Clinical Research Associate – United States (hiring in multiple locations across East & West Coast)
Help Deliver Better Clinical Research Outcomes
We are partnering with an innovative Contract Research Organization (CRO) to appoint Clinical Research Associates across multiple locations.
This opportunity is suited to clinical research professionals who enjoy working at the intersection of science, operations, and relationship management. You will play a key role in supporting the successful delivery of clinical studies by ensuring sites remain engaged, compliant, and operationally effective throughout the study lifecycle.
Whether your experience has been built within a CRO, sponsor, site environment, or a combination of settings, we are interested in speaking with individuals who thrive in dynamic clinical environments and enjoy building strong partnerships with investigators and study teams.
The Opportunity
As a Clinical Research Associate, you will support the planning, execution, monitoring, and close-out of clinical studies while maintaining the highest standards of quality, compliance, and patient focus.
You will act as a trusted point of contact across assigned sites and collaborate with cross-functional teams to drive study progress and deliver successful outcomes.
Key Responsibilities
- Conduct site initiation, monitoring, and close-out activities across assigned clinical studies
- Build effective relationships with investigators, site personnel, sponsors, and internal teams
- Monitor study conduct to ensure compliance with protocol requirements, GCP, ICH guidelines, SOPs, and applicable regulations
- Review study documentation and support timely, accurate data collection and issue resolution
- Identify risks proactively and partner with stakeholders to maintain study timelines and quality standards
- Support site engagement, recruitment planning, and operational readiness activities
- Maintain study documentation and contribute to inspection and audit readiness
- Provide clear communication and reporting on site performance and study progress
- Collaborate across clinical operations, data management, regulatory, and project teams to support delivery milestones
- Participate in process improvement initiatives and share best practices across programs
What We’re Looking For
- Previous experience within clinical research, clinical operations, or clinical study management
- Experience supporting or monitoring clinical studies in accordance with GCP and applicable regulations
- Strong organizational skills with the ability to manage multiple priorities simultaneously
- Excellent communication and stakeholder management capabilities
- Comfortable working independently while remaining highly collaborative
- Experience using CTMS, EDC, eTMF, or related clinical systems is advantageous
- Degree qualification preferred
- Willingness to travel based on study and regional requirements
Why Consider This Opportunity?
- Exposure to a diverse clinical research environment
- Opportunity to work across a broad portfolio of studies and programs
- Collaborative and supportive team culture
- Flexible working options depending on location and project requirements
- Career progression and professional development opportunities
If you are passionate about advancing clinical research and want to be part of studies that make a meaningful impact, we would love to hear from you.
Apply now or get in touch for a confidential conversation.