Clinical Research Project Manager Resume

Posted in Resume Samples for Manager

Kelvin Deaton
4865 Oak Way
Fort Calhoun, NE 68023

Job Objective To obtain Clinical Research Project Manager’s position in which I can increase my skills and become a valued member of the team.

Highlights of Qualifications:

  • Outstanding experience to perform clinical research and manage all electronic data collection process
  • Immense knowledge of study monitoring processes
  • Operational knowledge of bio statistics concepts
  • Ability to manage multiple projects efficiently
  • Ability to provide psychiatric treatment
  • Good communication skills
  • Ability to identify and resolve all issues
  • Proficient in understanding good clinical practice
  • Solid understanding of Microsoft Office Applications

Professional Experience:

Clinical Research Project Manager
Bartech Group, Fort Calhoun, NE
October 2008 – Present

  • Prepared study design and implemented all protocols.
  • Coordinated with various teams and designed clinical research projects.
  • Provided technical support to all sales personnel and employees.
  • Ensued compliance to Quality system and international standards.
  • Assisted clinical investigators to perform clinical research on orthopedics.
  • Analyzed study objectives and prepared appropriate strategies.
  • Maintained all statistical data and prepared reports for clinical data.
  • Prepared orthopedic medical literature and evaluated it regularly.

Clinical Research Project Assosciate
LDR Spine USA, Inc., Fort Calhoun, NE
August 2003 – September 2008

  • Performed regular review for all projects and achieved objectives.
  • Coordinated with work groups and ensure compliance to timeframe.
  • Prepared efficient schedule for training plans for internal and external teams.
  • Participated in various project team meetings and maintained files.
  • Performed research on all investigation sites.
  • Maintained trial management tools and provided update.

Jr. Clinical Research Associate
Kensey Nash Corporation, Fort Calhoun, NE
May 1998 – July 2003

  • Monitored clinical visits and assisted in follow up.
  • Participated in all project management teleconferences on weekly basis.
  • Developed study associated monitoring tools for research project.
  • Performed regular agency audit on all clinical sites.
  • Evaluated study tools and prepared source documents worksheets.
  • Maintained confidentiality of information and ensure compliance to strict code.


Bachelor’s Degree in Life Science
Xavier University, Cincinnati, OH

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