Senior Clinical Research Associate at Jobgether – United States
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About This Position
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Clinical Research Associate in United States.
This Senior Clinical Research Associate role is focused on supporting and executing high-quality clinical trial monitoring and site management activities across the United States.
The position plays a key role in ensuring studies are conducted in compliance with ICH-GCP, local regulations, and study protocols.
You will work closely with investigator sites and cross-functional clinical teams to ensure smooth study execution and timely delivery of milestones.
The role includes both on-site and remote monitoring, with frequent travel and strong engagement with site personnel.
You will also contribute to oversight activities, ensuring CRO partners and sites maintain data integrity and operational quality.
This is a highly collaborative and impact-driven position within a global clinical research environment focused on improving patient outcomes.
It offers exposure to complex studies and the opportunity to directly influence the quality and success of clinical development programs.
- Execute site monitoring activities including qualification, initiation, interim, and close-out visits, ensuring compliance with protocols, ICH-GCP, and regulatory standards
- Manage site relationships, maintaining effective communication and supporting issue resolution throughout the study lifecycle
- Conduct oversight monitoring activities, including review of CRO CRA performance, study metrics, and site-level deliverables
- Perform drug accountability, reconciliation, and ensure proper handling, storage, and destruction processes
- Review source documentation and ensure accurate and complete data capture aligned with ALCOA principles
- Prepare, write, and submit detailed monitoring visit reports, oversight reports, and study correspondence
- Identify protocol deviations, escalate non-compliance issues, and ensure appropriate corrective actions are implemented
- Collaborate with clinical teams, CTLs, and CRO partners to support study activation, execution, and inspection readiness
Requirements:
- Bachelor’s degree or equivalent in a scientific or health-related field
- Minimum of 5 years of experience as a Clinical Research Associate or in a related clinical research role
- Strong knowledge of clinical drug development processes and ICH-GCP guidelines
- Familiarity with regulatory frameworks such as FDA, EMA, and PMDA requirements
- Experience with clinical systems including EDC, CTMS, and Microsoft Office applications
- Strong analytical thinking, problem-solving skills, and attention to detail
- Excellent communication and interpersonal skills to manage stakeholder relationships effectively
- Strong organizational skills with the ability to prioritize tasks and manage travel-intensive workloads
- Ability to produce clear, concise, and high-quality written reports
Benefits:
- Competitive compensation aligned with experience and market standards
- Comprehensive health, dental, and vision insurance coverage
- Retirement savings plans with employer contributions
- Flexible work arrangements with significant travel opportunities across the United States
- Opportunities for professional development and continued training in clinical research
- Exposure to global clinical trials and cross-functional collaboration
- Supportive and inclusive work environment focused on innovation and impact in healthcare.