Clinical Research Physician

About This Role

This role involves conducting and coordinating clinical trial activities, ensuring the medical well-being and safety of study participants while adhering to regulatory guidelines and company policies. The Principal Investigator will drive clinical oversight and quality for assigned studies.

Responsibilities

• Ensure medical well-being and safety of study participants through safe performance and ethical execution of clinical trials
• Adhere 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 compliance
• Evaluate and assess participants to ensure only eligible individuals enroll in trials
• Participate in the 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 involved in protocol training for staff
• Participate in Investigator Meetings (IMs) and continuing education activities

Requirements

• MD or DO degree
• Active physician license (in good standing) in the state of practice for this role
• Minimum of 2 years of experience in a medical research environment or equivalent
• Board certification in area of specialty preferred
• CPR required
• Clinical skills including phlebotomy, vitals, ECGs/EKGs, IVs, etc.
• Proficiency with computer applications such as MS Office, electronic health records, and web applications
• 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
• 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
• Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic
• High degree of urgency, self-motivation, integrity and dependability
• Ability to work independently to identify problems and implement solutions
• Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines

Qualifications

• MD or DO degree
• 2+ years of experience in a medical research environment, or equivalent combination of education and experience

Nice to Have

• Board certification in area of specialty
• ACLS preferred
• Bi-lingual (English / Spanish) proficiency

Skills

* Required skills

Benefits

Certifications