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Director Clinical Development - Respiratory

0-2 years
Not Disclosed
1 June 4, 2025
Job Description
Job Type: Full Time Education: PhD, PharmD, or DVM Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Director, Clinical Development – Respiratory

Date: May 20, 2025
Location: Haarlem, Netherlands, 2031GA (Other possible locations: Krakow, Runcorn, Bucharest, Zagreb)
Company: Teva Pharmaceuticals
Job ID: 61883


Who We Are

Teva Pharmaceuticals is committed to making good health more affordable and accessible. Operating in nearly 60 countries, we are the world’s leading manufacturer of generic medicines and a key producer on the WHO’s Essential Medicines List. Every day, over 200 million people take our medicines. We're seeking forward-thinkers who want to make a global impact in healthcare.


The Opportunity

We’re looking for a Director, Clinical Development – Respiratory to lead global clinical research programs across all development phases. You’ll be instrumental in strategic leadership, regulatory submissions, cross-functional alignment, and operational excellence in respiratory drug development.


Your Impact

Strategic Leadership & Oversight

  • Develop and manage multiple Clinical Development Plans in alignment with regulatory and business goals

  • Lead study teams and cross-functional collaborations within a matrixed global environment

  • Drive asset strategy and clinical execution in partnership with global stakeholders

Regulatory & Scientific Excellence

  • Oversee the creation of INDs, NDAs, BLAs, and other global regulatory filings

  • Represent Teva at investigator meetings, advisory boards, and scientific conferences

  • Ensure compliance with ICH-GCP, country-specific regulations, and internal SOPs

Operational Execution & Collaboration

  • Coordinate with functions like Regulatory Affairs, Clinical Operations, Biostatistics, Drug Safety, CMC, and more

  • Secure resources and manage clinical drug supply logistics

  • Lead interpretation and communication of clinical trial data

  • Author and review regulatory documentation, abstracts, and scientific publications


Your Experience and Qualifications

Education & Background

  • MD, DO preferred; PhD, PharmD, or DVM with extensive leadership experience in clinical development considered

  • Strong experience in clinical trial management and cross-functional team leadership

Clinical & Therapeutic Expertise

  • Preferred therapeutic experience in Respiratory, Pulmonary, or Allergy areas

  • Demonstrated ability to drive clinical research strategy and execution

Communication & Decision-Making Skills

  • Excellent interpersonal, verbal, and written communication skills

  • Ability to lead through influence and manage priorities under pressure in a fast-paced environment


Already Working @Teva?

If you're a current Teva employee, apply through the internal career site, Employee Central, for priority consideration and access to exclusive roles. For issues with EC access, contact your local HR/IT partner.


Equal Employment Opportunity Commitment

Teva Pharmaceuticals provides equal employment opportunity to all employees and applicants without regard to legally protected characteristics. We embrace diversity and aim to create an inclusive environment. If accommodations are needed during recruitment, they will be kept confidential and used only to support an accessible candidate experience.


Important Notice to Employment Agencies

Unsolicited CVs/resumes sent without a valid written agreement will become the property of Teva. No fee will be paid for any candidate hired under such circumstances.