Reference Number: JO-1912-441998
Job Type: Permanent
Location: United States
A full-service early phase CRO for the pharmaceutical, biotechnology and medical device industries is looking for a CA licensed Physician to serve as Clinical Investigator on their upcoming clinical trial programs. This is a great entry point into industry and offers Physicians a normal office hours schedule in Cypress, CA.
The Clinical Investigator – Physician will fulfill the role of Principal Investigator (PI) or Sub-Investigator (Sub-I) as the study dictates. The position is responsible for ensuring that the protocol is conducted to plan and according to all applicable regulations. The Physician will conduct clinical trials and provide oversight of subjects, clinical research staff and the management of data.
ESSENTIAL JOB FUNCTIONS
Responsible for protecting the rights, safety, and welfare of all subjects.
Provide both emergent and non-emergent medical care to subjects:
Attend meetings related to the study, such as but not limited to:
o Pre-study Meetings, Site Initiation Visits, and Investigator meetings.
o Dose Strategy Meetings
o Safety Review/Dose Escalation Meetings
o Monitor/Sponsor meetings and Close-Out Visit Meetings
Review and thoroughly understand all assigned protocols and study procedures.
Create a protocol synopsis with key relevant details of the protocol
Provide training on all assigned protocols and study procedures
Sign-off on the Delegation of Authority Log and delegating only those staff that are qualified and appropriately trained on the protocol.
Provide guidance to staff/recruitment and answer any protocol-related enrollment issues.
Responsible for discussing any medical or protocol-related issues with the medical monitor.
Current California License as a MD/DO
Experience as a Clinical Investigator is preferred though not essential
If youre seeking an opportunity into industry with interest in research and advancing global health, please apply. All inquiries to email@example.com / (617) 844-1436.