Clinical Research Assistant: Study Coordination & Data Support

UMass Med School; Worcester (MA); On-site; USD 36,000 - 40,000; Full time

Job summary

UMass Med School in Worcester, MA is seeking a Clinical Research Assistant to support human subjects research under the PI or designee. The role involves performing delegated tasks and ensuring data quality and protocol compliance for clinical studies.

You will assist in developing protocol-specific tools, collect and transport data and samples, schedule tests/interviews, conduct patient follow-up, maintain supplies, review records, and uphold patient confidentiality and study integrity.

Qualifications

• Bachelor's degree or equivalent experience.
• Experience using Microsoft Word, Excel, Access, Outlook, and PowerPoint.
• Strong oral and written communication skills.
• Excellent organizational and interpersonal skills.

Responsibilities

• Assist PI in development of protocol-specific tools to aid in study documentation.
• Collect, evaluate, update, and store/transport pertinent data and samples in relation to protocol.
• Schedule patient tests and/or interviews.
• Conduct patient telephone follow-up.
• Maintain operations including stock, inventory, store, and order samples/supplies.
• Review medical records and abstractions for consistency and completeness.
• Comply with policies, health and safety regulations and department objectives.
• Maintain patient and study subject confidentiality.

Skills

Oral or written communication skills

Excellent organizational skills

Interpersonal skills

Word

Excel

Access

Outlook

PowerPoint

Education

Bachelor's degree or equivalent experience

Tools

Word

Excel

Access

Outlook

PowerPoint

Job description

UMass Med School in Worcester, MA is seeking a Clinical Research Assistant to support human subjects research under the PI or designee. The role involves performing delegated tasks and ensuring data quality and protocol compliance for clinical studies.

You will assist in developing protocol-specific tools, collect and transport data and samples, schedule tests/interviews, conduct patient follow-up, maintain supplies, review records, and uphold patient confidentiality and study integrity.