Find Jobs
Find Jobs Near You – Available Work in Your Location
Principal Investigator
Career Insights for Clinical Investigator
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Florida data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Clinical Investigator works on a clinical trial, and is responsible for ensuring that an investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations; for protecting the rights, safety, and welfare of subjects under the investigator's care; and for the control of drugs under investigation. The Clinical Investigator must also meet requirements set forth by the FDA, EMA or other regulatory body. The qualifications must be outlined in a current resume and readily available for auditors.
$171,041 / year median in Florida
+8% projected growth
Job Description
CareAccess.com. How This Role Makes a Difference We are seeking a highly skilled and experienced Principal Investigator to join our team. As the Principal Investigator, you will be responsible for oversight of all clinical trials according to study protocols, company processes, and GCP. How You'll Make An Impact Provide overall medical oversight and medical review of protocols in conformance with good clinical practice Review sponsor provided safety reports. Review and maintain accurate case report forms. Ensure that the safety and well-being of all participants in the study at the trial site are protected Assess subject response to therapy, evaluate and address adverse experiences Perform physical assessments, examinations and study procedures as required by study protocols Train Sub-Investigators and study staff members on protocol and protocol specific procedures. Provide medical support to sub-investigators and study staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. Review the inclusion/exclusion criteria, endpoint criteria, and investigational product use with the internal research team. Complete the necessary Care Access and protocol specific trainings Comply with ICH GCP (International Conference on Harmonization
- Good Clinical Practice) and all applicable regulatory requirements Participate in monitoring visits and sponsor meetings; allow monitoring and auditing by sponsors and inspection by appropriate regulatory agencies The Expertise Required Excellent written and verbal communication skills Ability to effectively prioritize tasks in a fast-paced environment Attention to detail and ability to maintain confidentiality when handling sensitive information.
Certifications/Licenses, Education, and Experience Minimum Education:
MD or DO with an active, unrestricted medical license (medical license must be valid in the state in which the research is conducted)Minimum Experience:
Previous experience as a Principal Investigator is required; 2 years prior experience as a Principal Investigator or Sub-Investigator, preferred Training and certification in Good Clinical Practice (GCP)How We Work Together Location :
Brandon, FL. This role requires 100% of work to be performed on site.Travel :
This is an onsite position with less than 10% travel requirements. Occasional planned travel may be required as part of the role. Physical demands associated with this positionInclude :
The ability to use keyboards and other computer equipment. Walking- 20% Standing
- 20% Sitting
- 20% Lifting
- 20% Up to 25 lbs Over 25 lbs Overhead Driving
- 20% Exposure to blood borne pathogens
- Yes The expected pay range for this role is $200,000
- $400,000 USD per year for full time team members.