Associate Medical Director – Ophthalmic Clinical Oversight Lead
• Location: Remote (Global)
• Employment Type: Full-time
• Duration: Full-time (ongoing)
• Compensation: $280,000–$380,000/year, based on experience
Job Summary
• Deliver medical leadership and clinical oversight for ophthalmic drug delivery devices and combination product programs. This position supports end-to-end clinical strategy, safety monitoring, trial design, and regulatory engagements from early development through lifecycle management.
Key Responsibilities
• Deliver medical guidance on clinical development plans, trial design, and endpoints
• Oversee safety monitoring, adverse event evaluation, and risk-benefit analysis
• Support regulatory submissions and agency meetings through clinical data interpretation
• Partner with clinical operations, regulatory, and engineering teams on protocols and medical monitoring
• Review and approve clinical documents, investigator brochures, and safety reports
• Provide input on post-market surveillance and lifecycle clinical activities
Qualifications
• MD degree with 8+ years in clinical development or medical affairs (device or pharma experience preferred)
• Strong background in clinical trial oversight, safety, and regulatory strategy
• Experience with combination products or drug delivery devices
• Excellent medical writing, communication, and cross-functional leadership skills
• Ability to interpret clinical data and provide strategic medical guidance
• Self-directed with proven ability to manage multiple priorities
What We Offer
• Competitive full-time compensation and benefits
• Flexible remote scheduling
• Strategic impact on innovative device and combination product programs
• Platform collaboration tools
How to Apply
• To apply, visit our career portal and complete the quick and straightforward application process: enter your details, upload your CV, add your LinkedIn (optional), answer a few qualifying questions.
• Apply Now
• (Or visit:
https://www.pharmasmarket.com/signup/talent
)
Apply tot his job
Apply To this Job
• Employment Type: Full-time
• Duration: Full-time (ongoing)
• Compensation: $280,000–$380,000/year, based on experience
Job Summary
• Deliver medical leadership and clinical oversight for ophthalmic drug delivery devices and combination product programs. This position supports end-to-end clinical strategy, safety monitoring, trial design, and regulatory engagements from early development through lifecycle management.
Key Responsibilities
• Deliver medical guidance on clinical development plans, trial design, and endpoints
• Oversee safety monitoring, adverse event evaluation, and risk-benefit analysis
• Support regulatory submissions and agency meetings through clinical data interpretation
• Partner with clinical operations, regulatory, and engineering teams on protocols and medical monitoring
• Review and approve clinical documents, investigator brochures, and safety reports
• Provide input on post-market surveillance and lifecycle clinical activities
Qualifications
• MD degree with 8+ years in clinical development or medical affairs (device or pharma experience preferred)
• Strong background in clinical trial oversight, safety, and regulatory strategy
• Experience with combination products or drug delivery devices
• Excellent medical writing, communication, and cross-functional leadership skills
• Ability to interpret clinical data and provide strategic medical guidance
• Self-directed with proven ability to manage multiple priorities
What We Offer
• Competitive full-time compensation and benefits
• Flexible remote scheduling
• Strategic impact on innovative device and combination product programs
• Platform collaboration tools
How to Apply
• To apply, visit our career portal and complete the quick and straightforward application process: enter your details, upload your CV, add your LinkedIn (optional), answer a few qualifying questions.
• Apply Now
• (Or visit:
https://www.pharmasmarket.com/signup/talent
)
Apply tot his job
Apply To this Job