CURRICULUM VITAE

 

Positions

University of North Carolina, Chapel Hill, North Carolina

2015-present  Associate Professor of Social Medicine, Center for Bioethics

2012-2015      Assistant Professor of Social Medicine, Center for Bioethics

 

Vanderbilt University, Nashville, Tennessee

2008-2012  Assistant Professor, Center for Biomedical Ethics & Society

 

Arizona State University, Tempe, Arizona

2005-2008  Assistant Professor, Women & Gender Studies Program

Faculty Affiliate, Consortium for Science, Policy & Outcomes

 

Education

Rensselaer Polytechnic Institute, Troy, New York

2005    Ph.D., with distinction, Science and Technology Studies

2002    M.S., Science and Technology Studies

 

Connecticut College, New London, Connecticut

1998    B.A., with honors, Psychology-Based Human Relations and French

 

Publications
Books

Fisher, Jill A. (In Press) Adverse Events: Race, Inequality, and the Testing of New Pharmaceuticals. New York, NY: New York University Press. Expected publication date: Spring 2020.

 

Fisher, Jill A. (Ed.) (2011) Gender and the Science of Difference: Cultural Politics of Contemporary Science and Medicine. New Brunswick, NJ: Rutgers University Press.

 

Fisher, Jill A. (2009) Medical Research for Hire: The Political Economy of Pharmaceutical Clinical Trials. New Brunswick, NJ: Rutgers University Press.

 

Special Issues of Academic Journals

Monahan, Torin & Jill A. Fisher (2008) Surveillance and Inequality. Surveillance & Society 5 (3).

 

Peer-Reviewed Articles

McManus, Lisa, Arlene Davis, Rebecca L. Forcier, and Jill A. Fisher (2019) "Appraising Harm in Phase I Trials: Healthy Volunteers’ Accounts of Adverse Events." Journal of Law, Medicine & Ethics 47 (2): 323-333.

 

Fisher, Jill A. & Rebecca L. Walker (2019) "Advancing Ethics and Policy for Healthy-Volunteer Research through a Model-Organism Framework." Ethics & Human Research 41 (1): 4-14.

 

Fisher, Jill A., Lisa McManus, Marci D. Cottingham, Julianne M. Kalbaugh, Megan M. Wood, Torin Monahan, & Rebecca L. Walker (2018) "Healthy Volunteers' Perceptions of Risk in U.S. Phase I Clinical Trials: A Mixed-Methods Study." PLOS Medicine 15 (11): e1002698.

 

Fisher, Jill A., Lisa McManus, Megan M. Wood, Marci D. Cottingham, Julianne M. Kalbaugh, Torin Monahan, & Rebecca L. Walker (2018) "Healthy Volunteers' Perceptions of the Benefits of their Participation in Phase I Clinical Trials." Journal of Empirical Research on Human Research Ethics 13 (5): 494-510.

 

Williams, Quintin & Jill A. Fisher (2018) "Captive to the Clinic: Phase I Clinical Trials as Temporal Total Institutions." Sociological Inquiry 88 (4): 724-748.

 

McManus, Lisa & Jill A. Fisher (2018) “To Report or Not to Report: Exploring Healthy Volunteers’ Rationales for Disclosing Adverse Events in Phase I Drug Trials.” AJOB Empirical Bioethics 9 (2): 82-90.

 

Walker, Rebecca L., Marci D. Cottingham, & Jill A. Fisher (2018) “Serial Participation and the Ethics of Phase 1 Healthy Volunteer Research.” Journal of Medicine and Philosophy 43 (1): 83-114.

 

Cottingham, Marci D., Julianne M. Kalbaugh, Teresa Swezey, & Jill A. Fisher (2018) “Exceptional Risk: Healthy Volunteers’ Perceptions of HIV/AIDS Clinical Trials.” Journal of Acquired Immune Deficiency Syndromes 79: S30-S36.
 

Henderson, Gail E., Holly L. Peay, Eugene Kroon, Rosemary Jean Cadigan, Karen Meagher, Thidarat Jupimai, Adam Gilbertson, Jill Fisher, Nuchanart Q. Ormsby, Nitiya Chomchey, Nittaya Phanuphak, Jintanat Ananworanich, Stuart Rennie (2018) “Ethics of Treatment Interruption Trials in HIV Cure Research: Addressing the Conundrum of Risk/Benefit Assessment.Journal of Medical Ethics 44 (4): 270-276.

 

Cottingham, Marci D. & Jill A. Fisher (2017) "From Fantasy to Reality: Managing Biomedical Risk Emotions in and through Fictional Media." Health, Risk & Society 19 (5-6): 284-300.

 

Fisher, Jill A. & Marci D. Cottingham (2017) "This Isn't Going to End Well: Fictional Representations of Medical Research in Television and Film." Public Understanding of Science 26 (5): 564-578.

 

Cottingham, Marci D. & Jill A. Fisher (2016) "Risk and Emotion Among Healthy Volunteers in Clinical Trials." Social Psychology Quarterly 79 (3): 222-242.

 

Monahan, Torin & Jill A. Fisher (2015) "‘I’m Still a Hustler’: Entrepreneurial Responses to Precarity by Participants in Phase I Clinical Trials.” Economy and Society 44 (4): 545-566.

 

Monahan, Torin & Jill A. Fisher (2015) “Strategies for Obtaining Access to Secretive or Guarded Organizations.” Journal of Contemporary Ethnography 44 (6): 709-736.

 

Edelblute, Heather B. & Jill A. Fisher (2015) “Using ‘Clinical Trial Diaries’ to Track Patterns of Participation for Serial Healthy Volunteers in U.S. Phase I Studies.” Journal of Empirical Research on Human Research Ethics 10 (1): 65-75.

 

Fisher, Jill A. (2015) “Feeding and Bleeding: The Institutional Banalization of Risk to Healthy Volunteers in Phase I Pharmaceutical Clinical Trials.” Science, Technology, & Human Values 40 (2): 199-226

 

Fisher, Jill A. (2015) “Stopped Hearts, Amputated Toes, and NASA: Contemporary Legends among Healthy Volunteers in US Phase I Clinical Trials.” Sociology of Health and Illness 37 (1): 127-142.

 

Cottingham, Marci D. & Jill A. Fisher (2015) "Consenting to Heteronormativity: Sexual Assumptions in Biomedical Research." About Gender 4 (7): 1-18.

 

Fisher, Jill A., Marci D. Cottingham, & Corey A. Kalbaugh (2015) "Peering into the Pharmaceutical 'Pipeline': Investigational Drugs, Clinical Trials, and Industry Priorities." Social Science & Medicine 131: 322-330.

 

Cottingham, Marci D., Corey A. Kalbaugh, & Jill A. Fisher (2014) “Tracking the Pharmaceutical Pipeline: Clinical Trials and Global Disease Burden.” Clinical and Translational Science 7 (4): 297-299.

 

Fisher, Jill A. (2013) “Expanding the Frame of ‘Voluntariness’ in Informed Consent: Structural Coercion and the Power of Social and Economic Context.” Kennedy Institute of Ethics Journal 23 (4): 355-379.

 

Fisher, Jill A. & Torin Monahan (2012) “Evaluation of Real-Time Location Systems in their Hospital Contexts.” International Journal of Medical Informatics 81 (10): 705-712.

 

Fisher, Jill A. & Corey A. Kalbaugh (2012) “United States Private-Sector Physicians and Pharmaceutical Contract Research: A Qualitative Study.” PLoS Medicine 9 (7): e1001271.

 

Fisher, Jill A. & Corey A. Kalbaugh (2012) “Altruism in Clinical Research: Coordinators’ Orientation to their Professional Roles.” Nursing Outlook 60 (3): 143-148.

 

Fisher, Jill A. & Corey A. Kalbaugh (2011) “Challenging Assumptions About Minority Participation in U.S. Clinical Research.” American Journal of Public Health 101 (12): 2217-2222.

 

Monahan, Torin & Jill A. Fisher (2011) “Surveillance Impediments: Recognizing Obduracy with the Deployment of Hospital Information Systems.” Surveillance & Society 9 (1/2): 1-16.

 

Fisher, Jill A. & Torin Monahan (2011) “The ‘Biosecuritization’ of Healthcare Delivery: Examples of Post-9/11 Technological Imperatives.” Social Science & Medicine 72 (4): 545-552.

 

Monahan, Torin & Jill A. Fisher (2010) “Implanting Inequality: Empirical Evidence of Social and Ethical Risks of Radio-Frequency Identification (RFID) Devices.” International Journal of Technology Assessment in Health Care 26 (4): 370-376.

 

Fisher, Jill A. & Lorna M. Ronald (2010) “Sex, Gender, and Pharmaceutical Politics: From Drug Development to Marketing.” Gender Medicine 7 (4): 357-370.

 

Monahan, Torin & Jill A. Fisher (2010) “Benefits of ‘Observer Effects’: Lessons from the Field.” Qualitative Research 10 (3): 357–376.

 

Fisher, Jill A. (2010) “Re-inscribing Gender within New Modes of Medical Expertise: The Investigator-Coordinator Relationship in the Clinical Trials Industry.” Gender, Work & Organization 17 (2): 150-173.

 

Fisher, Jill A. (2008) “Institutional Mistrust in the Organization of Pharmaceutical Clinical Trials.” Medicine, Health Care, and Philosophy 11 (4): 403-13.

 

Fisher, Jill A. (2008) “Practicing Research Ethics: Private-Sector Physicians & Pharmaceutical Clinical Trials.” Social Science & Medicine 66 (12): 2495-2505.

 

Fisher, Jill A. & Torin Monahan (2008) “Tracking the Social Dimensions of RFID Systems in Hospitals.” International Journal of Medical Informatics 77 (3): 176-183.

 

Fisher, Jill A. (2007) “‘Ready-to-Recruit’ or ‘Ready-to-Consent’ Populations?: Informed Consent and the Limits of Subject Autonomy.” Qualitative Inquiry 13 (6): 875-894.

 

Fisher, Jill A. (2007) “Coming Soon to a Physician Near You: Medical Neoliberalism and Pharmaceutical Clinical Trials.” Harvard Health Policy Review 8 (1): 61-70.   

 

Fisher, Jill A. (2007) “Governing Human Subjects Research: Individualized Ethics and Structural Inequalities.” Science & Public Policy 34 (2): 117-126.

 

Fisher, Jill A. (2006) “Co-ordinating ‘Ethical’ Clinical Trials: The Role of Research Coordinators in the Contract Research Industry.” Sociology of Health and Illness 28 (6): 678-694.

 

Fisher, Jill A. (2006) “Procedural Misconceptions and Informed Consent: Insights from Empirical Research on the Clinical Trials Industry.” Kennedy Institute of Ethics Journal 16 (3): 251-268.

 

Fisher, Jill A. (2006) “Playing Patient, Playing Doctor: Munchausen Syndrome, Clinical S/M, and Ruptures of Medical Power.” Journal of Medical Humanities 27 (3): 135-149.

 

Fisher, Jill A. (2006) “Investigating the Barons: Narrative & Nomenclature in Munchausen Syndrome.” Perspectives in Biology and Medicine 49 (2): 250-262.

 

Fisher, Jill A. (2002) “Tattooing the Body, Marking Culture.” Body & Society 8 (4): 91-107.

 

Book Chapters  

Fisher, Jill A. (2011) “Gendering Science: Contextualizing Historical and Contemporary Pursuits of Difference.” In J.A. Fisher (Ed.), Gender and the Science of Difference: Cultural Politics of Contemporary Science and Medicine (pp. 1-23). New Brunswick, NJ: Rutgers University Press.

 

Fisher, Jill A. & Lorna M. Ronald (2008) “Direct-to-Consumer Responsibility: Medical Neoliberalism in Pharmaceutical Advertising and Drug Development.” In S.M. Chambré & M. Goldner (Eds.), Patients, Consumers and Civil Society (Advances in Medical Sociology, Volume 10) (pp. 29-51). Brighton, UK: Emerald Publishing.

 

Fisher, Jill A. (2006) “Indoor Positioning and Digital Management: Emerging Surveillance Regimes in Healthcare.” In T. Monahan (Ed), Surveillance and Security: Technological Politics and Power in Everyday Life (pp. 77-88). New York: Routledge.

 

Comparative Effectiveness Reports

Lindegren ML, Krishnaswami S, Fonnesbeck C, Reimschisel T, Fisher J, Jackson K, Shields T, Sathe NA, McPheeters ML. Adjuvant Treatment for Phenylketonuria (PKU). Comparative Effectiveness Review No. 56. (Prepared by the Vanderbilt Evidence-based Practice Center under Contract No. HHSA 290-2007-10065-I.) AHRQ Publication No. 12- EHC035-EF. Rockville, MD: Agency for Healthcare Research and Quality. February 2012.

 

Walsh WF, Chescheir NC, Gillam-Krakauer M, McPheeters ML, McKoy JN, Jerome R, Fisher JA, Meints L, Hartmann, KE. Maternal-Fetal Surgical Procedures. Technical Brief No. 5. (Prepared by the Vanderbilt Evidence-based Practice Center under Contract No. 290-2007-10065.) AHRQ Publication No. 10(11)-EHC059-EF. Rockville, MD: Agency for Healthcare Research and Quality. April 2011.

 

Hartmann KE, McPheeters ML, Biller DH, Ward RM, McKoy JN, Jerome RN, Micucci SR, Meints L, Fisher JA, Scott T, Slaughter JC, Blume JD (2009) Treatment of Overactive Bladder in Women. Evidence Report/Technology Assessment No. 187 (Prepared by the Vanderbilt Evidence-based Practice Center under Contract No. 290-2007-10065-I.) AHRQ Publication No. 09-E017. Rockville, MD: Agency for Healthcare Research and Quality. August 2009.

 

Grants
PI or Co-PI

2017-2021  "Healthy Volunteers as Model Organisms: Comparative Research Ethics and Policy for Phase I Trials" National Institutes of Health, Principal Investigator [with Rebecca L. Walker (Co-PI)], $1,586,100.

  • 2018-2019 Awarded R01 Administrative Supplement for Research on Sex/Gender Influences, $101,075

 

2012-2017  “Factors Affecting Healthy Volunteers’ Long-Term Participation in Clinical Trials” National Institutes of Health, Principal Investigator, $1,874,216.

  • 2016-2017 Awarded R01 Administrative Supplement, $60,800

  • 2013-2014 Awarded Research Supplement to Promote Diversity in Health-Related Research, $38,451.

 

2009-2012  “Phase I Clinical Trials and the Informed Consent of Healthy Subjects" National Institutes of Health, Principal Investigator, $385,058.

 

2007-2010  “Effects of RFID Technologies on Organizational Dynamics in Hospitals” National Science Foundation, Principal Investigator [with Torin Monahan (Co-PI)] $247,162.

 

2006-2009  “Workshops on Surveillance and Society” National Science Foundation, Co-Principal Investigator [with Torin Monahan (PI), Gary Marx (Co-PI), & Simon Cole (Co-PI)], $108,807.

 

2003-2005  “Informed Consent in Private Sector Mental Health Research” Kirschstein-National Research Service Award, National Institute of Mental Health (NIH), Principal Investigator, $82,503

 

Co-Investigator or Collaborator

2016-2020 “Integrating Decision Making Studies into HIV Cure Trials: A Real-Time Longitudinal Assessment” (PI: Gail Henderson). National Institute of Allergy and Infectious Disease (NIH), Co-Investigator, $2,200,000 (estimate ).

 

2013-2018 “North Carolina Translational & Clinical Sciences Institute (NC TraCS)” (PI: Marschall Runge). National Center for Advancing Translational Sciences, NIH Clinical and Translational Science Awards (CTSA), Co-Investigator (Clinical Research Ethics Resource – Leader, Ethics of Commercialization Initiative), $54,600,000 (estimate).

 

2009-2012  “American Recovery and Reinvestment Act of 2009: Comprehensive EPC Comparative Effectiveness Reviews for Effective Health Care” (PI: Katherine Hartmann). Agency for Healthcare Research and Quality (AHRQ), Co-Investigator, $3,000,000.

 

2007-2012 “The Vanderbilt Institute for Clinical and Translational Research (VICTR)” (PI: Gordon Bernard). National Center for Research Resources, NIH Clinical and Translational Science Awards (CTSA), Co-Investigator (added to project in Fall 2011), $45,689,350.

 

Awards & Honors

2010  Medical Research for Hire selected for Author Meets Critics Session at the American Sociological Association Conference held in Atlanta, GA, August 2010.

 

2004  Selected as a recipient of the Founders Award of Excellence for recognition of academic achievement and campus leadership at Rensselaer Polytechnic Institute.

 

2003-2004  Awarded a graduate scholarship from Delta of Connecticut Chapter of Phi Beta Kappa for dissertation research.

 

2002  Awarded level of distinction on Science Studies Field Examination as part of the doctoral requirements in Science & Technology Studies at Rensselaer Polytechnic Institute, Summer 2002.

 

1998  Awarded the Jane W. Torrey Prize for the study of social issues at Connecticut College, April 1998.

 

1998  Awarded the Esther Cary Prize for excellence in French at Connecticut College, April 1998.

 

1998  Inducted into Phi Beta Kappa, the National Honor Society for undergraduates, at Connecticut College, May 1998.

 

1997  Awarded the Nelly K. Murstein Prize for achievement in French at Connecticut College, April 1997.

 

Service to the Profession

 

2014-2015  Chair of the Hacker-Mullins Student Paper Award Committee, American Sociological Association.

 

2013-2014  Chair of the Robert K. Merton Book Award Committee, American Sociological Association.

 

2012-    “Bioethics (Re)Considered” Section Editor for Cambridge Quarterly of Healthcare Ethics.

 

2012-2013  Member of the Star-Nelkin Award Committee, American Sociological Association.

 

2012-2015  Elected as Council Member to the Section on Science, Knowledge and Technology, American Sociological Association.

 

2011  Advisory Panel member for the National Science Foundation.

 

2007  Member of the program committee for the 2007 Annual Meeting of the Society for Social Studies of Science

The University of North Carolina at Chapel Hill