Job Information
Teva Pharmaceuticals Senior Director, Disease Area Head in West Chester, Pennsylvania
Senior Director, Disease Area Head
Date: May 29, 2024
Location:
West Chester, United States, Pennsylvania, 19380
Company: Teva Pharmaceuticals
Job Id: 56160
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
As the Disease Area Head, you will play a pivotal role in shaping the product development strategy for immunology or neuroscience assets. Your responsibilities will span across clinical trial design, execution, and interpretation, ensuring the overall safety and efficacy of these products. You will collaborate with cross-functional teams, provide scientific leadership, and contribute to regulatory documents.
The Disease Area Head, Clinical Development is a critical leadership role, leading a team of physicians and scientists and responsible for providing the medical input and medical oversight within a therapeutic area(s). This may involve managing multiple assets or indications. Key strategic responsibilities include designing and executing clinical development plans for disease area across all stages of development. The incumbent will be responsible for leading clinical trials, developing and authoring/contributing to the essential documents (e.g. NDA/CTA submissions, study protocols, Investigator Brochures, regulatory briefing books and regulatory response documents, clinical study reports, etc.), reviewing study data and providing expert clinical insight.
The Disease Area Head will play a key role in cross-functional study teams, offering effective feedback and strategic insights. This position provides medical leadership within their field of expertise, contributing to Teva’s clinical development programs. Additionally, the role involves senior stakeholder management, regulatory interactions, and input at a broader R&D level, including business development opportunities. The disease area head will also work closely with the VP Cross TA lead to ensure alignment on clinical development strategy decisions and advancing clinical development objectives related to the specific disease area.
How you’ll spend your day
Directing and implementing clinical research plans and programs according to established design principles
Direct management of a team of physicians and clinical leads. Provide leadership guidance, responsible for the team members individual development, training, ensuring appropriate resource allocation, etc.
Drive the integration of clinical development strategies across the therapeutic area
Leading the development of Clinical Protocols to meet CDP objectives
Overseeing Study Director(s) and drive the execution of the study from protocol concept to final report including interpretation of clinical data
Overseeing the Medical Monitor(s) for a study or clinical program, reviewing and monitoring study safety data
Implementing strategies to identify, monitor and resolve clinical/program trial issues
Serving as the clinical/medical team expert to provide direction to all program team functions
Organizes Advisory Board meetings (e.g., agenda setting), and identifying and liaising with KOLs regarding program strategy and scientific advice
Interpreting study data and developing integrated summaries for safety and efficacy.
Contributing clinical expertise and content to regulatory documents (e.g. briefing books, NDAs, etc.)
Represent Clinical teams in discussions with Health Authorities
Setting key deadlines and project milestones within function
Reviewing 3rd party (contractors, consultants and vendors) work product and deliverables to approve payment of invoices and resolves issues
Your experience and qualifications
MD is required
In depth knowledge of the disease area. Expertise in late-stage clinical trials. At least 5 years of relevant biopharmaceutical industry clinical development experience in immunology clinical research
Solid knowledge and experience of overall and early clinical development
In depth knowledge of the disease area, gastrointestinal is preferred
Clinical experience and academic track record in a specific disease area is highly desirable. Completion of a disease area fellowship is also preferred
Demonstrated competence and track record at Study Director/ Clinical Lead level
Experience with FDA or EMA regulatory agencies handling responses to inquiries and requests for study related information desired
Candidates should have experience and understanding of running clinical studies with substantial interaction with other Clinical Development functions such as Clinical Operations, Regulatory and Data Management and Program Leadership
The ability to be a self-starter, self motivated and effective in influencing others
The ability to provide guidance to Medical Monitors/ Clinical Scientists reporting into the Senior Vice President, Global Late Clinical Development
Board certification or eligibility in the relevant disease area preferred
Advanced knowledge and clinical training in medical/scientific areas
Well-developed leadership skills with the ability to influence, able to make decisions and defend them. This individual will be highly visible at different levels of the organization and must be able to build trust and credibility.
Ability to push innovation and creative thinking. Strategic thinking, accountable and forward-looking; able to see a larger business picture.
Flexible, able to wear many hats, work in a fast-paced environment and be open to change or the unknown
Excellent interpersonal, presentation and communication skills, highly collaborative
Ability to interface professionally with a wide spectrum of internal and external academicians, agencies, and industry executives in the scientific/medical arena
Hard working, energetic and passionate about making a difference
Highest integrity, committed to ethics and scientific standards
Taking initiative, thinking “on the fly”; hands-on, decisive and being self assured are critical
Ability to work in a dynamic and global company
Enjoy a more rewarding choice
We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance.
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 (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)
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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EOE including disability/veteran