Great Sample Resume

Clinical Research Manager Resume

When writing a Clinical Research 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.

This resume example is a great representation of what a hiring manager is looking for in a Clinical Research Manager Resume. Feel free to use this example for reference as you create your own resume or use this easy resume builder that will guide you through every step of your building your resume in just a few minutes.

Here is the Clinical Research Manager Resume example:

Melvin Hays

3850 Red Hawk Road

Holmes City, MN 56341



Job Objective To secure a position with an expanding company as Clinical Research Manager where my education and experience can be utilized to the fullest.

Highlights of Qualifications:

  • Experience in performing clinical research for oncology department
  • Sound knowledge of Federal regulations and clinical trial
  • Profound knowledge of medical terminology
  • Ability to collect and analyze all information
  • Ability to manage multiple projects and prioritize work
  • Ability to prepare research designs
  • Immense Microsoft Application skills
  • Proficient in psychiatric therapies
  • Familiarity to resolve all issues for research
  • Solid understanding of research protocols

Professional Experience:

Clinical Research Manager

Asuragen, Inc., Holmes City, MN

October 2008 – Present

  • Participated in team meetings and provided update on various research strategies.
  • Supervised working of clinical study personnel for all clinical programs.
  • Coordinated with internal and external team to provide research briefings.
  • Assisted supervisors to prepare project schedule and resolve all issues.
  • Determined various activities for functional projects.
  • Designed all long term and short term objectives and established various study objectives.
  • Ensure compliance to all departmental resources requirement.
  • Prepared all medical literature and present it meetings.

Clinical Research Specialist

Sunrise Systems Inc, Holmes City, MN

August 2003 – September 2008

  • Prepared and submitted to all documents to regulatory committees.
  • Monitored clinical research studies and prepared case report forms.
  • Maintained knowledge of protocol requirements according to GCP guidelines.
  • Prepared records of all participants according to standard operating procedures.
  • Managed communication with all sponsors and investigators.
  • Assisted junior clinical research staff to perform research.

Clinical Research Associate

TKL Research, Inc., Holmes City, MN

May 1998 – July 2003

  • Organized and conducted various investigator meetings for clinical research.
  • Prepared all study documents’ according to research protocols.
  • Maintained Trial Master File and provide required update.
  • Performed Trial Master File audit on all internal and external resources.
  • Supervised efficient working contractors and vendors.
  • Evaluated all clinical trial site data according to protocol guidelines.


Bachelor’s Degree in Biological Sciences

Maryville College, Maryville, TN

Master’s Degree in Biological Sciences

William Carey University, Hattiesburg, MS

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  • March 1, 2023Create Date
  • March 1, 2023Last Updated