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Clinical Trial Manager

|  Posted On: Mar 13, 2026

location:Mason, OH 45040

Duration:12 Months, Contract

mode of work:On-site

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Job Summary

Job Title:  
Clinical Trial Manager
Posted Date:  
Mar 13, 2026
Duration:  
12 Months, Contract
Shift(s):  

08:00 - 16:00

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Name:
 
Vikramsinh Thakor

Email:
 
vikramsinh@rangam.com

Phone:
 
678-922-5008

Description

20 Hrs a week

 

Must Have

  • Familiar with Budgets, contracts and deploying Informed Consents
  • Flexible Schedule - Able to work both remotely and onsite, work 2-3 consecutive days a week
  • Previous Clinical trial manager role and can lead a small team

 

Job Description

  • Procedural work and expertise in Application work by combining hands-on experimentation with scientific principles and knowledge from science/engineering education to drive foundational technical understanding and solve technical problems.
  • Delivers technical outputs which address critical innovation challenges and completion of key milestones.
  • The Clinical Trial Manager (CTM) is a key member of the clinical team with responsibility for defining and managing the quality execution of clinical studies.
  • Partner closely with product and technology development to design and execute clinical studies for claims support, credentialing, decision making, and fundamental understanding.
  • The CTM role is pivotal for driving robust human testing and clinical trials that are compliant with established governance principles, including ICH-GCP Guidelines.

 

Responsibilities:

  • Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key components of a successful clinical trial.
  • Management of study logistics, timelines, and budget/expense tracking.
  • Prepare documentation for study placement and clearances, clinical trial protocols, and IRB submissions, as needed.
  • Conduct study close out and tasks, including documentation and archiving of study materials.
  • Contribute to the development of Standard Operating Procedures and adhere to all aspects of Governance and Quality systems.
  • Represent clinical operations are regulatory meetings, sponsor meetings, and any other multifunctional meetings, as needed.

 

Skills:

  • Experience in human testing and the management of Clinical Trials, including a fundamental knowledge of Good Clinical Practices.
  • The candidate will have a strong background in a fundamental knowledge of Biology, Chemistry and/or measurement science.