Senior Director, Drug Development at Jobgether

, , United States -

Full Time

Start Date

Immediate

Expiry Date

03 Oct, 26

Salary

0.0

Posted On

05 Jul, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Drug Development Strategy, Clinical Development Plans, Regulatory Affairs, Portfolio Management, Due Diligence, Risk Assessment, Cross-functional Leadership, Target Product Profiles, Study Design, Regulatory Submissions, Strategic Thinking, Stakeholder Management, Microsoft Excel, Microsoft PowerPoint, Scientific Rigor, Analytical Problem Solving

Industry

Internet Marketplace Platforms

Description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Director, Drug Development based in the United States. This senior leadership role sits at the core of global pharmaceutical and biotech innovation, driving end-to-end drug development strategy across multiple therapeutic areas. You will shape integrated clinical, regulatory, and commercial development plans that guide assets from early discovery through approval and market launch. The role combines scientific depth with strategic advisory influence, supporting high-impact decisions such as go/no-go evaluations, licensing opportunities, and portfolio prioritization. You will engage directly with regulatory agencies and key industry stakeholders, contributing to submissions and high-level scientific discussions. This position also plays a visible external role, representing thought leadership through conferences, publications, and strategic client engagements. Working in a highly collaborative, global environment, you will partner with cross-functional teams to accelerate innovation and improve development success rates. The role offers the opportunity to directly influence the advancement of therapies that can meaningfully improve patient outcomes worldwide. \n Accountabilities: Lead the development of integrated drug development strategies spanning preclinical, clinical, regulatory, and commercial dimensions for pharmaceutical and biotech programs. Provide expert guidance on clinical development plans, target product profiles, study designs, and regulatory submission strategies (e.g., INDs, NDAs, BLAs, MAAs). Conduct regulatory and development risk assessments, including probability of success analyses, gap assessments, and mitigation strategy design. Support and participate in interactions with global regulatory authorities (FDA, EMA, and others), including preparation of briefing materials and attendance at meetings. Advise on portfolio management decisions, licensing opportunities, and strategic investment evaluations across development programs. Contribute to due diligence activities and strategic business development initiatives, including client presentations and partnership discussions. Provide leadership within cross-functional drug development teams, ensuring alignment across scientific, clinical, and commercial stakeholders. Requirements: Master’s degree or higher in life sciences, medicine, pharmacy, or a related field, or equivalent professional experience. 15–20+ years of experience in clinical research and drug development with global or multi-regional exposure. Proven track record in senior strategic roles within pharmaceutical or biotech drug development environments. Strong expertise across clinical development strategy, regulatory affairs, and lifecycle product development. Deep understanding of regulatory processes and global health authority interactions (FDA, EMA, and similar agencies). Experience developing clinical development plans, protocols, and regulatory submission documents. Strong analytical, strategic thinking, and problem-solving capabilities with a data-driven mindset. Excellent communication and presentation skills, with the ability to influence senior stakeholders and clients. Demonstrated leadership ability managing cross-functional teams and complex development programs. High level of proficiency in Microsoft Excel and PowerPoint. Strong commitment to scientific rigor, quality, and ethical standards in drug development. Benefits: Competitive base salary with significant performance-based compensation potential Annual salary range reflective of experience, expertise, and location Bonus and incentive programs tied to individual and organizational performance Comprehensive health coverage including medical, dental, vision, and wellness benefits Retirement savings plan with employer contributions Flexible remote/hybrid work arrangements depending on role requirements Paid time off, holidays, and additional leave options Access to professional development, learning programs, and global scientific engagement opportunities Opportunities to participate in conferences, publications, and industry thought leadership initiatives Inclusive, global work environment focused on innovation and patient impact. \n How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1

Responsibilities

Lead end-to-end drug development strategies across preclinical, clinical, regulatory, and commercial dimensions for pharmaceutical and biotech programs. Provide strategic guidance on portfolio management, regulatory submissions, and interactions with global health authorities like the FDA and EMA.