Clinical Research Physician - Internal Medicine

Benefits

Job Description

Qualifications

• •MD or DO degree
• •Active physician license (in good standing) in the state of practice for this role
• •Board certification in area of specialty required
• •CPR required
• •Clinical skills and clinical procedures based on area of specialty
• •Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm)
• •Strong organizational skills, attention to detail, and math proficiency
• •Well-developed written and verbal communication skills
• •Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers
• •Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities

Benefits

• •Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire
• •Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered
• •Shift & Schedule
• •Part time - 16-24 hrs/week

Responsibilities

• •This role involves conducting and coordinating daily clinical trial activities as a Principal Investigator, ensuring medical well-being and safety of study participants
• •The physician will drive clinical oversight and quality for assigned studies, adhering to ICH/FDA/GCP guidelines, study protocols, and company policies
• •Strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine
• •Local and central team collaboration
• •Ensure medical well-being and safety of study participants through ethical execution of clinical trials, adhering to FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, and company policies
• •Provide overall site leadership with a focus on enhancing efficiencies, patient safety, and protocol/GCP/regulatory compliance
• •Evaluate and assess participants to ensure only eligible individuals enroll in trials
• •Participate and engage in successful delivery and retention of study participants
• •Interact positively and collaboratively with sponsors, clients, and team members
• •Practice attention to detail in recording data and participant information, following protocol guidelines and GCPs
• •Actively involve in protocol training for staff
• •Participate in Investigator Meetings (IMs) and continuing education activities to maintain current knowledge of recruitment affairs and issues