Director, Clinical Development – Respiratory
Date Posted: May 28, 2025
Location: Parsippany, NJ, United States, 07054 (Hybrid with flexibility; West Chester, PA option available)
Company: Teva Pharmaceuticals
Job ID: 59023
Who We Are
At Teva, we’re committed to improving health worldwide by making it more affordable and accessible. As the global leader in generic medicines, we serve 200 million people daily. We operate in nearly 60 countries, offering diverse talent the opportunity to contribute to something impactful. We're seeking visionary professionals eager to make a difference in global health.
The Opportunity
We are looking for a Director, Clinical Development – Respiratory to lead global clinical programs across all phases of research. This individual will have cross-functional leadership responsibilities and serve as a core clinical leader for respiratory, pulmonary, and atopic disease area assets.
How You’ll Spend Your Day
Strategic & Clinical Development Leadership
Lead global clinical development efforts for respiratory/pulmonary assets.
Develop and manage multiple Clinical Development Plans (CDPs).
Serve as a core member of the Global Project Team.
Guide cross-functional teams through matrixed leadership.
Interface with Commercial, Regulatory, Pharmacovigilance, CMC, and Preclinical teams to align on asset strategy.
Operational & Scientific Oversight
Oversee protocol development, investigator brochures, study reports, and regulatory submissions (INDs, NDAs, BLAs).
Collaborate with Global Clinical Operations for trial implementation, timelines, and resourcing.
Ensure compliance with ICH, GCP, Teva SOPs, and local regulations.
Support regulatory agency interactions and presentations.
Analyze clinical trial data, guide reporting and publication efforts.
Scientific Representation & External Engagement
Represent Teva at investigator meetings, advisory boards, and scientific conferences.
Foster external KOL relationships and represent the company with regulatory authorities.
Your Experience and Qualifications
Education & Experience
MD/DO required; exceptional PhD, PharmD, or DVM candidates with strong clinical trial leadership may be considered.
Minimum 2 years of industry experience (clinical trial management, pharma/biotech), or relevant clinical trial experience in academic or medical settings for MD/DOs.
Therapeutic area expertise in Respiratory, Pulmonary, or Allergy is strongly preferred.
Skills & Traits
Strong interpersonal, verbal, and written communication skills.
Strategic, organized, and effective at managing concurrent priorities.
Ability to work in fast-paced, high-impact, and cross-functional environments.
Travel
Approximately 30% domestic and international travel required.
Benefits Overview
Health Coverage: Medical, Dental, Vision, Rx — starting Day 1
Retirement: 401(k) with up to 6% match, plus 3.75% annual company contribution
Time Off: Generous PTO, 13 paid holidays, 3 floating holidays
Additional Perks: Parental leave, employee stock purchase plan, tuition reimbursement, lifestyle & wellness programs, identity theft protection, and more
Work Location
Hybrid model preferred in Parsippany, NJ or West Chester, PA (3 days onsite per week). Remote arrangements may be considered for highly qualified candidates.
Already Working @Teva?
Apply through the Internal Career Site on Employee Central for priority consideration and access to internal-only roles. Contact your HR or IT partner if access issues occur.
Equal Employment Opportunity Commitment
Teva is committed to equal opportunity and inclusivity in the workplace. We welcome applications from individuals regardless of age, race, religion, gender, sexual orientation, disability, veteran status, or other protected status.
Important Notice to Agencies
Unsolicited resumes from recruiters without a signed agreement will be considered property of Teva, and no fees will be paid.
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