We are looking to hire an experienced Research project specialist to join our talented team at University of Minnesota in Minneapolis, MN.
Growing your career as a Full Time Research project specialist is an unparalleled opportunity to develop excellent skills.
If you are strong in analysis, adaptability and have the right attitude for the job, then apply for the position of Research project specialist at University of Minnesota today!
Full job description Required Qualifications:
Requires BA/BS with at least 8 years of experience or Advanced degree in related field with at least 6 years professional experience Knowledge of clinical research compliance standards, e.g. informed consent process, adverse event reporting, the Federal Code of Regulations and Good Clinical Practices (GCP) Standards Prior experience working with The Institute on the Biology of Aging and Metabolism
Preferred Qualifications:
Master's degree in Clinical Research Demonstrated data management skills, such as data collection, data entry and quality control Detail-oriented with strong organizational, planning and problem-solving skills Responsibilities:
Scientific Communications & Consulting (80%):
Communication liaison and primary contact between iBAM and the study PIs, clinicians and study staff. Primary contact for the University core facilities involved in clinical studies (UMGC, Bionet, TTL, CRL). Responsible for creating and updating study protocols and addressing any study related issues with core facilities and testing. Provides ongoing in-depth analysis and scientific input into development and execution of protocols and clinical development plans Remains current on issues in scientific expertise through active, ongoing participation in relevant scientific meetings, courses and literature review Works with the medical/scientific/regulatory team to creatively solve a wide range of medical/scientific/clinical/regulatory problems Provides writing, review, editing and QC of applicable project documents, including: IRBs, grant proposals, reports, protocols, amendments, informed consent forms, manuscripts, clinical development plans and analysis plans that meet scientific and regulatory standards, as necessary Provides scientific and logistical rationale/input for including assays or biomarkers for proof-of-concept studies or endpoint determination. Possibly involved in initial protocol development and optimization Supports training in key scientific and technical areas Supports the review and interpretation of data from clinical studies, including data files, tables, figures and listings Participates in and/or leads process improvement initiatives such as establishing and improving document standards, documentation processes, developing new procedures, process mapping and SOP review/revision Operations & Finance (20%)
Creates, manages, or participates in clinical study timelines and budgets Manages human tissue repository Maintains protocols and SOPs for clinical studies Manages sample transfer and tracking between cores and/or study personnel Applications must be submitted online. To be considered for this position, please click the Apply button and follow the instructions. You will be given the opportunity to complete an online application for the position and attach a cover letter and resume.
Additional documents may be attached after application by accessing your "My Job Applications" page and uploading documents in the "My Cover Letters and Attachments" section.
To request an accommodation during the application process, please e-mail View email address on jobs.institutedata.com or call (612) 624-UOHR (8647).
The University recognizes and values the importance of diversity and inclusion in enriching the employment experience of its employees and in supporting the academic mission. The University is committed to attracting and retaining employees with varying identities and backgrounds.
The University of Minnesota provides equal access to and opportunity in its programs, facilities, and employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression. To learn more about diversity at the U:
Any offer of employment is contingent upon the successful completion of a background check. Our presumption is that prospective employees are eligible to work here. Criminal convictions do not automatically disqualify finalists from employment.
The University of Minnesota, Twin Cities (UMTC)
The University of Minnesota, Twin Cities (UMTC), is among the largest public research universities in the country, offering undergraduate, graduate, and professional students a multitude of opportunities for study and research. Located at the heart of one of the nation's most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.
Benefits of working as a Research project specialist in Minneapolis, MN:
? Career Growth Potential
? Rapid Progression
? Competitive salary
