Clinical Research Assistant

UMass Med School; Worcester (MA); On-site; USD 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a Clinical Research Assistant to support clinical research protocols under the guidance of a Principal Investigator. This role involves developing tools for study documentation, collecting and managing data, and ensuring compliance with safety regulations. Ideal candidates will possess strong communication and organizational skills, along with a Bachelor's degree. Join a dynamic team dedicated to advancing medical research and making a meaningful impact in the field of healthcare.

Qualifications

• Bachelor's degree or equivalent experience required.
• Strong oral and written communication skills essential.
• Experience with computer tools like Word and Excel is necessary.

Responsibilities

• Assist in developing protocol-specific tools for study documentation.
• Collect and evaluate data and samples related to clinical protocols.
• Maintain patient confidentiality and ensure compliance with regulations.

Skills

Oral Communication

Written Communication

Organizational Skills

Interpersonal Skills

Education

Bachelor's Degree

Tools

Microsoft Word

Microsoft Excel

Microsoft Access

Microsoft Outlook

Microsoft PowerPoint

Job description

Clinical Research Assistant

Minimum Salary: US-MA-Worcester

Job Location: Worcester, MA

Requisition Number: 2025-47965

Number of Openings: 2

Posted Date: 4/28/2025 9:48 AM

Shift: Non Exempt

Exempt/Non-Exempt Status: Union Position-W28-SHARE

Overview

GENERAL SUMMARY OF POSITION:

Under the direction of the Principal Investigator or designee, the Clinical Research Assistant is responsible for performing delegated tasks and procedures involving human subjects in support of clinical research protocols.

Responsibilities

MAJOR RESPONSIBILITIES:

Clinical Operations

• 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 appropriate operations including stocking, inventory, storing, and ordering samples/supplies

Administration

• Review medical records and abstractions for consistency and completeness
• Ensure compliance with policies, safety regulations, and procedures
• Maintain patient and study subject confidentiality

Qualifications

REQUIRED QUALIFICATIONS:

• Bachelor's degree or equivalent experience
• Experience with computer tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
• Strong oral and written communication skills
• Excellent organizational and interpersonal skills