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.

CREATE YOUR RESUME

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