Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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Job Information

MNGI Digestive Health, P.A. Clinical Research Coordinator in Plymouth, Minnesota

Description Job Purpose: The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI) and Research Department Director. The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works closely with the PI, Department Director, Sponsor, and Clinical Research Organization (CRO) to support and provide guidance on the administration of all related aspects of the clinical study. This position is based at our Plymouth location, with regular travel to our clinic locations in Northeast Minneapolis and Maplewood. Essential Functions: In order to perform this job successfully, an individual must be able to perform each essential function satisfactorily and regular attendance is required. The responsibilities listed below are representative of the primary essential functions required; additional duties may be assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. General Administration: Coordinate with PI and Department Director to ensure that clinical research and related activities are performed in accordance with Federal regulations, GCP, MNGI policies and procedures, and sponsoring agency policies and procedures. Assist the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, and execution of research plan. Maintain documentation of training. Assist PI to assure that all key personnel or persons engaged in the research project have met training requirements in accordance with Federal regulations and sponsoring agency policies and procedures. Coordinate and facilitate monitoring and auditing visits. Notify appropriate organizational and sponsor agency officials of external audits by FDA and sponsors. Collaborate with PI and institution to respond to any audit findings and implement approved recommendations. Budget: Collaborate with the Department Director and Research Finance personnel to prepare a preliminary categorized budget and justification. Confirm accuracy and completeness of budgeted costs. Protocol Preparation and Review: Review and comprehend the protocol. Attend investigator meetings as required or requested by the sponsoring agency. Prepare other study materials as requested by the sponsor. These study materials include, but are not limited to, the informed consent document, case report forms (CRFs), enrollment logs, and drug/device accountability logs. Prepare applicable submission forms and submits updated documents Create training materials for research PIs, Sub-Is and staff and facilitate documentation of training completion. Establish and organize study files, including but not limited to the study specific source documentation, the regulatory binders and other materials. Conduct of Research Review and develop a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections. Assist PI in communication of study requirements to all individuals involved in the study. Provide appropriate training and tools for study team members. Document date of training and signatures of study personnel trained on study specific training log. Work with the PI to develop and implement recruitment strategies in accordance with IRB requirements and approvals. Conduct and participate in the informed consent process including interactions with research participants, answering any questions related to the study. Obtain appropriate signatures and dates on forms in appropriate places. Assure that amended consent forms are appropriately implemented and signed. Scr