Director Clinical Development - Oncology

3+ years

Not Disclosed

Parsippany

10 Jan. 3, 2025

Job Description

Job Type: Full Time Education: MD/DO 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 - Oncology
Location: Parsippany, NJ, USA (Hybrid)
Date Posted: December 9, 2024

Join Teva Pharmaceuticals, a global leader in making healthcare more accessible and affordable. With a presence in nearly 60 countries, Teva develops innovative medicines to improve the lives of millions worldwide.

The Opportunity

The Director of Clinical Development - Oncology will lead clinical programs across all phases of research, ensuring compliance with global standards and regulations. This individual will work collaboratively in a matrixed environment, developing strategies, overseeing study teams, and ensuring successful execution of clinical trials.

Key Responsibilities

Strategic & Operational Leadership:
- Serve as a core member of the Global Project Team.
- Lead cross-functional clinical development teams and oversee multiple Clinical Development Plans.
- Partner with key departments (Regulatory, Biostatistics, Marketing, etc.) to execute Clinical Development Plans.
Clinical & Regulatory Oversight:
- Ensure clinical trials comply with ICH, GCP, and relevant country laws.
- Manage the preparation of key documents, including protocols, Investigator’s Brochures, and regulatory submissions.
- Represent Teva at advisory boards, KOL meetings, and scientific/regulatory forums.
Stakeholder Engagement:
- Build and foster relationships with opinion leaders in oncology.
- Present at investigator meetings and collaborate with Clinical Supplies Group for procurement and drug supply planning.
Documentation & Communication:
- Author and review abstracts, posters, and manuscripts.
- Analyze and interpret clinical data to prepare high-quality reports in collaboration with Medical Writing.

Your Qualifications

Education:
- MD, DO, or equivalent; PhD, PharmD, or DVM with a proven track record may also be considered.
Experience:
- Minimum of 3 years in the pharmaceutical industry or related field, with oncology expertise strongly preferred.
- Proven ability to manage clinical trials and lead project teams.
- Managerial experience (2-4 years) is a plus.
Skills:
- Strong interpersonal, verbal, and written communication skills.
- Ability to manage multiple priorities in a fast-paced environment.
- Willingness to travel domestically and internationally (~30%).

Work Environment

This hybrid role is based out of Parsippany, NJ or West Chester, PA, with on-site presence required several days a week.

Benefits

Health & Wellness:
- Comprehensive Medical, Dental, Vision, and Prescription coverage starting Day 1.
Financial Security:
- 401(k) with a 6% employer match and Employee Stock Purchase Plan.
Work-Life Balance:
- Paid Time Off, 13 paid holidays, and tuition assistance.
Additional Perks:
- Life and Disability Insurance, Employee Assistance Program, and more.

Equal Employment Opportunity

Teva Pharmaceuticals is committed to fostering an inclusive workplace and providing equal employment opportunities to all qualified individuals.

Application Process for Current Teva Employees
Employees are encouraged to apply through the internal Employee Central portal for priority consideration.

Notice to Employment Agencies
Teva does not accept unsolicited agency assistance for employment opportunities without prior written agreements.

Embark on a meaningful career with Teva today, shaping the future of oncology treatments and improving patient outcomes!

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Director Clinical Development - Oncology

Job Description

The Opportunity

Key Responsibilities

Your Qualifications

Work Environment

Benefits

Equal Employment Opportunity

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