If you are currently employed at Jazz, please apply through the Internal Career site.

Jazz Pharmaceuticals stands as a leading global biopharmaceutical entity committed to innovating and enhancing the lives of patients and their families. Our mission is to pioneer transformative medicines for individuals battling serious conditions, often with few or no existing therapeutic alternatives. Our diverse portfolio features prominent therapies aimed at sleep disorders and epilepsy, alongside an expanding range of cancer treatment options. By adopting a patient-centric and science-driven ethos, we fuel groundbreaking research and development across our comprehensive pipeline in oncology and neuroscience. With our headquarters located in Dublin, Ireland, we have research and development facilities, production sites, and teams worldwide dedicated to patient care. For further information about our initiatives, please visit our website.

Company Overview

As an international biopharmaceutical leader, Jazz Pharmaceuticals is dedicated to enhancing patient lives by discovering, developing, and bringing to market impactful products that meet significant medical needs. We are continually broadening our commercial offerings and advancing our R&D pipeline in therapeutic areas where our expertise shines.

Our primary therapeutic focus lies in sleep and hematology/oncology—fields in which we possess deep insights into the patient journey and a collection of products aimed at addressing vital healthcare gaps.

We seek passionate and highly skilled professionals to join our team. If you are eager to contribute to a company with a steadfast commitment to patient well-being and fostering a vibrant workplace culture, we invite you to explore our career opportunities at Jazz Pharmaceuticals.

Position Summary

As a vital part of the rapidly expanding Hematology/Oncology Therapeutic Area team, the Director of Clinical Development will play a key role in leading clinical initiatives. The position entails providing clinical leadership for global development strategies and protocols designed to support both new and existing programs. Key responsibilities include medical monitoring, overseeing scientific initiatives, analyzing, and disseminating clinical trial data, engaging in regulatory interactions, as well as building and managing external partnerships. The Director will also represent clinical development efforts within cross-functional teams at Jazz.

Key Responsibilities

• Lead and provide medical guidance for clinical programs, including protocol development, ongoing clinical trials, study reports, and regulatory documentation.
• Work collaboratively with colleagues in clinical development, operations, biostatistics, regulatory affairs, pharmacovigilance, and early development to ensure high-quality execution of clinical trials.
• Act as the medical monitor for clinical trials focused on Hematology/Oncology products, making informed recommendations based on safety findings and collaborating effectively with CROs and study investigators regarding eligibility and safety concerns.
• Analyze and approve safety and efficacy data contained within clinical study reports and regulatory submissions, including IND and NDA applications.
• Contribute strategic insights regarding new product ideas, long-term plans, and life-cycle management opportunities.
• Engage with external experts for scientific feedback and to ensure alignment with current clinical practices and guidelines, reflecting industry advancements in global development strategies.
• Establish and maintain robust relationships with outside collaborators and clinical investigators across the US and EU/ROW to support the clinical development program.
• Serve as a clinical resource for queries from collaborators, investigators, consultants, and corporate contacts.

Qualifications and Requirements

• A minimum of 3 years of experience in academic or pharmaceutical settings.
• Proven expertise in global clinical development within the Hematology/Oncology domain.
• Exceptional oral and written communication capabilities.
• In-depth understanding of GCP, Drug Safety, MedDRA safety coding, and Pharmacovigilance procedures.
• Exhibit values-driven leadership demonstrated through interactions at all organizational levels.
• Proactive and efficient working style, complemented by innovative problem-solving abilities.
• Willingness to travel, with potential travel requirements of 30-40% for short periods.

Education and Licenses

• MD or equivalent degree is mandatory.
• Board eligibility/certification in Hematology and/or Medical Oncology is preferred.
• US licensure and/or clinical practice experience is advantageous.

Jazz Pharmaceuticals is an equal opportunity employer, and all qualified individuals will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

Important Information for US Candidates

Jazz Pharmaceuticals, Inc. is committed to fair and competitive compensation practices, providing total compensation packages that align with market standards. The complete salary range for this role is: $240,000.00 – $360,000.00. Compensation within this range will reflect individual qualifications, skills, relevant experience, and other significant factors, ensuring alignment with the candidate’s expertise and contributions relative to our established pay framework. Regular reviews of this salary range will occur.

At Jazz, the base salary is just one component of your comprehensive compensation package. The successful candidate may also qualify for an annual cash bonus or incentive compensation based on the role, in accordance with the Company’s Global Cash Bonus Plan or Incentive Compensation Plan, alongside potential discretionary equity grants as part of Jazz’s Long Term Equity Incentive Plan.

Eligible employees will have access to various benefits offerings, including medical, dental, and vision insurance, a 401k retirement savings plan, and flexible paid vacation. For further details on our benefits, please visit our website.