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Cra Manager Jobs in Raleigh, NC (NOW HIRING)

Aquent

DevSecOps Engineer

Raleigh, NC · On-site +1

$55 - $60/hr

Contribute to a central vulnerability and waiver database supporting consistent risk-acceptance management, audit traceability, and long-term reporting * Translate CRA regulatory requirements into ...

Icon plc

Senior Clinical Research Associate

Cary, NC · Remote

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will ...

Allucent

Clinical Trial Leader

Cary, NC · On-site +1

Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Managerand other functional leadsto ensureclinical monitoringdeliverables (timeline, budget, quality ...

Allucent

Clinical Trial Leader

Cary, NC · Remote

Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Manager and other functional leads to ensure clinical monitoring deliverables (timeline ...

Allucent

Clinical Trial Leader

Cary, NC · On-site +1

Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Manager and other functional leads to ensure clinical monitoring deliverables (timeline, budget ...

Neshent Tech

Coupa Solution Architect

Raleigh, NC

$61.25 - $80.75/hr

Coupa Supplier Information Management (SIM) * Coupa Platform Certification * Coupa CSO ... Provide expertise across Coupa Core, Strategic Sourcing, CSO, CLM-S, CLM-A, RPM-A (SIM & CRA ...

Syneos Health

CTM - Future Roles (US)

Morrisville, NC · On-site

For Real World Late Phase, the CRA I will use the business card title of Site Management Associate I. Additional responsibilities include: Site support throughout the study lifecycle from site ...

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Cra Manager information

What is the difference between Cra Manager vs Clinical Research Associate?

AspectCra ManagerClinical Research Associate
CredentialsBachelor's or higher in life sciences, often with experience in project managementBachelor's degree in life sciences or related field, often with certification
Work EnvironmentLeads multiple studies, manages teams, oversees project progressMonitors clinical trials at sites, ensures protocol compliance
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical sites
Search & Comparison IntentHigher-level management, overseeing clinical trialsMonitoring and site management roles

The Cra Manager typically oversees multiple clinical trials, manages teams, and ensures project milestones are met, requiring leadership skills and experience. In contrast, a Clinical Research Associate focuses on monitoring individual trial sites, ensuring compliance with protocols. Both roles are essential in clinical research but differ in scope and responsibilities.

What is a CRA Manager?

A CRA Manager, or Clinical Research Associate Manager, is a professional responsible for overseeing a team of Clinical Research Associates (CRAs) who monitor clinical trials. They ensure that clinical studies are conducted in compliance with regulatory standards, protocols, and company policies. CRA Managers coordinate training, provide performance feedback, and act as a liaison between CRAs, sponsors, and other stakeholders. Their role is critical in maintaining the quality and integrity of clinical research projects.

What are some common challenges a CRA Manager faces when overseeing multiple clinical trial sites?

A CRA Manager often encounters challenges with maintaining consistent quality and compliance across various clinical trial sites, as each site may have unique operational practices and resource limitations. Effective communication and coordination between on-site teams, sponsors, and regulatory bodies are crucial to address issues promptly and ensure study timelines are met. Additionally, balancing the workload among Clinical Research Associates (CRAs) and providing adequate training and support can be demanding, especially when managing geographically dispersed teams.

What are the key skills and qualifications needed to thrive as a CRA Manager, and why are they important?

To thrive as a CRA (Clinical Research Associate) Manager, you need a deep understanding of clinical trial processes, regulatory requirements, and a relevant life sciences degree, often supplemented by experience as a CRA. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications such as ACRP or SOCRA are typically required. Leadership, strong communication, and problem-solving skills help you guide teams and ensure effective collaboration across stakeholders. These skills are crucial for maintaining compliance, ensuring data integrity, and delivering successful clinical trials on time and within budget.
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Cra Manager jobs near you
Infographic showing various Cra Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.
DevSecOps Engineer

DevSecOps Engineer

Aquent

Raleigh, NC • On-site, Remote

$55 - $60/hr

Temporary

Posted yesterday

Job description

Placement Type:
N/A
Salary:
$55-60 Hourly
Start Date:
May 11, 2026
We are seeking a senior DevSecOps engineer for direct assignment to one of our enterprise clients - a global test-and-measurement and instrumentation OEM with a broad portfolio of embedded and long-lifecycle products. The engagement supports the client's initiative to achieve compliance with the EU Cyber Resilience Act (CRA) ahead of the December 2027 enforcement date. This requisition is for the US Citizen seat on a three-person engineering team. The selected candidate will be the team's designated US-based resource and must be a
US Citizen - Lawful Permanent Residents do not qualify for this role.
Scope & Environment
The work introduces security controls into an existing and diverse product ecosystem rather than building greenfield solutions. Expect:
  • A broad portfolio of products across embedded systems and long-lifecycle device lines
  • A large number of repositories, including legacy codebases predating modern DevSecOps/CI/CD practices
  • High heterogeneity: multiple build systems, toolchains, and packaging processes - standard, custom, and vendor-specific
  • Continuous balancing of regulatory compliance (CRA), engineering pragmatism, and portfolio-wide scalability
  • Solutions must be long-term maintainable, auditable, and reusable across teams

What the Engineer Will Do
  • Implement and scale SAST and SCA across heterogeneous and often legacy codebases
  • Generate and maintain Software Bills of Materials (SBOMs)
  • Integrate security tooling into multiple build systems and CI/CD pipelines, including vendor-specific and custom toolchains
  • Design scalable, reusable security workflows applicable across many repositories and product teams
  • Contribute to a central vulnerability and waiver database supporting consistent risk-acceptance management, audit traceability, and long-term reporting
  • Translate CRA regulatory requirements into concrete, engineering-pragmatic technical controls
  • Drive end-to-end ownership of initial priorities: rapid implementation of security scanning and full visibility of current security posture

Required Experience
  • Demonstrable product-security or regulated-compliance background (CRA, IEC 62443, FDA, DoD, ISO 27001, or similar) with the ability to translate regulation into technical solutions
  • Hands-on, production-scale experience with SAST and SCA tools (e.g., Veracode, CodeSonar)
  • Practical experience generating and maintaining SBOMs
  • CI/CD build and automation across GitHub, GitLab, GitHub Actions, and AWS
  • Working knowledge of C and C++
  • Working knowledge of Python (automation scripts, supporting tools)
  • Experience integrating security into multiple build systems and toolchains (CMake, Make, vendor-specific)
  • Track record scaling security workflows across portfolios with many repositories and a mix of legacy and greenfield work
  • Experience designing or contributing to vulnerability, waiver, or risk-acceptance databases
  • Awareness of embedded systems and long-lifecycle product constraints

Preferred (Nice-to-Have)
  • Prior exposure to semi-automated or AI-assisted vulnerability remediation workflows (as engineering support, not replacement for engineering decisions)
  • Previous DevSecOps work at OEMs with broad hardware portfolios
  • Familiarity with federal or highly regulated industries

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