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.

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Here is the Clinical Research Manager Resume example:

Melvin Hays

3850 Red Hawk Road

Holmes City, MN 56341

(555)-555-5555

[email]

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.

Education

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, 2020Create Date
  • March 1, 2020Last Updated