Clinical Research Manager – Clinical Trials Operations
Job ID: R-01332713
Employment Type: Full-Time
Work Mode: Fully Onsite
Location: Austin, Texas, United States
Category: Clinical Research | Clinical Trial Management | CRO Operations
Experience Required: Minimum 2–5 years in clinical research operations
About the Organization
Our Clinical Research Services team is at the forefront of advancing innovative therapies that address some of the world’s most pressing health challenges. As part of a globally leading Contract Research Organization (CRO), the team supports the PPD® clinical research portfolio and delivers high-quality clinical trials across inpatient and outpatient settings.
With clinical trials conducted in over 100 countries, the organization combines laboratory, digital, and decentralized clinical trial capabilities to accelerate the development of life-changing therapies. Employees are empowered with the resources, technology, and support needed to deliver accurate, compliant, and impactful research outcomes.
Role Overview
The Clinical Research Manager is responsible for managing all operational aspects of assigned clinical trials involving both healthy volunteers and patient populations. This role serves as a critical liaison between project management, investigators, clinical research teams, and external stakeholders, ensuring seamless communication, regulatory compliance, and high-quality trial execution.
The position plays a key role in aligning study operations with client expectations, regulatory requirements, and internal performance standards.
Key Responsibilities
Clinical Trial Management
Manage end-to-end operational activities for assigned clinical trials in inpatient and outpatient settings
Ensure clinical studies are conducted in compliance with FDA regulations, ICH-GCP guidelines, and internal SOPs
Oversee study execution, timelines, and deliverables to meet protocol and client requirements
Cross-Functional & Client Coordination
Act as the primary liaison between project managers, investigators, research teams, and clients
Communicate client requirements and protocol specifications clearly to clinical research teams
Escalate study-related issues, risks, and questions to project leadership and clients for timely resolution
Operational Oversight & Planning
Support study budgeting, forecasting, and operational planning activities
Monitor study progress and adapt operational plans to meet evolving study needs
Ensure accurate documentation and reporting throughout the study lifecycle
Education & Experience Requirements
Required Qualifications
Bachelor’s degree or equivalent in a scientific, healthcare, or related discipline
Minimum 2+ years of relevant clinical research experience, preferably within a CRO or clinical trial environment
Strong working knowledge of Phase I clinical trial processes and clinical study operations
Demonstrated understanding of FDA regulations and ICH-GCP guidelines
Preferred Experience
Experience managing clinical trials involving both healthy volunteers and patient populations
Exposure to budgeting, forecasting, and project planning in clinical research settings
Key Skills & Competencies
Strong organizational and prioritization skills with the ability to adapt to changing study requirements
Excellent written and verbal communication skills
Effective time management and multi-tasking abilities
Consulting mindset with the ability to collaborate across internal and external teams
Proficiency in Microsoft Office applications and clinical trial management systems
Attention to detail with a strong commitment to data quality and regulatory compliance
Work Environment
Fully onsite role based in Austin, Texas
Office and clinical research environment
Use of personal protective equipment (PPE) as required, including protective eyewear, gowning, gloves, and lab coats
Schedule may vary based on study requirements
Why Join This Opportunity?
This role offers the opportunity to work within a globally respected CRO, contributing directly to the execution of high-impact clinical trials. You will collaborate with cross-functional experts, gain exposure to diverse clinical research models, and play a meaningful role in advancing therapies that improve patient outcomes worldwide.
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