System One
Clinical Research Physician / Principal Investigator - PT hours (Gastroenterolog
System One, Chattanooga, Tennessee, United States, 37450
Title:
Clinical Research Physician / Principal Investigator - PT hours (Gastroenterology)
Location:
Chattanooga, TN- onsite - Patient Facing
Type:
Direct Hire, Part-time
Schedule:
Approximately 8hrs/week, flexible scheduling with no evening or weekends required
Must be a US Board Certified MD, licensed to practice medicine in Tennessee. No prior clinical trial experience needed, however it is a plus.
JOB DESCRIPTION
As a Clinical Research Physician, you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients, health authorities, colleagues, and biopharmaceutical companies. Your role will be focused on clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborating with the team on all aspects of clinical and scientific input and safety evaluation.
Essential Duties and Responsibilities:
Provide clinical expertise into the conduct of clinical trials
Build positive relationships and networks with internal and external medical professionals and local opinion leaders
Work closely with colleagues in other functions including Regulatory Affairs, Clinical Operations, and Patient Engagement
Lead and provide oversight to a team of researchers and clinical staff involved in the conduct of clinical trials
Be responsible for successful execution of research protocols according to FDA regulations and GCP guidelines
Evaluate study volunteers’ eligibility for clinical trials
Perform physical exams and assessments as required per research protocols
Complete all industry-required training
Assess study patient health through interviews and physical examinations
Communicate information to patients regarding diagnosis and treatment goals
Review all diagnostic reports and provide clinical direction to the study team
QUALIFICATIONS
Requirements:
10 years' post-training experience as a physician in gastroenterology
Currently licensed to practice medicine in the state of hire with no history of license suspension or debarment
Advanced knowledge of treatment and drug interactions
Ability to build rapport with patients and biopharmaceutical sponsors
Strong attention to detail
Strong leadership qualities
Provide clinical oversight to the study team
Clinical research experience
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Clinical Research Physician / Principal Investigator - PT hours (Gastroenterology)
Location:
Chattanooga, TN- onsite - Patient Facing
Type:
Direct Hire, Part-time
Schedule:
Approximately 8hrs/week, flexible scheduling with no evening or weekends required
Must be a US Board Certified MD, licensed to practice medicine in Tennessee. No prior clinical trial experience needed, however it is a plus.
JOB DESCRIPTION
As a Clinical Research Physician, you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients, health authorities, colleagues, and biopharmaceutical companies. Your role will be focused on clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborating with the team on all aspects of clinical and scientific input and safety evaluation.
Essential Duties and Responsibilities:
Provide clinical expertise into the conduct of clinical trials
Build positive relationships and networks with internal and external medical professionals and local opinion leaders
Work closely with colleagues in other functions including Regulatory Affairs, Clinical Operations, and Patient Engagement
Lead and provide oversight to a team of researchers and clinical staff involved in the conduct of clinical trials
Be responsible for successful execution of research protocols according to FDA regulations and GCP guidelines
Evaluate study volunteers’ eligibility for clinical trials
Perform physical exams and assessments as required per research protocols
Complete all industry-required training
Assess study patient health through interviews and physical examinations
Communicate information to patients regarding diagnosis and treatment goals
Review all diagnostic reports and provide clinical direction to the study team
QUALIFICATIONS
Requirements:
10 years' post-training experience as a physician in gastroenterology
Currently licensed to practice medicine in the state of hire with no history of license suspension or debarment
Advanced knowledge of treatment and drug interactions
Ability to build rapport with patients and biopharmaceutical sponsors
Strong attention to detail
Strong leadership qualities
Provide clinical oversight to the study team
Clinical research experience
#J-18808-Ljbffr