Senior Implementation Research Coordinator

* Manages all aspects of conducting research including: protocol development for the following tasks: screening, enrollment, subject follow-up, completion of the case report form, and adverse event reports.
* Coordinate the conduct of the study from startup through closeout.
* Educates community members about study procedures to be performed, visit schedule, what to report between and during visits, and the risks and benefits of the procedures.
* Performs assessments at visits and monitors for adverse events.
* Organizes and attends site visits from sponsors and other relevant study meetings.
* Supports recruitment and oversight of community advisory board for relevant projects.
* Protect community members and data confidentiality by ensuring security of research data and personal health information and compliance with federal regulations and sponsor protocols.
* Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), and study related communication.
* Understand the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and timely preparation of IRB submissions independently.
* Ensure compliance with federal regulations and institutional policies.
* May prepare and maintain protocol submissions and revisions.
* Performs for all tasks in complex clinical studies.
* Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
* Performs other related work as needed.
* Clinical or public health research experience.
* Experience coordinating multiple studies (e.g., investigator initiated, multi-site trials).
* Demonstrated effective leadership and teaching skills.
* Strong organizational skills.
* Strong knowledge of program subject matter.
* Strong interpersonal skills and the ability to work both independently and as part of a team.
* Flexibility.
* Creativity.
* Ability to manage stressful situations.
* Ability to maintain confidentiality.
* Ability to work on multiple projects simultaneously, set priorities, and meet deadlines.
* Ability and/or willingness to provide HIV/STI treatment, education, and prevention in nontraditional settings (community venues).
* Proficiency in the use of Microsoft Applications, including but not limited to Outlook, Excel, and Word.
* Demonstrated written and verbal communication skills and strong analytical skills.
* Proficiency in both qualitative and quantitative research.
* Ability to work on multiple projects.
* Ability to adapt to dynamic clinical environments such as the emergency department and work with flexible schedules.

When applying, the document(s)
** MUST
* * be uploaded via the
** My Experience
** page, in the section titled
** Application Documents
** of the application.

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