Full-time
In-House Clinical Research Associate - 175520 - 176208
$50K/yr – $80K/yr
Bethesda, MDScience & PharmaceuticalPosted 17d ago
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Role overview
Job type
Salary
$50K/yr – $80K/yr
Location
Sector
Posted
17 days ago
Job description
Piper Companies is recruiting an In-House Clinical Research Associate for a mission-driven organization focused on healthcare innovation. The role supports clinical research operations by managing project documentation, coordinating with sites and stakeholders, and maintaining records and workflow tracking systems.
Tags
Government
Information Technology
Software
Information Services
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Responsibilities
Review and manage project documentation to ensure accuracy, completeness, and compliance
Coordinate with sites and stakeholders to obtain missing information and resolve documentation-related inquiries
Maintain organized electronic records, files, and tracking systems throughout the project lifecycle
Monitor document status and workflow progress within centralized databases and internal platforms
Support administrative and operational processes through accurate recordkeeping and data management
Preferred
Experience supporting IRB submissions or regulatory review processes preferred
Benefits
Medical
Dental
Vision
401K
Sick Leave as required by law
Hybrid work
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
3-5 years of clinical research experience, including document management and electronic systems support
Experience reviewing and maintaining regulatory documentation in a sponsor, CRO, research, or healthcare setting
Knowledge of clinical research regulations, compliance requirements, and documentation practices
Bachelor's degree in a science, health-related, or similar field
Experience supporting IRB submissions or regulatory review processes preferred
3-5 years of clinical research experience, including document management and electronic systems support.
Required skills
Clinical Research, Regulatory Documentation, Clinical Research Regulations, IRB Submissions
Experience
3-5 years
Interested in this role?
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