Vice President of Research and Development (VP R&D) Pharma - Ophthalmic Drug Products

Job Title: Vice President of Research and Development (VP R&D) Pharma - Ophthalmic Drug Products

Immediate position, On-Site full-time position in Ramat Hahayal, Tel Aviv, Israel

ABLE Tx is seeking a VP R&D Pharma (Ophthalmic Drug Products)

ABLE is actively seeking an enthusiastic VP R&D Pharma to join our dynamic team developing novel ophthalmic drug products.

ABLE is focusing on effective ocular therapies. ABLE develops innovative pharmaceutical products designed for leading causes of visual impairment and blindness, to make a clinically significant difference in patients' lives.

The VP R&D Pharma, at our innovative pharmaceutical startup, will be at the forefront of an exciting new venture, gaining a distinctive and empowering experience in both learning and leadership.

The VP R&D will be responsible for overseeing the management, and execution of our R&D programs. This role requires a deep understanding of ocular pharmacology, extensive experience in pharmaceutical R&D, and a proven track record of leading cross-functional teams to successfully bring drug products from concept through clinical development to market.

Key Responsibilities:

1. Project Management:

  - Lead and manage all phases of the drug development process, including discovery, preclinical, clinical, and regulatory.

  - Ensure timely and cost-effective progression of projects from preclinical stages through clinical trials.

  - Oversee the development and implementation of project plans, including timelines, budgets, and resource allocation.

2. Team Leadership:

  - Build, mentor, and lead a high-performing R&D team, fostering a culture of innovation and excellence.

  - Facilitate collaboration between R&D, clinical development, regulatory affairs, and other departments.

  - Recruit top talent and manage team performance, development, and motivation.

3. Innovation and Collaboration:

  - Identify and evaluate new technologies, scientific advancements, and partnerships that can enhance the company’s R&D capabilities.

  - Establish and maintain relationships with key external stakeholders, including CRO’s, academic institutions, research organizations, and industry partners.

  - Represent the company at scientific conferences, industry meetings, and other relevant forums.

4. Regulatory and Compliance:

  - Ensure compliance with all regulatory requirements, including FDA, EMA, CE and other relevant authorities.

  - Oversee the preparation and submission of regulatory filings and responses to regulatory inquiries.

  - Monitor and address potential risks and challenges related to regulatory approval and product development.

5. Budget, Timeline and Resource Management:

  - Develop and manage the R&D budget & timeline ensuring efficient use of resources and alignment with company financial & timeline goals.

  - Monitor expenditures and performance metrics, making adjustments as necessary to meet project and business objectives.

Qualifications:

- Education: Advanced degree (PhD, MD, or equivalent) in a relevant scientific field such as pharmacology, biochemistry, or a related discipline.

- Experience: Minimum of 10-15 years of experience in pharmaceutical R&D, with at least 5 years in a senior leadership role. Well versed in EU and FDA regulations including GCP. Experienced in reading and summarizing scientific literatures. Experience specifically in ocular drug development is highly desirable.

- Expertise: Strong knowledge of ocular pharmacology, drug development processes, clinical trials, and regulatory requirements.

- Leadership: Proven ability to lead and inspire cross-functional teams, manage complex projects, and drive strategic initiatives.

- Skills: Excellent project management skills. Excellent communication, negotiation, and presentation skills. Strong problem-solving abilities and a strategic mindset.

- Additional Requirements: Demonstrated track record of successful drug development programs and experience with commercialization of ocular therapies is preferred.

- Must have excellent English.

- Must be able to travel in Israel and abroad with overnight stays, as necessary.

- This On-Site full-time position is in Ramat Hahayal, Tel Aviv, Israel.

Why Join Us:

At ABLE, you will be part of a forward-thinking team dedicated to improving the sight of patients with ocular conditions. We offer a dynamic work environment, competitive compensation, and opportunities for professional growth and development.

How to Apply:

Interested candidates should submit their resume and a cover letter outlining their qualifications and experience to office@able-tx.com. Please include "VP R&D Pharma Application" in the subject line.

Join us in shaping the future of Ophthalmology !