Physician / Neurology / Florida / Permanent / Neurologist Physician -

Benefits

Qualifications

• •Actively work to receive and maintain certification for all required rating scales Skills/Qualifications:1
• •Possess a valid M.D. or D.O. degree 2
• •Board Certification in Neurology 4
• •Active DEA license, or able to obtain one 5
• •Active license to practice medicine in 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 and Experience: 1
• •Possess a valid MD or DO medical degree2
• •Board certification in neurology3
• •3-5 years experience conducting neurology clinical research trials as either a PI or Sub-investigator, or other relevant experience
• •6 more items(s)

Responsibilities

• •Position Summary: Neurologist will serve as a Principal or Sub-Investigator for clinical trials with pharmaceutical companies testing new medications
• •The Principal Investigator is responsible for conducting clinical trials in accordance with the research protocol, Good Clinical Practices (GCPs), and federal/state regulations
• •Job Responsibilities: 1. Maintain current license to practice medicine
• •Assume responsibility as the Principal or Sub-Investigator for the duration of clinical trials.3
• •Strong working knowledge of regulatory requirements and GCP standards.4. Possess thorough understanding of the clinical research protocol and patient population for which the trial is designed.5. Perform evaluations.6. Complete training as required per sponsors vendors to obtain certification to conduct testing and rating scales for specific protocols.7
• •Conduct testing and rating scales per sponsors instructions and protocols
• •Completion of all documentation, paper and electronic, as required per protocol.8. Evaluate subjects for clinical research trials based on their past medical history in comparison to the protocol specific inclusion and exclusion criteria.9
• •Ensure appropriate delegation and training of the clinical research staff.10
• •Educate study staff on patient population and mechanism of action of the study medication.11
• •Evaluate subject safety and compliance with the study medication as specified in the clinical research protocol.12
• •Provide detailed study related documentation as required by the clinical research trial to ensure data integrity.13
• •Adhere to reporting requirements for safety reports, protocol noncompliance and any other protocol required reports.14
• •Ensure subjects informed consent is obtained appropriately throughout the duration of the clinical trial.15
• •Adhere to the requirements detailed on the FDA 1572 or Statement of Investigator form.16. Collaborate with Site Leadership to ensure operations goals are met.17
• •Serve as a Key Opinion Leader for psychiatric clinical research trials within the organization and with key customers.18
• •Attend Investigator Meetings and educational seminars
• •Testing and Rating Scales Required:1
• •Meet or exceed study sponsor minimum qualifications needed for all identified rating scales2
• •15 more items(s)