What are the responsibilities and job description for the Trial Manager position at System One?
Title of Position: Clinical Trial Manager
Contract length: 12 months
Location: Ridgefield, CT
Schedule: hybrid; 2-3 days onsite
Hours: 40
Type: Contract
Overview
The CTM will be responsible for ensuring the quality execution of clinical studies, including study protocol and content form development, study budget management, and partnering with product and technology development. The ideal candidate will have expertise in both procedural work and application work, combining hands-on experimentation with scientific principles and knowledge from science/engineering education to solve technical problems. If you have a passion for clinical research and are looking for a challenging and rewarding opportunity, apply today!
Responsibilities
• Act as the main point of contact to Clinical Development & Operations for assigned trials.
• Responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration.
• Provide input to clinical trial protocols and bulk demands including comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies.
• Support investigations as Subject Matter Expert for assigned trials.
Requirements
Contract length: 12 months
Location: Ridgefield, CT
Schedule: hybrid; 2-3 days onsite
Hours: 40
Type: Contract
Overview
The CTM will be responsible for ensuring the quality execution of clinical studies, including study protocol and content form development, study budget management, and partnering with product and technology development. The ideal candidate will have expertise in both procedural work and application work, combining hands-on experimentation with scientific principles and knowledge from science/engineering education to solve technical problems. If you have a passion for clinical research and are looking for a challenging and rewarding opportunity, apply today!
Responsibilities
• Act as the main point of contact to Clinical Development & Operations for assigned trials.
• Responsible leader of the CTSU trial team within the matrix structure, ensuring cross-functional collaboration.
• Provide input to clinical trial protocols and bulk demands including comparator and non-IMP commercial products, to specific packaging designs and efficient distribution strategies.
• Support investigations as Subject Matter Expert for assigned trials.
Requirements
- Bachelor's degree in natural sciences
- Preferred is good knowledge and understanding of the regulatory and GMP/GCP requirements for IMPs
- Very good communication, negotiation and presentation skills
- Ability to work independently as well as in a team
- Fluency in written and spoken English
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