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Pra Health Sciences - Sr Clinical Research Associate Resume Example

Aiden Jackson
  • XXXXXX XXXXXXX XXX, Hampshire, IL 60140
Professional Summary
Accomplished and energetic Clinical Research Associate eager to utilize my education and skills to facilitate a career change.  
  • Strong communication skills
  • People oriented
  • Computer proficient
  • Detail driven
  • Leadership potential
  • Ambitious to be productive
Sr. Clinical Research Associate, 09/2014 to 04/2015
PRA Health Sciences Austin, TX
  • Implemented and monitored clinical trials to ensure sponsor and investigator obligations were met and were compliant with applicable local regulatory requirements and ICH-GCP guidelines
  • Assessed the qualification of potential investigative sites, initiated clinical trials at investigative sites, instructed site personnel on the proper conduct of clinical trials at investigative sites
  • Reviewed and verified accuracy of clinical trial data collected
  • Worked closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
  • Performed essential document site file reconciliation
  • Performed source document verification and query resolution
Clinical Research Associate III, 07/2013 to 09/2014
ICON Austin, TX
  • Monitored sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs/WPDs, applicable regulations and the principles of ICH-GCP
  • Provided a benchmark of monitoring competence to inexperienced/less experienced colleagues
Clinical Research Associate - Contract, 12/2012 to 06/2013
Parexel Austin, TX
  • Assured adherence to GCP, Investigator integrity and compliance with all study procedures
  • Performed site management activities including all in-house and on-site monitoring for all visit types
  • Mentored and trained new Clinical Research Associates
Clinical Research Associate (CRA), 08/2008 to 05/2012
PPD Austin, TX
  • Conducted site visits to determine regulatory compliance and prepared required documentation
  • Developed collaborative relationships with investigative sites and client company personnel
Clinical Regulatory Specialist, 10/2007 to 10/2008
PPD Austin, TX
  • Facilitated effective communication between client company, vendors and project team in order to anticipate, identify and resolve issues for non-clinical/clinical aspects of assigned studies
  • Accountable for the review and transmission of regulatory documents
  • Accountable for generating, resolving and clarifying queries and regulatory documents
Project Assistant, 12/2006 to 10/2007
PPD Austin, TX
  • Provided day-to-day administrative support to study teams
  • Maintained central study files for assigned projects
  • Assisted with the identification of potential investigators
  • Trained and mentored new Project Assistants for the department
Intern, 08/2006 to 12/2006
PPD Austin, TX
  • Obtained experience in numerous departments
  • Corresponded regularly with investigators, team members and sponsors on various project related issues
  • Tracked important study related information in PPD databases and offered organizational and administrative expertise
Bachelor of Science: Health, Dec 2006 Texas A&M University - College Station, TX
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Resume Details

This is a real resume for a Sr Clinical Research Associate in Hampshire, Illinois with experience working for such companies as Pra Health Sciences, Icon, Parexel. This is one of the hundreds of Sr Clinical Research Associate resumes available on our site for free. Use these resumes as templates to get help creating the best Sr Clinical Research Associate resume.

Previous Companies:

  • PRA Health Sciences
  • ICON
  • Parexel

Previous Job Positions:

  • Sr Clinical Research Associate
  • Clinical Research Associate III
  • Clinical Research Associate Contract
  • Clinical Research Associate
  • Clinical Regulatory Specialist


  • Texas A&M University

Level of Education:

  • Bachelor of Science

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