Quick overview
Job description
Job Title: Senior Clinical Trial Manager - Remote / Telecommute
Job Location: Ridgefield, CT
Job Type: Contract
Pay Range: $67.50hr - $72.50hr
Job Overview:
The Clinical Trial Manager (CTM) is accountable for the operational management of the local component of a clinical trial, ensuring trial recruitment commitments, timelines, budgets, and quality standards are met. The candidate supports the local trial team to ensure the integrity of trial conduct, patient safety, and adherence to regulatory requirements through effective planning, conduct, and closeout. Working within a complex Google Cloud Platform environment on global clinical trials, the successful candidate will collaborate with multidisciplinary international teams and key stakeholders. The candidate will represent the organization at internal and external meetings and may be involved in designing and implementing new innovative methods as part of a working group.
Trial Preparation, Conduct and Closeout:
- In collaboration with Site Monitoring Lead and CRAs, ensure effective trial planning, execution, and closure.
- Serve as the primary trial contact for CRAs, investigators, and site staff.
Skills:
- Experience running pediatric clinical trials from initial start-up to completion.
- Strong communication skills in complex cross-functional matrix structures, articulating and aligning business strategy on an ongoing basis while demonstrating cultural sensitivity.
- Solid project management, networking, stakeholder management, and team leadership capability, with a thorough understanding of the scientific and technical components of clinical development.
- Demonstrated technical expertise across all aspects of clinical trial operations and execution, with the ability to work across several studies and therapeutic areas.
- Strong leadership and influence skills to address complex situations, resolve conflicts, and influence horizontally and vertically.
- Strategic mindset with the ability to embrace cross-functional initiatives, apply innovative learnings, identify risks, and plan mitigation.
- Proficiency in coordination and oversight, setting priorities, managing the pace of activities, and ensuring efficient usage of resources.
Education:
- Bachelor s degree plus 6+ years of experience in clinical research, preferably in the pharmaceutical industry.
- Master s degree or PharmD plus 4+ years of experience in clinical research, preferably in the pharmaceutical industry.
- PhD or MD plus 2+ years of experience in clinical research, preferably in the pharmaceutical industry.
== ==
- Medical, Dental, and Vision Insurance
- 401(k) Retirement Plan
- Health Savings Account (HSA)
- Disability Insurance (Short-Term and Long-Term)
- Life and AD&D Insurance
- Paid Sick Leave (where required by applicable state or local law)
- Supplemental Insurance Plans
- Identity Theft Protection
- Pet Insurance
- Employee Wellness Programs
- Employee Assistance Program (EAP)
- Career Growth and Professional Development Opportunities
About Cynet Systems
Founded in 2010 and headquartered in the Washington, DC metro area, Cynet Systems Inc. is a leading technology staffing and workforce solutions company serving Fortune 500 companies, government agencies, and enterprise organizations across the United States and Canada. We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and professional staffing, powered by a high-performing recruitment engine operating across North America and Asia.
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