Clinical Research Office Coordinator — Scheduling & Support

Adams Clinical, Inc.

Dallas (TX)

On-site

USD 26,000 - 32,000

Full time

4 days ago
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Benefits offered by this job

401(k) matching
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave

Job summary

Adams Clinical, Inc. seeks a Clinical Research Office Coordinator to support day-to-day operations at our Dallas site. You will handle participant support, scheduling, and office management, serving as a liaison among clinicians, coordinators, assistants, and participants.

Responsibilities include reminders, transportation coordination, portal updates, and cross-site scheduling. The role emphasizes organization, communication, and a welcoming environment within a regulated research setting.

Qualifications

  • Strong organizational skills and attention to detail.
  • Excellent written and verbal communication, including phone etiquette.
  • Customer service and interpersonal skills in a professional environment.
  • Proficiency with Microsoft Office Suite in a regulated clinical setting.
  • Ability to stand, walk, and lift/move study supplies as needed.

Responsibilities

  • Greet and support participants, manage reminders, and assist with transportation and meals.
  • Coordinate scheduling across clinicians and study staff; relay updates to CRAC team.
  • Open, prepare, and maintain a welcoming office space; manage supplies and events.
  • Support study teams with materials prep, informed consent, assessments, and payments.

Skills

Organizational skills
Communication skills
Customer service
Microsoft Office
Professional phone/email etiquette
Regulatory data handling
Multitasking

Tools

Microsoft Office Suite

Job description

Adams Clinical, Inc. seeks a Clinical Research Office Coordinator to support day-to-day operations at our Dallas site. You will handle participant support, scheduling, and office management, serving as a liaison among clinicians, coordinators, assistants, and participants.

Responsibilities include reminders, transportation coordination, portal updates, and cross-site scheduling. The role emphasizes organization, communication, and a welcoming environment within a regulated research setting.

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