Clinical Research Physician - Charleston, SC - Internal Medicine

• Provides overall site leadership with a focus on clinical oversight, study performance, enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance.
• Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes.
• Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
• Participates and engages in successful delivery and retention of study participants.
• Collaborates with investigators on the study protocols and overall study performance.
• May collaborate with departments leaders in Business Development, Patient Recruitment, Community Outreach, Finance, Budgets and Contracts, and Quality to coordinate delivery expectations, meet expected study milestones (such as site activation targets, enrollment targets, etc.), and delivery of quality data to sponsors.
• Interacts positively and collaboratively with sponsors, clients and team members.
• Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
• Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
• Provides training to staff, as needed, on study protocols, assignments and responsibilities.
• Employs strategic thinking and problem-solving skills to propose and implement risk mitigations.
• Participates and presents in management and/or site meetings.
• Perform other duties as assigned, requested, or required based on the needs of the participants, protocols, the site, and/or company.