Ophthalmology Clinical Trials Lead & Research Mentor

Johns Hopkins University

Baltimore (MD)

On-site

USD 120,000 - 180,000

Full time

5 days ago
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Job summary

Johns Hopkins University in Baltimore invites applications for an entry‑level Assistant Professor of Ophthalmology to devote 100% effort to clinical trials and be available by cell phone to field questions from trial participants. The ideal candidate has prior clinical research experience in retinal diseases and ocular oncology.

Responsibilities include trial design, start-up procedures, IRB submissions, adverse event reporting, source document design, data entry in iMetadata, supervising study

Qualifications

  • MD and MPH required; public health ophthalmology degree desirable.
  • First-year Assistant Professor, 100% clinical trial focus.
  • Experience in retinal diseases and ocular oncology preferred.

Responsibilities

  • Clinical trial design and protocol development.
  • Study start-up procedures and regulatory submissions.
  • IRB submissions and adverse event reporting.
  • Design of source documents for trials.
  • Data entry into iMetadata.
  • Supervising and training study coordinators and post-doctoral fellows.
  • Communicating with sponsors and CRO/CRAs.
  • Interacting with study monitors and overseeing monitoring visits.
  • Experience managing audits by the FDA and EMA.

Skills

Clinical trial design
IRB submissions
Adverse event reporting
Communication with sponsors
Study coordination supervision
Regulatory compliance
Data entry in iMetadata
Teaching & mentoring

Education

MD
MPH

Tools

iMetadata

Job description

Johns Hopkins University in Baltimore invites applications for an entry‑level Assistant Professor of Ophthalmology to devote 100% effort to clinical trials and be available by cell phone to field questions from trial participants. The ideal candidate has prior clinical research experience in retinal diseases and ocular oncology.

Responsibilities include trial design, start-up procedures, IRB submissions, adverse event reporting, source document design, data entry in iMetadata, supervising study

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