A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.

Responsible for operation of a specialized breast cancer research laboratory with one or more faculty members within a department and/or works in specialized research area. May act as liaison with other departments, divisions or organizations. Develops, designs and conducts one or more small or moderately complex research experiments in line with plan, reviews progress and evaluates results. Formulates research methods and suggests options for improving quality, identifies potential problems, recommends and implements solutions, and collaborates in the development of new techniques. Trains users and students in equipment operation and laboratory techniques, explains and demonstrates technology and equipment capabilities, operations, limitations and outcomes. Coordinates data collection and screening and verifies the data. Conducts analysis of data, interprets and implements research methodology based on outcome of analysis. Co-authors publications and may co-present results with Principal Investigator at meetings and/or conferences. Has oversight for day-to-day operation of laboratory and may supervise exempt and non-exempt research and support personnel. 

General Responsibilities/Skills: 

1. Developed and maintained translational research study records, sample inventories, and regulatory documents (5%).
2. Created laboratory and study budgets, databases, detailed standard operating procedures (5%).
3. Established and implemented training on standard operating procedures and laboratory safety for new team members (5%).
4. Managed laboratory and department administrative tasks such as report preparation, supply inventory, hiring, and safety inspections (5%).
5. Created and maintained IRB applications, renewals, amendments, deviations, protocol and informed consent documents for multiple human research studies using eResearch (10%).
6. Extracted relevant clinical data from study participants using MiChart and EMERSE to create detailed databases, identify eligible patients for study recruitment, and coordinate longitudinal specimen collection across several concurrent studies (10%).
7. Obtained informed consent and collected blood samples following standard venipuncture technique from healthy study participants (10%).
8. Processed, analyzed, and banked human blood and cerebrospinal fluid samples from multi-institutional clinical trials for translational research (10%)
9. Cultured human cancer cell lines using sterile techniques (5%).
10. Performed next generation sequencing of ctDNA and FFPE tissue samples (5%).
11. Communicated with collaborators from within UM and outside industry partners/sponsors to coordinate multiple, concurrent project details, update study documentation and laboratory certifications, and quality check and prepare data for analysis (10%).
12. Prepared preliminary data for presentation at internal laboratory meetings, national conferences, and incorporation into grant applications (10%).
13. Contributed to laboratory publications including data analysis, table and figure preparation, manuscript writing and editing, and manuscript submission (10%).

Education and Experience: 

• Bachelor's or Master's degree in a recognized field of science or learning which is directly related to the duties of the position and 4 to 5 years related experience.

• Supervisory and financial management experience preferred.

   

Over 5 years of basic and clinical translational breast cancer research including extensive knowledge in laboratory techniques and clinical human research regulatory policies.

Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems.  In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.

What Benefits can you Look Forward to?

• Excellent medical, dental and vision coverage effective on your very first day
• 2:1 Match on retirement savings

Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.

This position is 40 hours / week split between the lab and breast cancer clinic. 

Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings.  Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.

Job openings are posted for a minimum of seven calendar days.  The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.

The University of Michigan is an equal employment opportunity employer.