Teva Senior Director Clinical Development 

Israel, Center District, Netanya 

24537633

• Serve as a senior leader within the organization and a core member of the Global Program Team, driving strategic clinical development initiatives.
• Develop, oversee, and manage multiple Clinical Development Plans with a focus on long-term program success and alignment with corporate goals.
• Lead cross-functional clinical development expert teams, ensuring optimal integration of efforts across all departments.
• Provide clinical leadership and oversight for study design, initiation, resource planning, implementation, and completion of global clinical trials.
• Represent clinical development in high-level internal and external meetings, including Investigator Meetings, advisory boards, and regulatory authority discussions.
• Lead interactions with global regulatory authorities, providing clinical expertise and strategic direction to facilitate successful submissions.
• Drive matrix collaboration with functional areas such as medical affairs, health economics, regulatory, commercial, and supply chain teams to ensure cohesive program execution.
• Oversee the preparation and review of clinical documents, including Protocols, Clinical Study Reports, Investigator’s Brochures, and global regulatory filings.
• Foster and maintain strategic partnerships with key opinion leaders, external collaborators, and academic institutions to advance clinical development objectives.
• Serve as medical monitor, providing high-level medical oversight, including study design, data analysis, patient safety, and CRO engagement.
• Proactively identify and mitigate risks across clinical programs, ensuring quality and compliance with all regulatory requirements.
• Mentor and develop clinical development team members, promoting a culture of excellence, innovation, and accountability.

Education Required

• MD with board certification in psychiatry (preferred) or other relevant specialties.
• Advanced training or specialization in clinical research, drug development, or related fields is highly desirable.

Experience Required

• A minimum of 3 years of pharmaceutical/biotechnology industry experience in clinical development, with a proven track record of leading programs through all stages of development, including regulatory approvals.
• Extensive experience managing and mentoring cross-functional teams in a matrix environment, with demonstrated ability to drive alignment and deliver results.
• Expertise in psychiatry or a related therapeutic area, with deep knowledge of disease-specific clinical and regulatory landscapes.
• Strong strategic thinking and decision-making skills, with the ability to balance short-term needs with long-term goals.
• Experience in global clinical trials, regulatory interactions, and dossier preparation for INDs, NDAs, and BLAs.
• Advanced understanding of clinical trial design, data analysis, and risk management practices.

Skills Required

• Exceptional interpersonal, leadership, and communication skills with the ability to influence across all organizational levels.
• Strong analytical capabilities and problem-solving skills to address complex clinical development challenges.
• High proficiency in managing multiple, simultaneous projects with aggressive timelines in a dynamic environment.
• Fluent in English, with superior oral and written presentation skills for internal and external audiences.

Alongside the fulfilling work, the inclusive culture and great rewards, our employees are entitled to a holistic benefits package, which is aimed to provide services required to their, and their families`, physical, emotional and social wellbeing.

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