Senior Medical Director (Retina)

The Lotus Group LLC; United States; Remote; USD 180,000 - 240,000; Full time

Job summary

A leading biotechnology firm in the US is seeking a Senior Medical Director for remote strategic and clinical leadership in late-stage ophthalmology programs. The ideal candidate will possess an MD with board certification in ophthalmology, extensive biotech experience, and strong communication skills. This executive role offers a chance to shape clinical development strategies and engage with regulatory authorities while mentoring junior staff.

Qualifications

• 3+ years of industry experience within biotech or pharmaceutical clinical development.
• Demonstrated success in late-stage clinical development and regulatory submissions.
• Ability to thrive in a fast-paced biotech environment.

Responsibilities

• Serve as the medical lead for late-stage clinical development programs in ophthalmology.
• Provide clinical oversight for protocol design and data interpretation.
• Mentor and guide junior physicians and clinical development staff.

Skills

Clinical oversight

Regulatory interactions

Strong communication

Relationship building

Entrepreneurial mindset

Education

MD with Board Certification in Ophthalmology

Job description

Our client is a publicly traded biotechnology company advancing a diverse portfolio of late-stage ophthalmology programs. With a focus on delivering transformative therapies, they are committed to improving outcomes for patients living with serious eye diseases.

The Role

The Senior Medical Director will provide strategic and clinical leadership across late-stage ophthalmology programs. This individual will play a pivotal role in shaping clinical development strategy, collaborating cross-functionally, and engaging with regulatory authorities and key opinion leaders.

Key Responsibilities

• Serve as the medical lead for late-stage clinical development programs in ophthalmology.
• Provide clinical oversight for protocol design, execution, and data interpretation.
• Partner with regulatory affairs on submissions and interactions with global health authorities.
• Represent the company at medical and scientific meetings, establishing strong KOL and investigator relationships.
• Contribute to publication strategy and medical communications to support development programs.
• Provide clinical input to cross-functional teams including Clinical Operations, Biometrics, and Safety.
• Mentor and guide junior physicians and clinical development staff.

Qualifications

• MD with Board Certification in Ophthalmology required.
• 3+ years of industry experience within biotech or pharmaceutical clinical development.
• Demonstrated success in late-stage clinical development and regulatory submissions.
• Strong communication skills with the ability to effectively interact with internal and external stakeholders.
• Track record of building relationships with investigators, KOLs, and regulatory authorities.
• Entrepreneurial mindset and ability to thrive in a fast-paced biotech environment.

Location

This is a remote position within the United States.

Seniority level

Executive

Employment type

Full-time

Job function

Management and Research

The company is an equal opportunities employer and welcomes applications from diverse candidates.