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 record 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 as needed including to stock inventory store and order samples/supplies
Administration
- 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
Qualifications
REQUIRED QUALIFICATIONS:
- Bachelors degree or equivalent experience
- Experience in using computer-based tools (Word Excel Access Outlook PowerPoint etc.)
- Oral and written communication skills
- Excellent organizational and interpersonal skills required
Additional Information
Added Qualifications:
- Meeting logistics agendas minutes and follow-ups
- Documentation systems (SOPs manuals of operations)
- Experience using project management tools to plan track and report on complex research and administrative workflows such as Microsoft Teams and Project/Planner
Required Experience:
Junior IC
OverviewGENERAL 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.ResponsibilitiesMAJOR RESPONSIBILITIES:Cl...
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 record 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 as needed including to stock inventory store and order samples/supplies
Administration
- 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
Qualifications
REQUIRED QUALIFICATIONS:
- Bachelors degree or equivalent experience
- Experience in using computer-based tools (Word Excel Access Outlook PowerPoint etc.)
- Oral and written communication skills
- Excellent organizational and interpersonal skills required
Additional Information
Added Qualifications:
- Meeting logistics agendas minutes and follow-ups
- Documentation systems (SOPs manuals of operations)
- Experience using project management tools to plan track and report on complex research and administrative workflows such as Microsoft Teams and Project/Planner
Required Experience:
Junior IC
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