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Clinical Research Associate (CRA) -- CNS Trials | Northeast | 1099 Contract

GeoSera

Job Description

Location: Northeastern United States

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Engagement: Independent contractor (1099)

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Work arrangement: Field-based monitoring; travel required

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Compensation: Based on experience and agreed contract terms

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GeoSera is seeking an experienced Clinical Research Associate with demonstrable central nervous system (CNS) clinical trial monitoring experience.

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This opportunity is for a CRA who understands monitoring beyond completing visit reports: identifying site-level risks, maintaining oversight of trial conduct, resolving findings, and ensuring documentation and follow-up meet protocol and applicable regulatory requirements.

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Required qualifications

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  • Prior CRA experience in clinical research, with substantial hands-on CNS trial monitoring experience
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  • Experience conducting site initiation, routine monitoring, and close-out activities, as applicable to assigned studies.
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  • Working knowledge of ICH-GCP, protocol compliance, informed consent, source data review and verification, essential documents, and site oversight.
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  • Demonstrated ability to identify, document, escalate, and follow through on site issues and monitoring findings.
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  • Experience with clinical trial management systems (CTMS), electronic trial master files (eTMF), and electronic data capture (EDC) systems relevant to previous assignments.
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  • Availability for required site travel across the Northeastern United States.
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  • Ability to work under an independent 1099 contractor arrangement.
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Applications must demonstrate actual experience.

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Please submit the following:

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1. Current CV

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Include monitoring experience, CNS indications, trial phases, study types, sponsor/CRO experience, geographic coverage, and dates of relevant assignments.

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2. Documented CNS experience

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Identify the CNS indications and studies supported, your monitoring responsibilities, and the nature of your site oversight. Do not disclose confidential sponsor information or protected study data.

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3. Documented skills and achievements

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Provide two or three specific examples of professional results, such as resolving recurring site findings, improving follow-up timelines, addressing protocol deviations, supporting inspection readiness, or managing challenging sites. Include measurable outcomes where available.

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4. Monitoring and systems experience

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List relevant CTMS, EDC, eTMF, and other monitoring systems, along with your practical level of proficiency.

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5. Professional references

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Provide two relevant professional references who can verify your CRA performance and CNS trial experience. Obtain their permission before sharing their contact information.

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6. Contractor and travel availability

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Confirm your availability for 1099 work, your Northeast geographic coverage, and your ability to meet the required travel schedule.

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Applications that do not address the CNS experience requirement or provide the requested supporting information may not advance.

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GeoSera will evaluate candidates based on relevant trial experience, monitoring judgment, documentation quality, demonstrated results, and verifiable references.

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To apply: Submit your CV and supporting information through LinkedIn or the application channel specified by GeoSera.

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#ClinicalResearch #CRA #ClinicalResearchAssociate #CNS #ClinicalTrials #1099Contract #ClinicalOperations #ClinicalResearchJobs

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Vacancy posted 2 days ago
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