Skip to main content
McCarthy Search

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

L5

geoseraLexington, KY7 days ago

Occupations

Clinical Research CoordinatorsGeodetic SurveyorsRegulatory Affairs Specialists

Industries

Research and Development in the Physical, Engineering, and Life SciencesOther Scientific and Technical Consulting ServicesResearch and Development in Biotechnology
Location: Northeastern United States
Engagement: Independent contractor (1099)
Work arrangement: Field-based monitoring; travel required
Compensation: Based on experience and agreed contract terms
GeoSera is seeking an experienced Clinical Research Associate with demonstrable central nervous system (CNS) clinical trial monitoring experience. 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.
Required qualifications:
  • Prior CRA experience in clinical research, with substantial hands-on CNS trial monitoring experience
  • Experience conducting site initiation, routine monitoring, and close-out activities, as applicable to assigned studies.
  • Working knowledge of ICH-GCP, protocol compliance, informed consent, source data review and verification, essential documents, and site oversight.
  • Demonstrated ability to identify, document, escalate, and follow through on site issues and monitoring findings.
  • Experience with clinical trial management systems (CTMS), electronic trial master files (eTMF), and electronic data capture (EDC) systems relevant to previous assignments.
  • Availability for required site travel across the Northeastern United States.
  • Ability to work under an independent 1099 contractor arrangement.
  • Applications must demonstrate actual experience.
  • Please submit the following:1. Current CVInclude monitoring experience, CNS indications, trial phases, study types, sponsor/CRO experience, geographic coverage, and dates of relevant assignments.2. Documented CNS experience
  • 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.3. Documented skills and achievements
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.4. Monitoring and systems experience List relevant CTMS, EDC, eTMF, and other monitoring systems, along with your practical level of proficiency.5. Professional references Provide two relevant professional references who can verify your CRA performance and CNS trial experience. Obtain their permission before sharing their contact information.6. Contractor and travel availability Confirm your availability for 1099 work, your Northeast geographic coverage, and your ability to meet the required travel schedule. Applications that do not address the CNS experience requirement or provide the requested supporting information may not advance. GeoSera will evaluate candidates based on relevant trial experience, monitoring judgment, documentation quality, demonstrated results, and verifiable references. To apply: Submit your CV and supporting information through LinkedIn or the application channel specified by GeoSera.#Clinical Research #CRA #Clinical ResearchAssociate #CNS #Clinical Trials #1099 Contract #Clinical Operations #Clinical ResearchJobs
Apply now (opens in a new tab)
Apply now (opens in a new tab)

Level

SeniorL5

Location

Lexington, KY

Occupation

Clinical Research Coordinators

Industry

Research and Development in the Physical, Engineering, and Life Sciences

Posted

7 days ago

To get sharper similar jobs, create your profile using the link below.

Create profile