Clinical Research Coordinator Job at Pragmatic, San Antonio, TX

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  • Pragmatic
  • San Antonio, TX

Job Description

Clinical Research Coordinator

San Antonio, TX | On-Site | Growth Opportunity

A growing outpatient clinical research organization is building a national network focused on FDA-regulated device studies (IDE and post-market). Partnering directly with physician-led practices, this group is bringing innovative clinical research into the outpatient setting.

We are seeking a Clinical Research Coordinator (CRC) in San Antonio who is looking for more than a task-driven role — someone who takes ownership, operates independently, and wants to grow as the organization expands.

This position is embedded within a physician’s outpatient practice and requires strong on-site engagement to ensure study success.

What Makes This Opportunity Different

• Direct exposure to FDA-regulated device trials (IDE and post-market)

• Real autonomy in managing study operations

• Close collaboration with physicians in a procedural outpatient setting

• Performance-based enrollment bonus

• Clear pathway to Senior CRC progression as the organization grows

This is a scaling environment where initiative, accountability, and reliability matter.

What You’ll Be Responsible For

• Screening and enrolling study participants

• Conducting and documenting informed consent per ICH-GCP standards

• Coordinating study visits and patient follow-up

• Maintaining audit-ready regulatory documentation

• Managing data entry and query resolution in EDC systems

• Preparing for sponsor monitoring visits

• Building productive working relationships with physicians and clinic staff

What Success Looks Like

• Consistent and professional on-site presence

• Proactive management of study timelines and visit windows

• Clear, early communication when issues arise

• Strong relationships with physicians and clinical staff

• High level of organization and attention to detail

What We’re Looking For

• 2+ years of clinical research experience (device experience preferred, not required)

• Working knowledge of ICH-GCP and FDA regulations

• Strong organizational and time management skills

• Confidence interacting directly with physicians

• Independent, ownership-driven mindset

Healthcare professionals transitioning into research are encouraged to apply.

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