Biomedical Ethics Coordinator - Research

Mayo Clinic•Rochester, MN

60d

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.

Requirements

Variety of analytical, quantitative, and qualitative research skills.
Ability to conduct comprehensive literature searches.
Ability to compile and summarize data.
Ability to research funding sources.
Ability to write draft reports.
Ability to draft sections of grants, abstracts and manuscripts.
Ability to collect and assist in designing data analysis strategies.
Ability to evaluate data needs and methods of data collection.
Ability to implement data collection protocols, including IRB submissions.
Ability to obtain consent and conduct interviews.
Ability to review study methods.
Ability to evaluate the reliability of data sources.
Ability to maintain and complete study documents according to protocol, institutional policies, and government regulations.
Ability to determine appropriate study documents and create additional documents as needed.
Ability to coordinate multiple project assignments and complete tasks within a given timeline.
Ability to design and maintain quantitative and qualitative databases.

Responsibilities

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.