Biotechnology Program Director
4 weeks ago
Albion Rye Associates is seeking a highly skilled and motivated Program Director to oversee and lead our multidisciplinary research and development programs in biotechnology.
Key Responsibilities:- Program Leadership: Lead the strategic planning, execution, and management of complex biotechnology programs from inception through to commercialization, ensuring alignment with the company's goals.
- Project Oversight: Oversee the progress of multiple R&D projects, ensuring key milestones, timelines, and deliverables are met within scope, budget, and regulatory compliance.
- Cross-Functional Collaboration: Work closely with scientific, technical, clinical, regulatory, and business development teams to ensure seamless coordination and integration of efforts across departments.
- Stakeholder Management: Serve as the primary point of contact for internal and external stakeholders, including partners, investors, and regulatory bodies, ensuring transparent and effective communication.
- Budget and Resource Management: Manage program budgets, allocate resources effectively, and ensure financial objectives are met. Optimize program performance by identifying risks and implementing mitigation strategies.
- Regulatory Compliance: Ensure all projects are conducted in accordance with relevant regulatory guidelines and industry standards (e.g., FDA, EMA, MHRA), maintaining the highest standards of quality and safety.
- Innovation and Strategy: Identify emerging trends, technologies, and market opportunities in biotechnology. Drive innovation by continuously evaluating new approaches and adjusting program strategies accordingly.
- Team Leadership: Build, mentor, and lead a high-performing team of project managers and researchers. Foster a collaborative and innovative culture that encourages scientific excellence.
- Advanced degree (PhD preferred) in biotechnology, life sciences, biochemistry, or a related field.
- Minimum of 10 years of experience in biotechnology, pharmaceuticals, or life sciences, with at least 5 years in a program or project management role.
- Proven track record of successfully managing complex, multi-disciplinary projects from R&D through to commercialization.
- Strong understanding of drug development processes, clinical trials, regulatory approvals, and manufacturing practices.
- Excellent leadership, communication, and interpersonal skills, with a demonstrated ability to lead cross-functional teams.
- Exceptional problem-solving abilities, with a proactive and strategic mindset.
- Experience managing relationships with external partners, stakeholders, and regulatory agencies.
- PMP or equivalent project management certification is desirable but not required.
- Experience in working within a fast-paced, innovative environment, and a passion for advancing biotechnology solutions.
- Competitive salary and performance-based bonuses
- Comprehensive health and wellness benefits
- Opportunities for professional growth and development
- Collaborative and dynamic work environment
- Contributing to transformative innovations in biotechnology
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