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    Director Clinical Development - Oncology

    Teva Pharmaceuticals
    2-4 years
    Not Disclosed
    Parsippany
    10 Nov. 21, 2024
    Job Description
    Job Type: Full Time Education: MD/DO/PhD/Pharm.D/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

    Who We Are

    At Teva Pharmaceuticals, we are on a mission to make good health more affordable and accessible, enabling millions worldwide to enjoy healthier lives. This mission unites our global team spanning nearly 60 countries, representing a rich diversity of nationalities and backgrounds.

    As the world’s leading manufacturer of generic medicines and a proud producer of many products on the World Health Organization’s Essential Medicines List, we impact the lives of at least 200 million people every day. While this is an extraordinary achievement, we continuously seek innovative ways to expand our reach and welcome new talent to join us in making a difference.

    Position: Director, Clinical Programs

    Location: West Chester, PA, or Parsippany, NJ (Hybrid Work Environment)
    Travel Requirements: ~30% (Domestic and International)

    Role Overview

    The Director, Clinical Programs will lead the development, execution, and management of multiple clinical programs worldwide across all phases of clinical research. This role involves working in a matrix environment to oversee study teams, prepare and review key documents, and provide clinical leadership for assigned asset strategies.

    The Director will play a critical role in the clinical development and regulatory submission process, collaborating closely with cross-functional teams such as commercial, regulatory, pharmacovigilance, CMC, and pre-clinical development.

    Key Responsibilities

    Leadership & Strategy

    • Develop and manage Clinical Development Plans for multiple programs.
    • Provide clinical leadership for INDs, NDAs, BLAs, and other regulatory filings.
    • Act as a core member of the Global Project Team and contribute to asset strategy development.
    • Foster relationships with key opinion leaders (KOLs) in the Oncology therapeutic area.

    Operational Oversight

    • Lead or oversee cross-functional clinical development teams.
    • Support Global Clinical Operations in trial initiation, resource planning, and study execution.
    • Work with the Clinical Supplies Group to ensure timely procurement of clinical drug supplies.
    • Resolve clinical and safety issues in collaboration with Global Drug Safety and Pharmacovigilance.

    Document Preparation & Communication

    • Prepare and review key clinical documents, including protocols, Investigator’s Brochures, clinical study reports, and regulatory submission summaries.
    • Represent Teva at scientific meetings, advisory boards, and regulatory agency meetings as needed.
    • Author and review abstracts, posters, and manuscripts, and present data at scientific events.

    Collaboration & Cross-Functional Integration

    • Partner with departments such as Regulatory Affairs, CMC, Toxicology, Biostatistics, and Marketing to execute Clinical Development Plans.
    • Analyze and interpret clinical trial results in collaboration with Medical Writing teams to prepare high-quality reports.

    Qualifications

    Education

    • MD, DO, or equivalent.
    • PhD, PharmD, or DVM with a proven track record in clinical development will be considered.

    Experience

    • Minimum 3 years of experience in pharmaceutical clinical trial planning and management.
    • Proven ability to manage projects and lead cross-functional teams effectively.
    • Oncology therapeutic area experience is strongly preferred.
    • Relevant clinical trial knowledge for MD/DO candidates without prior industry experience will be considered.

    Skills

    • Excellent interpersonal, verbal, and written communication skills.
    • Strong project management and multitasking abilities.
    • Ability to work independently in a fast-paced, deadline-driven environment.

    What We Offer

    Teva provides a comprehensive benefits package, including:

    • Health Coverage: Medical, Dental, Vision, and Prescription coverage starting Day 1.
    • Financial Benefits: 6% 401(k) match, Employee Stock Purchase Plan, and Tuition Assistance.
    • Paid Time Off: Generous PTO, 13 paid holidays, and more.
    • Additional Perks: Disability and Life Insurance.

    Equal Employment Opportunity Commitment

    Teva Pharmaceuticals is committed to creating a diverse and inclusive workplace. We provide equal employment opportunities regardless of age, race, gender, disability, or any other legally protected status.

    If you require accommodations during the recruitment process, please let us know. Your information will remain confidential and used solely to ensure an accessible experience.

    Application Process

    Internal Candidates
    Teva employees should apply through the internal career site, "Employee Central," for priority consideration.

    External Candidates
    Submit your application through Teva’s external career portal.

    Agency Policy
    Teva does not accept unsolicited resumes from recruitment agencies. Resumes submitted without a valid agreement will become Teva’s property, and no fees will be paid.

    Join us in advancing global health and making a meaningful difference in millions of lives!

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