SEARCH CAREER OPPORTUNITIES

GENERAL SUMMARY OF POSITION: 

Under the supervision 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. ** This is a per diem position, up to 19 hrs**

MAJOR RESPONSIBILITIES:

• Assist PI in development of protocol-specific tools to aid in study documentation
• Assess eligibility of research subjects in accordance with the approved protocol and all applicable regulations including HIPAA
• Obtain patient consent and Human Subject Committee approvals for minimal-risk studies as delegated by IRB-approved protocol
• Collect, record, evaluate, update, and store/transport pertinent data and samples in relation to protocol
• Track study enrollment and completion of milestones
• Summarize research findings and prepare presentations
• Perform literature searches
• Schedule patient tests and/or interviews
• Conduct patient telephone follow up
• Stock, inventory, store, and order samples/supplies as needed to maintain appropriate operations
• Review medical records and medical record abstractions for consistency and completeness
• Comply with established policies, health and safety regulations and requirements, procedures, and department objectives
• Maintain patient and study subject confidentiality
• Perform other duties as required.

REQUIRED QUALIFICATIONS:

• Bachelors degree in a scientific or health care field, or related experience
• Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
• Oral and written communication skills
• Excellent organizational and interpersonal skills required.

Applicants must be comfortable approaching patients in the ED and acute care setting.

PREFERRED QUALIFICATIONS:

• Experience in healthcare setting, either clinical or research

• The applicant will be working on multiple projects so flexibility is a must
• Off-site travel may be required within the Worcester area