Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Clinical Research Associate - Texas/Central Us - Fsp

Parexel
5+ years
$120,000 – $155,000
Texas, Remote
1 June 30, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Senior Clinical Research Associate (CRA)

Company: Parexel
Location: Texas / Central US (Remote)
Department: Clinical Operations
Job Type: Full-Time
Work Mode: Remote (Field-Based)

JOB OVERVIEW

The Senior Clinical Research Associate (CRA) is responsible for independently managing clinical trial monitoring activities to ensure patient safety, data integrity, and regulatory compliance throughout the study lifecycle. The role involves site qualification, initiation, routine monitoring, close-out visits, oversight monitoring of CRO-managed sites, source data verification, drug accountability, regulatory documentation, issue management, inspection readiness, and collaboration with cross-functional clinical teams to ensure successful delivery of Phase I Oncology and other clinical studies in accordance with ICH-GCP, FDA regulations, and company SOPs.


KEY RESPONSIBILITIES

Clinical Site Monitoring

  • Conduct site qualification, initiation, interim monitoring, and close-out visits.

  • Perform both on-site and remote monitoring activities.

  • Ensure protocol compliance and patient safety throughout study execution.

  • Verify source data and ensure data accuracy using ALCOA principles.

  • Monitor site performance and study progress against project timelines.

Site Management

  • Build and maintain strong relationships with investigators and site staff.

  • Support site activation activities in collaboration with study teams.

  • Ensure investigator sites comply with ICH-GCP, regulatory requirements, and study protocols.

  • Monitor site documentation and regulatory compliance.

  • Coordinate study-related activities with investigator sites.

Oversight Monitoring

  • Develop and maintain Oversight Monitoring Plans.

  • Review CRO CRA performance and operational study metrics.

  • Conduct oversight monitoring visits independently or alongside CRO monitors.

  • Evaluate investigator site performance using key performance metrics.

  • Recommend corrective actions based on monitoring observations.

Drug Accountability & Investigational Product Management

  • Perform investigational product accountability and reconciliation.

  • Verify proper storage, handling, shipment, and destruction of study drugs.

  • Ensure compliance with investigational product management procedures.

  • Maintain complete drug accountability records.

  • Resolve investigational product discrepancies.

Documentation & Reporting

  • Prepare accurate monitoring visit reports.

  • Complete oversight monitoring reports within required timelines.

  • Maintain complete site regulatory documentation.

  • Verify timely submission of study documentation and safety reports.

  • Ensure Trial Master File (TMF) documentation is inspection-ready.

Issue Management

  • Identify protocol deviations and compliance issues.

  • Track study risks, issues, and corrective actions.

  • Escalate significant findings to study management.

  • Support implementation of corrective and preventive actions (CAPA).

  • Monitor issue resolution through study completion.

Cross-Functional Collaboration

  • Collaborate with Clinical Trial Liaisons (CTLs), Clinical Operations, Central Monitors, and CRO partners.

  • Participate in study team meetings and project discussions.

  • Support process improvement initiatives.

  • Communicate study updates to internal and external stakeholders.

  • Foster effective collaboration across global clinical teams.

Inspection Readiness

  • Support regulatory inspections and audit readiness.

  • Ensure investigator sites maintain complete and compliant documentation.

  • Verify inspection-ready clinical records.

  • Promote data integrity and quality throughout the study lifecycle.

  • Ensure compliance with FDA, EMA, PMDA, ICH-GCP, and company SOPs.


EDUCATIONAL QUALIFICATIONS

Required

Bachelor's Degree in:

  • Pharmacy (B.Pharm / M.Pharm)

  • Life Sciences

  • Biotechnology

  • Nursing

  • Medicine

  • Biomedical Sciences

  • Or a related healthcare discipline


EXPERIENCE REQUIREMENTS

Required

  • Minimum 5 years of Clinical Research Associate (CRA) monitoring experience.

  • Experience in Phase I Oncology Clinical Trials.

  • Experience conducting:

    • Site Qualification Visits (SQV)

    • Site Initiation Visits (SIV)

    • Routine Monitoring Visits (RMV)

    • Close-Out Visits (COV)

  • Experience with CRO oversight monitoring.

  • Willingness to travel for SWAT assignments and oversight monitoring visits.

Preferred Experience

  • Oncology clinical trials.

  • Global clinical trial monitoring.

  • Investigator site management.

  • Clinical Operations.

  • Inspection and audit readiness.

  • FDA, EMA, and PMDA regulated studies.