Clinical Trial Manager
Contract W2
On-site
$50 - $60/hr
Talent Software Services, Inc
Fitment
Dice Job Match Score™
👾 Reticulating splines...
Job Details
Skills
- CLINICAL TRIAL
- CLINICAL STUDY
- HUMAN STUDY
- HUMAN TESTING
- GOOD CLINICAL PRACTICE
- GCP
- ICH-GCP
- ICH
Summary
Clinical Trial Manager
Job Summary: Talent Software Services is in search of a Clinical Trial Manager for a contract position in Mason, OH. The opportunity will be for 12 months with a strong chance for a long-term extension.
Primary Responsibilities/Accountabilities:
Qualifications:
If this job is a match for your background, we would be honoured to receive your application!
Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities, including contract, contract to hire, and permanent placement. Let''s talk
Job Summary: Talent Software Services is in search of a Clinical Trial Manager for a contract position in Mason, OH. The opportunity will be for 12 months with a strong chance for a long-term extension.
Primary Responsibilities/Accountabilities:
- 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-Google Cloud Platform 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.
Qualifications:
- 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.
If this job is a match for your background, we would be honoured to receive your application!
Providing consulting opportunities to TALENTed people since 1987, we offer a host of opportunities, including contract, contract to hire, and permanent placement. Let''s talk
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
- Dice Id: talmn001
- Position Id: 26-02924
- Posted 15 hours ago
Company Info
We pride ourselves in making sure that diversity in the workplace is at the forefront of our business. Our Founder, Dave Iacarella, is an Army Veteran who is committed to giving back to fellow Veterans. We are proud of our history of transitioning military Veterans into the workforce with companies that value their service. TALENT helps companies meet their veteran and diversity spend initiatives and requirements. We are committed to supporting veteran and diverse organizations.
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