Biomedical Ethics Coordinator - Research

Mayo Clinic • Rochester, MN

2d

About The Position

The biomedical ethics coordinator assists with multidisciplinary research
analysis using a variety of analytical, quantitative, and qualitative research
skills. The coordinator conducts comprehensive literature searches related to
biomedical ethics initiatives and compiles and summarizes written and electronic
data for research projects. Researches funding sources and collects necessary
documents for participating in external research collaborations. Writes draft
reports that clearly and concisely summarize and illustrate projects findings,
outcomes and results. Drafts sections of grants, abstracts and manuscripts.
Collects and assists in designing data analysis strategies, evaluating data
needs and methods of data collection. Implements the data collection protocol
including IRB submissions. Obtains consent and conducts interviews with study
participants. Assists in reviewing study methods. Evaluates the reliability of
data sources to ensure data integrity. Maintains and completes appropriate study
documents according to the study protocol, institutional policies, and
government regulations, if applicable. Determines which study documents are
appropriate and develops or creates additional documents as needed. Coordinates
multiple project assignments and is responsible for completing tasks in given
timeline. Designs and maintains quantitative and qualitative databases including
the management and updating of data.

Responsibilities

• Assists with multidisciplinary research analysis using a variety of analytical, quantitative, and qualitative research skills.
• Conducts comprehensive literature searches related to biomedical ethics initiatives.
• Compiles and summarizes written and electronic data for research projects.
• Researches funding sources and collects necessary documents for participating in external research collaborations.
• Writes draft reports that clearly and concisely summarize and illustrate projects findings, outcomes and results.
• Drafts sections of grants, abstracts and manuscripts.
• Collects and assists in designing data analysis strategies, evaluating data needs and methods of data collection.
• Implements the data collection protocol including IRB submissions.
• Obtains consent and conducts interviews with study participants.
• Assists in reviewing study methods.
• Evaluates the reliability of data sources to ensure data integrity.
• Maintains and completes appropriate study documents according to the study protocol, institutional policies, and government regulations, if applicable.
• Determines which study documents are appropriate and develops or creates additional documents as needed.
• Coordinates multiple project assignments and is responsible for completing tasks in given timeline.
• Designs and maintains quantitative and qualitative databases including the management and updating of data.

Benefits

• Medical: Multiple plan options.
• Dental: Delta Dental or reimbursement account for flexible coverage.
• Vision: Affordable plan with national network.
• Pre-Tax Savings: HSA and FSAs for eligible expenses.
• Retirement: Competitive retirement package to secure your future.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees