What are the responsibilities and job description for the Principal Investigator position at Kelly Science, Engineering, Technology & Telecom?
The Kelly FSP group is currently hiring for a Principal Investigator (MD, DO, NP, PA) to join one of our growing teams.
This Principal Investigator will be responsible for decentralized/hybrid clinical trials, and will function as a part of the Medical Affairs Department to provide medical and scientific support to different internal functional areas, clinical trial investigators/sites and study sponsors.
RESPONSIBILITES
- Function as PI or Sub-I for site based and/or decentralized/hybrid clinical trials, providing input into operational planning to ensure appropriate PI oversight with attention to patient safety and data integrity.
- Provide training as indicated to site staff in coordination with Site Director.
- Support and foster collaborative agreements and interactions with local practices/physicians/physician groups/medical providers to facilitate patient
- enrollment in coordination with the Site Director.
- Monitor Study Market Place for potential studies and respond to feasibilities in a timely manner.
- Maintain knowledge and clinical expertise in relevant therapeutic areas.
- Provides thorough review of protocol and other study materials
- Determines clinical and practical “fit” for our practice partner sites by assessing study complexity, logistics, etc.
- Collaborate with Trial Placement and Operations to determine which studies are appropriate for which sites/investigators
- Interact with potential, onboarding, and existing sites and investigators as requested by Research Operations, Decentralized Trial team and Site Account Managers.
- May travel to sites as needed
- Provide therapeutic and protocol specific training and supporting material for project teams and local investigators as indicated, and for internal operations needs
- Prepares risk assessment to determine potential pitfalls and issues that may occur during studies
- Participates in the development and medical review of recruitment and enrollment strategies and material.
- Provides medical and scientific knowledge on products and therapeutic areas to inform future growth.
- Interacts with outside medical experts as required.
- Provide input and participate in technology and other strategic committees as appropriate.
- Follows ethical and professional codes of conduct and escalate noncompliance as needed
- Comply with Clinic, and Sponsor policies, standard operating procedures (SOPs), GCP guidelines and documents data according to ALCOA.