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Fsp - Sr Cra 2 - Midwest, Arizona, Texas, New Mexico - Spanish Speaking Preferred

Fortrea
Fortrea
4+ years
$130,000 – $139,000
10 Jan. 6, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

FSP – Senior CRA II (Spanish-Speaking Preferred) – Midwest, Arizona, Texas, New Mexico

Location: Multiple Hub Locations in Midwest US, Arizona, Texas, New Mexico (Spanish fluency preferred; direct flight access to Puerto Rico a plus)
Job Type: Full-Time, Remote / Field-Based
Experience Required: 4+ years in on-site clinical monitoring
Job ID: 255287
Category: Clinical Research / FSP


About Fortrea

Fortrea is a global leader in clinical research, providing full-service outsourcing (FSP) solutions to top pharmaceutical, biotechnology, and medical device companies. Our mission is to accelerate clinical development through high-quality, compliant, and patient-focused research.

As part of our FSP Clinical Operations team, you will play a critical role in ensuring the success of IVD and therapeutic clinical trials while contributing to the advancement of patient care.


Position Overview

We are seeking Senior Clinical Research Associates (CRA II) fluent in Spanish for our Midwest, Arizona, Texas, and New Mexico hubs. This role requires extensive on-site monitoring experience, strong regulatory knowledge, and the ability to manage multiple clinical trial sites efficiently.


Key Responsibilities

  • Conduct all aspects of site monitoring including initiation, routine visits, and close-out activities.

  • Maintain accurate study files and ensure compliance with study protocols and regulatory requirements.

  • Verify informed consent procedures and protect participant safety in accordance with GCP and local regulations.

  • Ensure integrity of data entered in Case Report Forms (CRFs) and resolve data queries as per established guidelines.

  • Oversee registry management and perform feasibility work as required.

  • Complete Serious Adverse Event (SAE) reporting, narratives, and follow-up.

  • Conduct training and co-monitoring for new CRAs as needed.

  • Serve as Local Project Coordinator when assigned, liaising with sponsors, vendors, and study teams.

  • Provide input for process improvements and support continuous quality initiatives.


Required Qualifications

  • University or college degree, or certification in a related allied health profession (e.g., nursing, life sciences).

  • Minimum 4 years of on-site clinical monitoring experience across various therapeutic areas.

  • Experience in IVD or multi-therapeutic clinical trials preferred.

  • Proficiency with electronic data capture (EDC) systems and technology-based trial management.

  • Fluency in Spanish strongly preferred.

  • Excellent organizational, communication, and teamwork skills.

  • Ability to travel frequently (domestic and occasional international).


Work Environment

  • Primarily remote and field-based with frequent site visits.

  • Exposure to office and clinical site environments.

  • Physical requirements include sitting for extended periods, repetitive hand movements, occasional bending, lifting (up to 20 lbs), and travel flexibility.


Why Join Fortrea?

  • Competitive salary: $130,000 – $139,000 per year.

  • Comprehensive benefits package including Medical, Dental, Vision, Life, STD/LTD, 401(k), PTO, and employee recognition programs.

  • Opportunity to work with cutting-edge clinical trials across multiple therapeutic areas.

  • Flexible, remote-friendly environment with a focus on teamwork and innovation.