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Clinical Research Associate Resume Example

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CLINICAL RESEARCH ASSOCIATE
Professional Overview

High performing, strategic thinking professional with more than eight years' experience in clinical research in the industry, nonprofit and higher education sectors. Highly skilled at relationship building with clinical research collaborations across departments and teams; exceptional writing, presenting, and interpersonal communication skills. Adept at assessing needs, generating options, and implementing solutions in collaboration with pharmaceutical, medical device and internal clients and stakeholders. Well versed in all phases of clinical research, including defining departmental and patient needs, assessing

needed resources and evaluating successful study initiation outcomes. Experienced at managing projects from the start-up and study initiation through to completion and study close out.

Core Qualifications
  • Internal Medicine
  • Public Health
  • Cardiovascular
  • Neurosurgery
  • Goal setting and implementation
  • Grant writing
  • Program Development
  • Team building
Accomplishments
  • 10/2013-Present SOCRA, CCRP.
  • 2/2011-Present BLS for Healthcare Providers (CPR & AED) Program.
  • 2/2008-Present Phlebotomy (Henry Ford and University of Michigan Experience).
Education
Ph. D:Health Care AdministrationPresentCentral Michigan University, StateHealth Care Administration
Masters of Science:Health Care Administration2012Central Michigan University, StateHealth Care Administration
Bachelors of Science:Biology Psychology2005Central Michigan University, City, StateBiology Psychology
Thesis/Dissertation

PhD dissertation - To be determined.

Experience
Company NameCity, StateClinical Research Associate11/2014 to Current
  • Aortic Aneurysms-Full-time, Paid Design, plan, implement and conduct clinical research Monitor and ensure compliance to study protocols Oversee patient screening and enrollment at study sites Review source documentation, case report forms, and data reports Provide protocol specific training Coordinate meetings Prepare written reports Oversee device accountability Risk management Identify and reconcile corrective and preventive action Attend scientific and medical meetings.
Company NameCity, StateResearch Assistant05/2013 to Current
  • Neurosurgery-Full-time, Paid Community outreach and education Clinical trial management Regulatory duties Institutional Review Board duties Contract/Budget negotiations Study initiation, maintenance and termination Supervisory duties Adverse event reporting Clinical conferences.
Company NameCity, StateClinical Study Coordinator12/2012 to 03/2013
  • Cardiac Surgery-Full-time, Paid Performed study related regulatory duties Institutional review board duties Staff credentialing Adverse event reporting Study initiation and maintenance.
Company NameCity, StateClinical Study Coordinator07/2011 to 09/2012
  • Clinical Trials (Oncology)-Full-time, Paid SWOG, NCI-CCTG, NRG Oncology Group Performed study related regulatory duties Institutional review board duties Credentials Adverse event reporting Study initiation and maintenance.
Company NameCity, StateResearch Assistant05/2011 to 07/2011
  • Public Health Sciences-Full-time, Paid Study of Lifestyle Environment and Fibroids (SELF) Conducted assigned research studies Maintained participant contact Database entries Clerical duties.
Company NameCity, StateResearch Assistant12/2006 to 05/2011
  • Sleep Research Center-Full-time, Paid Institutional Review Board (IRB) duties Data collection, entry, analysis Patient recruitment Conducted assigned research studies Performed testing associated with research studies Reported research to colleagues/Journal Articles Assisted Primary Investigator/IRB and Grant Work.
Company NameCity, StateCaregiver/Administrative Assistant09/2006 to 12/2006
  • Assisted Living-Full-time, Paid Administered medications to residents Performed diabetes testing Assisted in daily activities Clerical duties.
Company NameCity, StateMedical Technician/Resident Assistant05/2004 to 10/2006
  • Assisted Living-Full-time, Paid Administered medications to residents Performed diabetes testing Assisted in daily activities Clerical duties.
Company NameCity, StateVolunteer12/2003 to 01/2004
  • Prepared tools for test samples.
  • Transferred test samples to lab area.
  • Assisted with assigned test.
  • Evaluated test results with lab technician.
Company NameCity, StateOffice Assistant05/2003 to 08/2003
  • Provide clerical assistance.
  • Enter computer data.
  • Prepared documents for legal assistants.
  • Reception duties.
Publications
Steinmiller, C. L., T. A. Roehrs, E. Harris, M. Hyde, M. K. Greenwald and T. Roth (2010). "Differential Effect of Codeine on Thermal Nociceptive Sensitivity in Sleepy Versus Nonsleepy Healthy Subjects." Experimental and Clinical Psychopharmacology 18(3): 277-283. Chhangani, B. S., T. A. Roehrs, E. J. Harris, M. Hyde, C. Drake, D. W. Hudgel and T. Roth (2009). "Pain sensitivity in sleepy pain-free normals." Sleep 32(8): 1011-7. PMC2717191. Harris, E., T. Roehrs, M. Hyde and T. Roth (2009). "Extended Sleep in Sleepy Normals Is Analgesic." Sleep 32: 1255. Harris, E., T. Roehrs, M. Hyde and T. Roth (2009). "A Four-Night Sleep Extension Normalizes Mslt in Sleepy Normals." Sleep 32: 1256. Roehrs, T. A., S. Randall, E. Harris, R. Maan and T. Roth (2011). "Twelve Months of Nightly Zolpidem Does Not Lead to Dose Escalation: A Prospective Placebo-Controlled Study." Sleep 34(2): 207-212. Roehrs, T. A., S. Randall, E. Harris, R. Maan and T. Roth (2011). "Twelve months of nightly zolpidem does not lead to rebound insomnia or withdrawal symptoms: a prospective placebo-controlled study." J Psychopharmacol Epub Ahead of Print. Roehrs, T. A., S. Randall, E. Harris, R. Maan and T. Roth (2011). "MSLT in Primary Insomnia: Stability and Relation to Nocturnal Sleep." Sleep 34(12): 1647-1652. Dasgupta, R., S. Randall, T. Roehrs, E. Harris, R. Maan and T. Roth (2011). "Greater total sleep time is associated with lower pre-sleep salivary cortisol during chronic zolpidem use." Sleep 34(Abstract Suppl): A174. Randall, S., T. Roehrs, E. Harris, R. Maan and T. Roth (2011). "Individual differences in the likelihood of rebound insomnia." Sleep 34(Abstract Suppl): A182. Roehrs, T., S. Randall, E. Harris, R. Maan and T. Roth (2011). "MSLT and total sleep time in primary insomniacs." Sleep 34(Abstract Suppl): A170. Roehrs, T., S. Randall, E. Harris, R. Maan and T. Roth (2011). "Twelve months of nightly zolpidem does not produce withdrawal symptoms on drug discontinuation: A prospective placebo controlled study." Sleep 34(Abstract Suppl): A178.
Memberships/Scholarly Societies

Society of Clinical Research Associates (SOCRA)

Skills

Budget, Contracts, Informed Consent, Good Clinical Practice, Institutional Review Board, FDA, NIH, Community outreach, Clerical/Adminstrative, scientific conferences, Data collection and analysis, Protocol implementation, Patient recruitment, reporting, Risk management, specimen collection, analysis and shipment, AE/SAE reporting, vitals,

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Resume Overview

School Attended

  • Central Michigan University

Job Titles Held:

  • Clinical Research Associate
  • Research Assistant
  • Clinical Study Coordinator
  • Caregiver/Administrative Assistant
  • Medical Technician/Resident Assistant
  • Volunteer
  • Office Assistant

Degrees

  • Ph. D : Health Care Administration Present
    Masters of Science : Health Care Administration 2012
    Bachelors of Science : Biology Psychology 2005

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