Clinical Research Assistant II

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* Assist with recruitment and enrollment of study participants.
* Administer phone screens and assess potential participants’ eligibility for inclusion in the study via screening forms and checklists.
* Collect in-person informed consent and oversee enrollment process that follows.
* Interact with participants prior to enrollment and maintain communication/compliance throughout study life-cycle.
* Actively participate in data collection, including administering questionnaires and collecting biological samples and physiological data.
* Develop and pilot-test data collection forms and procedures (hardcopy and/or electronic databases, etc.)
* Directly respond to inquiries regarding study protocol and policy. Serve as liaison or point-person for the study.
* Communicate with the PI concerning appropriate issues during interaction with participants.
* Plan agendas and provide logistical support for meetings with study teams.
* Collaborate on manuscripts for peer-reviewed journals, including co-authorship of papers.
* Participate in decisions made for the study and formulation of study-specific policies and procedures. Identify modifications needed and work to implement solutions.
* Performs all other duties, as assigned.
* Ability to work well in a team, as well as independently.
* Ability to organize and prioritize multiple tasks, and set deadlines.
* Excellent interpersonal, oral, and written communication skills.
* Careful attention to detail.
* Computer literacy and word processing skills.
* Ability to demonstrate professionalism and respect for subjects rights and individual needs.
* Ability to manage and maintain accurate records across several ongoing projects.
* Comfort with technology and ability to learn new research tools and devices; all necessary training will be provided.

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