Joulé
Clinical Research Physician / Principal Investigator - PT hours (Gastroenterolog
Joulé, Chattanooga, Tennessee, United States, 37450
Title: Clinical Research Physician / Principal Investigator - PT hours (Gastroenterology)
Please make an application promptly if you are a good match for this role due to high levels of interest.Location: Chattanooga, TN- onsite - Patient FacingType: Direct Hire, Part-timeSchedule: 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 experienced need, however it is a plus.
JOB DESCRIPTIONAs 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 clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborate with the team with all aspects of clinical and scientific input and safety evaluation.Essential Duties and Responsibilities: Provide clinical expertise into the conduct of clinical trialsBuild positive relationships and networks with internal and external medical professional and local opinion leadersWork closely with colleagues in other functions including, Regulatory Affairs, Clinical Operations and Patient EngagementLead and provide an oversight to a team of researchers and clinical staff involved in conduct of clinical trialsBe responsible for successful execution of research protocols according to FDA regulations and GCP guidelinesEvaluate study volunteer’s eligibility for clinical trialsPerform physical exams and assessments as required per research protocolsComplete all industry-required trainingAssess study patient health through interviews and physical examinationsCommunicate information to patients regarding diagnosis and treatment goalsReview all diagnostic reports and provide clinical direction to the study team
QUALIFICATIONSRequirements: 10 years' post training experience as a physician in gastroenterologyCurrently licensed to practice medicine in the state of hire with no history of license suspension or debarmentAdvanced knowledge of treatment and drug interactionsAbility to build rapport with patients and biopharmaceutical sponsorsStrong attention to detailStrong leadership qualitiesProvide clinical oversite to study teamClinical research experience
Please make an application promptly if you are a good match for this role due to high levels of interest.Location: Chattanooga, TN- onsite - Patient FacingType: Direct Hire, Part-timeSchedule: 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 experienced need, however it is a plus.
JOB DESCRIPTIONAs 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 clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborate with the team with all aspects of clinical and scientific input and safety evaluation.Essential Duties and Responsibilities: Provide clinical expertise into the conduct of clinical trialsBuild positive relationships and networks with internal and external medical professional and local opinion leadersWork closely with colleagues in other functions including, Regulatory Affairs, Clinical Operations and Patient EngagementLead and provide an oversight to a team of researchers and clinical staff involved in conduct of clinical trialsBe responsible for successful execution of research protocols according to FDA regulations and GCP guidelinesEvaluate study volunteer’s eligibility for clinical trialsPerform physical exams and assessments as required per research protocolsComplete all industry-required trainingAssess study patient health through interviews and physical examinationsCommunicate information to patients regarding diagnosis and treatment goalsReview all diagnostic reports and provide clinical direction to the study team
QUALIFICATIONSRequirements: 10 years' post training experience as a physician in gastroenterologyCurrently licensed to practice medicine in the state of hire with no history of license suspension or debarmentAdvanced knowledge of treatment and drug interactionsAbility to build rapport with patients and biopharmaceutical sponsorsStrong attention to detailStrong leadership qualitiesProvide clinical oversite to study teamClinical research experience