Clinical Trials Research Assistant Professor Faculty Position at the Wilmer Eye Institute

Johns Hopkins University • Baltimore, MD

8h • Onsite

About The Position

The candidate will be entering their first year as an Assistant Professor and will devote 100% of their effort to clinical trials. This role requires availability by cell phone to answer questions from clinical trial participants. The position involves extensive experience in clinical research within retinal diseases and ocular oncology, encompassing all aspects of clinical trial management from design to regulatory compliance and team supervision.

Requirements

• Entering the first year as an Assistant Professor.
• Prior experience in clinical research in retinal diseases and ocular oncology.
• Knowledgeable and experienced in clinical trial design.
• Knowledgeable and experienced in study start-up procedures.
• Knowledgeable and experienced in IRB submissions.
• Knowledgeable and experienced in adverse event reporting.
• Knowledgeable and experienced in design of source documents.
• Knowledgeable and experienced in data entry into iMetadata.
• Knowledgeable and experienced in supervising and training study coordinators and post-doctoral fellows.
• Knowledgeable and experienced in communicating with sponsors and CRO/CRAs.
• Knowledgeable and experienced in interacting with study monitors and overseeing monitoring visits.
• Experience managing audits by the FDA and EMA.
• MD degree.
• MPH degree.

Nice To Haves

• A degree in public health ophthalmology is desirable in addition to an MPH.

Responsibilities

• Devote 100% effort to clinical trials.
• Be available by cell phone to field questions from clinical trial participants.
• Conduct clinical research in retinal diseases and ocular oncology.
• Manage clinical trial design.
• Oversee study start-up procedures.
• Handle IRB submissions.
• Manage adverse event reporting.
• Design source documents.
• Perform data entry into iMetadata.
• Supervise and train study coordinators and post-doctoral fellows.
• Communicate with sponsors and CRO/CRAs.
• Interact with study monitors and oversee monitoring visits.
• Manage audits by the FDA and EMA.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level