make a global impact, we want to hear from you.

How you’ll spend your day

As a core member of the Global Project Team, as the Director of Clinical Development you will lead and oversee critical aspects of the clinical development process, ensuring the successful advancement of products through various phases. This role demands deep expertise in clinical development, strategic oversight, and cross-functional leadership.

Key Responsibilities
• Strategic Leadership: Develop, manage, and refine multiple Clinical Development Plans, ensuring alignment with company objectives and regulatory requirements.
• Cross-Functional Oversight: Lead and guide the clinical development team, collaborating with Global Clinical Operations to drive study implementation, resource planning, and trial execution.
• Regulatory & Compliance Excellence: Ensure clinical trials adhere to ICH, GCP, country-specific regulations, and company SOPs while managing safety concerns with Global Drug Safety and Pharmacovigilance teams.
• Scientific & Medical Contribution: Represent the organization at investigator meetings, advisory boards, and scientific conferences, delivering impactful presentations.
• Operational Execution: Secure necessary human resources, oversee clinical drug supply logistics, and partner cross-functionally with key stakeholders including Regulatory Affairs, Toxicology, Biostatistics, and more.
• Regulatory Documentation & Submissions: Lead the preparation of critical regulatory documents (IND/NDA), with the capability to spearhead NDA submissions independently.
• Data Interpretation & Publication: Guide the interpretation of clinical results, ensuring high-quality reporting in collaboration with Medical Writing. Author and review abstracts, manuscripts, and presentations for scientific dissemination.

Your experience and qualifications

• Advanced Medical & Scientific Expertise: MD, DO, or equivalent education combined with relevant industry experience. Exceptional PhD, PharmD, and DVM candidates with a proven leadership track record will also be considered.
• Strategic Clinical Leadership: experience in pharmaceutical industry or clinical trial management, with demonstrated ability to lead teams and drive projects forward. MD/DO candidates with deep clinical trial knowledge will also be considered, even without prior industry experience.
• Therapeutic Expertise: Strong preference for Respiratory, Pulmonary, or Allergy therapeutic areas, with an ability to shape research strategies and drive advancements.
• Influential Communication & Decision-Making: Exceptional interpersonal, verbal, and written communication skills to effectively collaborate with global cross-functional teams and present strategic insights.
• Agility & High-Performance Leadership: Ability to thrive in a dynamic, fast-paced environment, managing multiple priorities under time-sensitive conditions while maintaining a clear vision for success.

Already Working @TEVA?

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’s Equal Employment Opportunity Commitment

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.

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