Gastroenterology Physician Gastroenterologist (GI) – Physicians Only Apply – Perm Position Available In Pinellas, Florida

Job Description:

A Gastroenterology Physician Gastroenterologist (GI) practice isseeking a qualified physician for Saint Petersburg, FL. This andother physician jobs brought to you by ExactMD. Medical DoctorsOnly Apply. Company

• -We have been offering medical research to residents ofCentral Florida since 2000. With six privately-owned clinical trialfacilities our mission is to provide consistent, high-qualityclinical research in a professional, ethical and timely manner
• -Weare looking for a Principal Investigator who can contributeimmediately to our rapidly growing CNS and Neurology researchpractice
• Our company is driven by providing excellent care toour subjects and best in class research for our sponsors via adynamic team of physicians, raters, nurses, and administrativepersonnel. This is 100% outpatient opportunity working Monday thruFriday 9AM to 4pm or 8AM to 5pm
• –

Position Summary:

• -Seeking aGastroenterologist Physician that will serve as a Principal orSub-Investigator for clinical trials with pharmaceutical companiestesting new medications. The Principal Investigator is responsiblefor conducting clinical trials in accordance with the researchprotocol, Good Clinical Practices (GCPs), and federal/stateregulations
• The PI will collaborate with our study team, as wellas various medical, pharmaceutical company and regulatory personnelto ensure the health and welfare of study participants. Salary iscompetitive with full benefits, health, 401K, disability, andsigning bonus
• -Job Responsibilities
• -1•Maintain currentlicense to practice medicine.

2

• Assume responsibility as thePrincipal or Sub-Investigator for the duration of clinicaltrials.3
• Strong working knowledge of regulatoryrequirements and GCP standards.4
• Possess thoroughunderstanding of the clinical research protocol and patientpopulation for which the trial is designed.5
• Performevaluations.6
• Complete training as required persponsor
• -s vendors to obtain certification to conduct testing andrating scales for specific protocols.7
• Conducttesting and rating scales per sponsor
• -s instructions andprotocols
• Completion of all documentation, paper and electronic,as required per protocol.8
• Evaluate subjects for clinicalresearch trials based on their past medical and psychiatric historyin comparison to the protocol specific inclusion and exclusioncriteria.9
• Ensure appropriate delegation and training of theclinical research staff.10
• Educate study staff on patientpopulation and mechanism of action of the study medication.11
• -Evaluate subject safety and compliance with the study medication asspecified in the clinical research protocol.12
• Provide detailedstudy related documentation as required by the clinical researchtrial to ensure data integrity.13
• Adhere to reportingrequirements for safety reports, protocol noncompliance and anyother protocol required reports.14
• Ensure subject
• -s informedconsent is obtained appropriately throughout the duration of theclinical trial.15
• Adhere to the requirements detailed on the FDA1572 or Statement of Investigator form.16
• Collaborate with SiteLeadership to ensure operations goals are met.17
• Serve as a KeyOpinion Leader for psychiatric clinical research trials within theorganization and with key customers.18
• Attend InvestigatorMeetings and educational seminars
• –

Skills/Qualifications:

1

• Possess a valid M.D. or D.O. degree
• 2•BoardCertification gastroenterology•4•Active DEA license, orable to obtain one•-5•Active license to practice medicinein the state of Florida, or ability to obtain one immediately6•Strong interpersonal and leadership skills, self-motivation,and high personal integrity and ethics required•

Education andExperience:

• -1•Possess a valid MD or DO medical degree3•3-5years experience conducting clinical research trials as either a PIor Sub-investigator, or other relevant experience