Hourly Wage for Research Doctor Salary in the United States

HIGHLIGHTS Opportunity to continue or break into clinical research! Be responsible for the success of various trials, working directly with the Principal Investigator/Physician Work with a small team = bigger influence on day-to-day! THE COMPANY Our client is a local clinical research company near Uptown Chicago that specializes in General Medicine clinical trials. Their goal is to serve the community and they are dedicated to providing the utmost quality care for their patients. They are looking to bring on a Clinical Research Physician Assistant (Sub-Investigator) to their team! THE ROLE As a Clinical Research Physician Assistant (Sub-Investigator), you will play a key role in conducting clinical trials and ensuring their success by following Good Clinical Practices (GCPs) and the company's Standard Operating Procedures (SOPs). You will collaborate with the Principal Investigator, monitor study participants, and maintain accurate study documentation. This position requires strong org

THIS ROLE IS FULL-TIME We are seeking a qualified and motivated physician interested to work as a Clinical Research Principal Investigator and join our dynamic team. As a key member of our clinical research site network, the Principal Investigator will play a crucial role in leading and overseeing clinical trials, ensuring the highest standards of research conduct and ethical practices. Responsibilities: Serve as the principal investigator for clinical trials conducted within our site network. Design and develop research protocols, ensuring compliance with regulatory requirements and industry standards. Lead the screening of eligible participants for clinical trials. Collaborate with cross-functional teams, including research coordinators, data managers, and regulatory affairs, to ensure seamless trial execution. Conduct thorough and accurate assessments of study participants, adhering to protocol guidelines. Maintain up-to-date knowledge of relevant therapeutic areas and research meth

THIS ROLE CAN BE EITHER FULL OR PART TIME! We are seeking a qualified and motivated dermatologist interested to work as a Clinical Research Principal Investigator and join our dynamic team. As a key member of our clinical research site network, the Principal Investigator will play a crucial role in leading and overseeing clinical trials, ensuring the highest standards of research conduct and ethical practices. Responsibilities: Serve as the principal investigator for clinical trials conducted within our site network. Design and develop research protocols, ensuring compliance with regulatory requirements and industry standards. Lead the screening of eligible participants for clinical trials. Collaborate with cross-functional teams, including research coordinators, data managers, and regulatory affairs, to ensure seamless trial execution. Conduct thorough and accurate assessments of study participants, adhering to protocol guidelines. Maintain up-to-date knowledge of relevant therapeutic

THIS ROLE CAN BE EITHER FULL OR PART TIME! We are seeking a qualified and motivated neurologist interested to work as a Clinical Research Principal Investigator and join our dynamic team. As a key member of our clinical research site network, the Principal Investigator will play a crucial role in leading and overseeing clinical trials, ensuring the highest standards of research conduct and ethical practices. Responsibilities: Serve as the principal investigator for clinical trials conducted within our site network. Design and develop research protocols, ensuring compliance with regulatory requirements and industry standards. Lead the screening of eligible participants for clinical trials. Collaborate with cross-functional teams, including research coordinators, data managers, and regulatory affairs, to ensure seamless trial execution. Conduct thorough and accurate assessments of study participants, adhering to protocol guidelines. Maintain up-to-date knowledge of relevant therapeutic a

Job Summary: As a Principal Investigator at this Clinical site, you will be responsible for safety monitoring of the in house/post dose safety of study participants enrolled into clinical trials. Essential Duties and Responsibilities: • To provide in house coverage to monitor and treat potential emergency medical situations for clinical trials participants including hypertensive crisis and cardiac emergencies. • Assessment of clinical data and clinical status of participants • Administration and/ or supervision of emergency drugs • Performing or supervising emergency medical procedures according to ACLS and/or protocol guidelines • Performing Physical Exams as needed • Decision on transfer of participants to local Emergency Rooms • Documentation of all occurrences • Review, initial and date all safety related data in a timely manner to include laboratory studies, ECGs and all other safety data as dictated by the study protocol. • Notification of Principal Investigator and study team of

Job Summary: As a Principal Investigator at this Clinical site, you will be responsible for safety monitoring of the in house/post dose safety of study participants enrolled into clinical trials. Essential Duties and Responsibilities: To provide in house coverage to monitor and treat potential emergency medical situations for clinical trials participants including hypertensive crisis and cardiac emergencies. Assessment of clinical data and clinical status of participants Administration and/ or supervision of emergency drugs Performing or supervising emergency medical procedures according to ACLS and/or protocol guidelines Performing Physical Exams as needed Decision on transfer of participants to local Emergency Rooms Documentation of all occurrences Review, initial and date all safety related data in a timely manner to include laboratory studies, ECGs and all other safety data as dictated by the study protocol. Notification of Principal Investigator and study team of any emergency sit