Clinical Research Project Manager Resume

When writing a Clinical Research Project Manager Resume remember to include your relevant work history and skills according to the job you are applying for. Whether you're seeking an entry-level position or have been in your career for a few years, exposing your relevant achievements in your resume can allow you to stand out and get that job interview.

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Here is the Clinical Research Project Manager Resume example:

Kelvin Deaton

4865 Oak Way

Fort Calhoun, NE 68023

(555)-555-5555

[email]

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.

Education

Bachelor’s Degree in Life Science

Xavier University, Cincinnati, OH

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  • March 1, 2020Create Date
  • March 1, 2020Last Updated