Clinical Research Medical
Resume:
Lindsey Brewer
Wichita KS, ***** PH 316-***-****
***********@*******.***
Objective
To obtain a position in your healthcare organization that utilizes my experience in program management,
process improvements and implementation, and client relations.
Professional Summary
Certified Clinical Research Coordinator who throughout the past 6 years with Heartland Research has gained
quality experiences which has enabled me to become a goal-oriented professional with a track record of
consistently meeting and exceeding established goals and objectives related to management, training, and
education. My skills include building long-term relationships with multiple levels of professional individuals
as clients and future customers. I am passionate about achieving significant results related to promoting
organizational growth, securing necessary industry-related designations, and increasing overall client volume.
I am highly motivated and ambitious with excellent interpersonal communication, relationship management,
and presentation skills.
Professional Experience and Achievements
May 2013 – Current Business Development Associate / Clinical Research Coordinator
Level II
Heartland Research Associates
Wichita, Kansas
Continue to hold duties of Clinical Research Coordinator advising and assisting other CRCs
on study related issues while managing new responsibilities as a Business Development
Associate
Effectively create marketing strategies for all clinical trials at the same time
Create recruitment campaigns and following campaign from start to finish
Enhance and grow working relationships with existing clients
Communicate with appropriate staff to obtain information so decisions can be made which
advertising and marketing efforts to pursue
Maintain familiarity with medical community as a whole
Assist in enhancing company’s name and image recognition
Assist in the review and implementation of new business ideas
Monitor advertising and marketing trends relating to business development and patient
recruitment
Create advertisements for each means of advertising to submit and gain sponsor and IRB
approval
Coordinate production and placement of advertisements appropriately, maintain budgets
June 2010 – May 2013 Clinical Research Coordinator
Effectively devote keen and acute attention to detail while coordinating and initiating
anywhere from 6-15 clinical research studies on a weekly basis
Met and exceeded sponsor specified patient enrollment goals on a monthly basis
Possess the ability to be a self-starter, along with developing the ability to work as a team
player while managing a variety of clinical related projects.
Function independently without close supervision, and consistently exercise discretion and
the highest level of good clinical judgment
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Ability to quickly adapt to working in a wide variety of dynamic areas within the field of
clinical research
Ability to multi-task and perform multiple critical tasks simultaneously
Effectively communicate with company sponsors concerning all aspects of business
activities
Adhering to ICH-GCP guidelines
March 2009 – June 2010 Patient Referral Specialist
Recruited and screen potential study participants in accordance with each sponsor’s protocol
inclusion/exclusion criteria.
Maintained familiarity with investigational as well as FDA approved pharmaceutical agents
Developed and maintained a keen awareness of each potential company sponsor’s specific
goals, requirements, protocols and procedures to ensure that study activities are correctly
completed.
Educated and train physicians and study investigators in study protocols.
Created and implement recruitment plans for various medical studies.
Reviewed regularly and on an “as needed” basis, all potential patient medical charts. Utilize the
appropriate database for completion of this task.
December 2007 – March 2009 Sponsor Liaison
Served as liaison between company and peer organizations, communicating various issues and
troubleshooting and resolving problems.
Organized/reviewed/maintained/updated files of current studies as well as education logs for all
employees and private investigators
Processed emails and phone messages from clinical research associates with outstanding items
Reviewed reports concerning on-going business transactions, as well as those which were
closing/closed, for outstanding issues prior to the next review; discussed strategies with team
members both before and after reviews
Entered, updated and maintained associates contact information
Built and maintained good rapport with outside pharmaceutical associates
SKILLS/Certifications
Understanding and reviewing Search Engine Marketing and Retargeting
Interpreting Google Analytics
Ability to manipulate company website to ensure current and accurate information
Certified Clinical Research Coordinator – Received certification March of 2014 through
Association of Clinical Research Professionals
EDUCATION
University of Kansas
Lawrence, Kansas
August 2003 – December 2007
Bachelor of Science/Arts in Health and Exercise Sciences
LEADERSHIP/ACTIVITIES
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Young Professionals of Wichita
– Active Pulse Action Team member. Pulse team members coordinate events which facilitate
new young professional peer connections while helping members expand their awareness of
different social/entertainment options available in Wichita
Kickin’ it for the Kids –
Participant in a fundraiser event hosted by Red Shoe Society of Wichita which raises awareness
for Ronald McDonald House Charities
Enhance Wichita – Community
enhancement volunteer project. Active volunteer to enhance and beautify neighborhoods in the
Wichita community. Since 2009, this team has led the revitalization of 50 homes with over
$200,000 worth of work.
Member of ACRP –Association
of Clinical Research
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