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Clinical Research Associate

Fortrea
1+ years
$105,000 – $118,000
Dallas, United States
1 June 9, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Interpersonal Skill, Labelling Assessment, MedDRA Coding

Clinical Research Associate II (Phase I)

Location: Dallas, TX / Remote (Kansas & United States)
Job Type: Full-Time
Job Requisition ID: 262566
Travel Requirement: 40–50% Overnight Travel
Compensation: $105,000 – $118,000 per year
Work Arrangement: Remote


About the Role

We are seeking an experienced Clinical Research Associate II (CRA II) with Phase I clinical research experience to join our growing team. The ideal candidate will possess strong site monitoring expertise, excellent clinical judgment, and the ability to manage multiple clinical trial activities while ensuring participant safety, regulatory compliance, and data integrity.

Candidates residing in the Midwest region are strongly preferred.


Key Responsibilities

Clinical Site Monitoring

  • Conduct all aspects of study site monitoring, including:

    • Pre-Study Visits (PSV)

    • Site Initiation Visits (SIV)

    • Routine Monitoring Visits

    • Close-Out Visits (COV)

  • Maintain study files and monitoring documentation.

  • Collaborate with vendors and study stakeholders throughout the clinical trial lifecycle.

  • Ensure study activities comply with protocol requirements, GCP guidelines, and applicable regulations.

Site Management

  • Manage assigned clinical sites according to project plans.

  • Monitor site performance, enrollment progress, and protocol compliance.

  • Identify, document, and escalate site-related issues when necessary.

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

Participant Safety & Regulatory Compliance

  • Verify that informed consent procedures are properly conducted and documented.

  • Ensure participant rights, safety, and well-being are protected throughout the study.

  • Confirm adherence to protocol requirements and regulatory standards.

  • Review site documentation for compliance with applicable regulations.

Data Review & Quality Assurance

  • Perform source data verification (SDV).

  • Review Case Report Forms (CRFs) and electronic data collection systems.

  • Identify missing, inconsistent, or implausible data.

  • Generate, manage, and resolve data queries according to study guidelines.

  • Ensure data accuracy and integrity throughout the trial.

Serious Adverse Event (SAE) Management

  • Review and process SAE reports.

  • Prepare SAE narratives and supporting documentation.

  • Follow up with study sites regarding SAE reporting requirements.

  • Ensure timely reporting in accordance with regulatory guidelines.

Registry & Feasibility Activities

  • Support registry management activities as outlined in project plans.

  • Conduct site feasibility assessments when required.

  • Evaluate site capabilities and recruitment potential.

Project Coordination

  • Serve as a Local Project Coordinator for assigned studies when applicable.

  • Act as a local client contact under supervision.

  • Coordinate study activities among internal and external stakeholders.

  • Assist in maintaining project timelines and deliverables.

Training & Mentorship

  • Support onboarding and training of new CRAs through co-monitoring activities.

  • Share best practices and provide guidance to junior team members.

  • Contribute to continuous process improvement initiatives.

Additional Duties

  • Perform other study-related responsibilities as assigned by management.


Required Qualifications

Education

  • Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related healthcare discipline

OR

  • Certification in an allied health profession from an accredited institution (e.g., Nursing Licensure)

Experience

  • Minimum 1 year of Clinical Monitoring experience.

  • Prior Phase I clinical research experience required.

  • Experience conducting independent site monitoring visits.