Board Certified Ophthalmologist – Senior Medical Director

This is a fully remote position, open to applicants in Arizona, +4 more states.

📋 Description

• Oversees medical aspects of designated clinical studies while acting as a medical monitor.

• Frequently acts as the main medical point of contact for clients regarding assigned clinical studies.

• Offers medical insights and supervision in collaboration with the Drug Safety and Pharmacovigilance department.

• Responsible for the design and development of study protocols, as needed.

• Contributes to modifications of study protocols.

• Creates and facilitates project-specific and therapeutic training for project team members and clinical site personnel.

• Supplies medical and therapeutic insights for Study Start Up, Feasibility, and Subject Identification initiatives.

• Provides medical input for data collection instruments, monitoring strategies, and review and analysis frameworks.

• Supervises assigned Medical Scientist staff and collaborates with Medical Director colleagues to evaluate clinical data.

• Offers medical coverage outside of regular hours for clinical studies.

⛳️ Requirements

• Board certification in Ophthalmology is mandatory.

• Oversees medical aspects of designated clinical studies while acting as a medical monitor. Frequently serves as the primary medical contact for clients regarding assigned clinical studies.

• Provides medical insights and oversight in collaboration with the Drug Safety and Pharmacovigilance department.

• Responsible for the design and development of study protocols, as needed. Contributes to modifications of study protocols.

• Creates and facilitates project-specific and therapeutic training for project team members and clinical site personnel; provides training to client staff as necessary.

• Supplies medical and therapeutic insights for Study Start Up, Feasibility, and Subject Identification initiatives, which includes reviewing Informed Consent Templates and Subject-Facing Materials, along with input for site feasibility assessments.

• Provides medical input for data collection instruments, monitoring strategies, and review and analysis frameworks.

• Supervises assigned Medical Scientist staff and collaborates with Medical Director colleagues to evaluate clinical data. Presents identified trends and issues, along with mitigation strategies, to clients and project team members to reduce risks to subject safety and the integrity of study data.

• Offers medical coverage outside of regular hours for clinical studies.

• Complies with all enterprise policies, work instructions, standard operating procedures, and project plans. Follows client policies and standard operating procedures as required in project plans.

• Maintains comprehensive knowledge of FDA and global drug development regulations and national and ICH Good Clinical Practice (GCP) guidelines.

• May assist with responses to Requests for Proposals (RFPs) or Bid Defense Meetings (BDMs), as requested.

• May contribute insights to clinical development or regulatory teams within the Company, as requested.

• May represent the Company at scientific conferences, upon request.

🏝️ Benefits

• Health benefits including Medical, Dental, and Vision coverage.

• Company-matched 401k plan.

• Eligibility to participate in the Employee Stock Purchase Plan.

• Opportunity to earn commissions or bonuses based on company and individual performance.

• Flexible paid time off (PTO) and sick leave.