$120K/yr – $130K/yr
You'll complete your application on the employer's website.
Job type
Salary
$120K/yr – $130K/yr
Sector
Posted
18 days ago
Responsibilities
Conduct site selection, initiation, monitoring, and close-out visits to ensure compliance with GCP, ICH, protocol requirements, and applicable regulatory standards
Partner with investigative sites to develop, track, and execute patient recruitment and enrollment strategies to meet study objectives and timelines
Deliver protocol and study-specific training, maintain ongoing communication with site personnel, and proactively address operational issues and risks
Monitor study conduct and site performance, assess protocol adherence, identify quality concerns, and escalate issues to support regulatory compliance and data integrity
Track study milestones including regulatory submissions, site activation, patient recruitment, enrollment, and data management activities to ensure successful study execution
Maintain essential trial documentation within TMF and ISF files, support site financial management and invoice processing, and mentor clinical staff through training, co-monitoring, and collaborative study support
Preferred
Bachelor's degree in a scientific, life sciences, healthcare, or related discipline preferred
Benefits
Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
Zachary Piper Solutions is an IT company providing government contracting solutions in support of the nation’s Intelligence Community.
Mclean, Virginia, USA
http://zacharypiper.com/
Growth Stage
Total Funding
$3M
2018-02-22
Series Unknown· $1.3M
2014-04-10
Series Unknown· $1.7M
Leadership Team
Justin Jordan
Founder and Chairman
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Qualifications
Minimum of 3 years of recent on-site clinical monitoring experience in Oncology, with direct experience supporting Phase I studies involving solid and/or liquid tumor indications; this requirement is mandatory
Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, regulatory requirements, and oncology clinical trial protocols
Proven ability to independently manage investigative sites, monitor study conduct, ensure protocol compliance, and maintain high standards of data quality and patient safety
Proficiency with Microsoft Office applications, along with excellent communication, organizational, problem-solving, and relationship-management skills
Demonstrated ability to effectively manage timelines, budgets, and competing priorities while building strong collaborative partnerships with investigators, site personnel, and cross-functional study teams
Bachelor's degree in a scientific, life sciences, healthcare, or related discipline preferred
Minimum of 3 years of recent on-site clinical monitoring experience in Oncology, with direct experience supporting Phase I studies involving solid and/or liquid tumor indications; this requirement is mandatory.
Required skills
Oncology Clinical Trials, Phase I Oncology Trials, Clinical Site Monitoring, Clinical Practice (GCP), ICH Guidelines, Oncology Clinical Trial Protocols, Microsoft Office, Relationship Management
Experience
3+ years
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