Clinical Research Coordinator

AECOM; United States; Remote; USD 50,000 - 75,000; Full time

Benefits offered by this job

Full-time

Remote position

U.S.-based applicants

Job summary

AECOM seeks a detail-oriented Clinical Research Coordinator to support clinical research activities, coordinate study operations, maintain documentation, and ensure compliance with guidelines and protocols.

The ideal candidate will have strong organizational and communication skills, experience with data collection and documentation, and the ability to work independently in a remote environment while coordinating with multidisciplinary teams.

Responsibilities

• Coordinate and support day-to-day clinical research activities.
• Assist with clinical study planning, execution, and monitoring.
• Maintain accurate research records, databases, and documentation.
• Coordinate with researchers, healthcare professionals, and study participants.
• Ensure compliance with study protocols and applicable regulatory requirements.
• Track study progress, prepare reports, and manage research-related documentation.
• Support data collection, review, and quality checks.
• Assist with scheduling and coordinating research-related activities.

Skills

Clinical research processes

Communication skills

Organizational skills

Data management

Attention to detail

Independent remote work

Tools

Microsoft Office

Research databases

Job description

AECOM is seeking a detail-oriented Clinical Research Coordinator to support clinical research activities, coordinate study operations, maintain research documentation, and ensure compliance with applicable clinical research guidelines and protocols. The ideal candidate should have strong organizational, communication, documentation, and coordination skills, along with an understanding of clinical research processes.

Responsibilities

• Coordinate and support day-to-day clinical research activities.
• Assist with clinical study planning, execution, and monitoring.
• Maintain accurate research records, databases, and documentation.
• Coordinate with researchers, healthcare professionals, and study participants.
• Ensure compliance with study protocols and applicable regulatory requirements.
• Track study progress, prepare reports, and manage research-related documentation.
• Support data collection, review, and quality checks.
• Assist with scheduling and coordinating research-related activities.

Qualifications

Not specified.

Required Skills

• Knowledge of clinical research processes and procedures.
• Strong communication and organizational skills.
• Data management and documentation skills.
• Attention to detail and problem-solving abilities.
• Ability to work independently in a remote environment.
• Proficiency in Microsoft Office and relevant research tools.

Preferred Skills

Not specified.

Pay range and compensation package

Not specified.

Equal Opportunity Statement

Not specified.

• Full-time opportunity
• Remote position
• U.S.-based applicants

Work Authorization

• Candidates with valid U.S. work authorization may apply:
• OPT
• STEM OPT
• Green Card (GC)
• H-1B