New Jersey Licensed Study Physician

Job Summary

A company is looking for a Study Responsible Physician (SRP).

Key Responsibilities

• Contribute to the design and development of clinical trial protocols and related documents
• Review and approve protocol-specific deviation criteria and manage safety reporting
• Provide training to study monitors and assist in site feasibility assessments

Required Qualifications

• 3+ years of industry experience in a relevant field
• Knowledge of guidelines and SOPs for clinical trials preferred
• Therapeutic domain experience in Ophthalmology preferred but not required
• Computer literacy
• Ability to work effectively in a team environment