Clinical Research Associate Job at Parexel, USA | Life Sciences Candidates, Apply Now

Clinical Research Associate Job at Parexel, USA | Life Sciences | Apply Now

If you are an experienced clinical operations professional or an analytical life scientist looking to secure a high-impact, home-based position with a premier global biopharmaceutical partner, this opportunity at Parexel is an exceptional career move. Available as a fully remote role across all United States locations—with a strong regional node in North Carolina—this position inserts you directly into the frontline management of international, sponsor-dedicated clinical networks. For detail-oriented monitoring experts searching for a high-value Clinical Research Associate Job, this role offers total operational ownership over Risk-Based Quality Management (RbQM), electronic Trial Master File (eTMF) curation, and full site-lifecycle governance. It serves as an elite launchpad to advance a long-term Parexel career and stands out as a premier choices for anyone tracking a competitive Life Sciences Job within a leading Functional Service Provider (FSP) framework.

• Job Position: Senior Clinical Research Associate/Clinical Research Associate – All US Locations – FSP
• Location: United States, North Carolina (Remote)
• Job ID: R0000042560
• Category: Clinical Trials

About The Company

Parexel is a world-leading global Contract Research Organization (CRO) and healthcare intelligence powerhouse driven by a unified mission to prevent, treat, and cure diseases by getting innovative therapies to patients sooner. Spanning foundational science to late-stage commercialization, Parexel orchestrates complex Phase I–IV clinical development systems, specialized decentralized trial strategies, and real-world data frameworks for biopharmaceutical innovators worldwide. This position operates within Parexel Strategic Solutions, utilizing a Functional Service Provider (FSP) model. Under this strategic framework, you are deployed directly into a single, top-tier global pharmaceutical sponsor’s clinical portfolio. This model grants you the unique operational advantage of focusing deeply on a unified set of sponsor SOPs, specific therapeutic programs, and proprietary data monitoring systems—all backed by the global scale, administrative stability, and career progression pathways of a career at Parexel.

Remote Clinical Research Associate Job – Key Responsibilities

The Senior CRA / CRA II assumes local responsibility for the operational execution, compliance, and clinical data integrity of allocated investigative sites, acting as the primary hub contact for the Local Study Team (LST).

Your core site management, document auditing, and milestone verification duties include:

• Risk-Based Monitoring Execution: Conducting comprehensive onsite and remote monitoring visits, performing intensive remote data checks in strict accordance with the study-specific Monitoring Plan.
• Data Validation & Verification: Executing complex Source Data Review (SDR), Case Report Form (CRF) audits, and comprehensive Source Data Verification (SDV) to ensure robust clinical data quality.
• Site Activation & Qualification: Contributing to the selection of potential investigators, conducting Site Qualification Visits (SQV), and executing site initiation (SIV) and close-out (COV) phases.
• eTMF Architecture Maintenance: Documenting and uploading essential files into the electronic Trial Master File (eTMF) in real-time alignment with international ICH-GCP rules and sponsor guidelines to advance this Clinical Research Associate Job.
• Investigator & Staff Training: Training, supporting, and advising site investigators on protocol parameters and Risk-Based Quality Management (RbQM) principles to preserve absolute inspection readiness.
• Safety & Deviation Triage: Securing the accurate, timely reporting of Serious Adverse Events (SAEs) and their corresponding clinical follow-ups, while escalating systematic compliance or data privacy breaches.
• Supply & Drug Accountability: Managing the chain of custody for critical study drug supplies, overseeing investigator site files (ISF), and prepping expired or unused investigational products for witnessed destruction to support this Life Sciences Job.

Qualifications & Profile Requirements For Remote Clinical Research Associate Job

Parexel seeks inquisitive, self-starting, and highly analytical clinical researchers who demonstrate an compromise-free attention to detail and the capability to drive site performance independently.

• Required Academic Criteria:
  • Educational Foundation: A mandatory Bachelor’s degree in a related scientific discipline, preferably in the Life Sciences, or an equivalent qualification calibrated to successful clinical trial conduct.
• Essential Knowledge & Experience:
  • Regulatory Grounding: Excellent, working knowledge of international ICH-GCP guidelines, combined with a basic functional understanding of Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).
  • Clinical Operations Fluency: Strong, practical understanding of clinical study management mechanics, including remote data management, source documentation, and drug handling.
  • Language Proficiency: Complete professional fluency in written and spoken English is mandatory for building a strong Parexel career.
  • Technical Aptitude: Comfort navigating electronic Clinical Trial Management Systems (CTMS), remote monitoring tools, and automated dashboard frameworks.
• Desirable Competencies & Mobility:
  • Familiarity with risk-based monitoring frameworks and centralized statistical tracking tools.
  • Proven capability to prioritize and manage multiple clinical sites with conflicting deadline matrices.
  • Mobility Credentials: Possession of a valid domestic driving license, with the complete flexibility to travel nationally or internationally as required by monitoring plans.

In short, the Senior CRA / CRA position at Parexel is a definitive route to transitioning your scientific background into a premium global clinical asset. Securing an appointment here allows you to bypass general transactional monitoring and take centralized, strategic charge of the RbQM systems, eTMF workflows, and investigator relationships that advance life-saving therapies safely through US clinical pipelines. If you reside in the United States, meet the bachelor’s science requirements, and possess an compromise-free commitment to patient safety and data integrity, apply today to secure this premier Clinical Research Associate Job, launch an exceptional Parexel career, and lock in this outstanding Life Sciences Job.

APPLY ONLINE HERE