Clinical Data Associate Resume

When writing a Clinical Data Associate 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 Data Associate Resume example:

Edward Hendron

31919 Grand Reserve Pl

Deltona, FL 32738

(555)-555-5555

[email]

Job Objective Seeking a challenging position of Clinical Data Associate position in a reputed organization to utilize my experience and my knowledge to benefit the organization.

Summary Skills

Remarkable experience in clinical data management

Skilled with clinical trial study protocols and web-based data entry systems

In-depth knowledge of data collection, medical terminology, and clinical research principles

Proficient with SAS Base, SAS/AF, SQL, SAS Macro language and SAS/Graph

Good understanding of PPD SOPs, WPDs, ICH/GCP, FDA guidelines

Profound knowledge of regulations related to Data Management and clinical research

Strong organizational skills and excellent attention to detail

Self-motivated, and result-oriented

Excellent interpersonal and conflict resolution skills

Ability to work independently to achieve short- and long-term goals

Work Experience:

Clinical Data Associate, August 2005 to till date

Harris Corporation, Deltona, FL

Designed a database design for new protocols.
Ensured timely and accurate data are delivered to appropriate personnel; and validated database.
Assisted in preparing clinical data budgets and reviewing specified protocols and implemented Clinical Data Management Plans.
Performed data review in conjunction with medical and safety review.
Managed to write queries and updated the database accordingly.
Ensured to code data and that appropriate lock timelines are met.

Clinical Data Associate, May 2000 to July 2005

MediCorp Health System, Deltona, FL

Supervised data management activities and processed to ensure that all goals and objectives are met.
Managed the designing, documentation, testing and implementation of clinical data collection studies.
Developed data systems plans, guidelines, forms, manuals and SOPs.
Contributed to CRF development, database validation, discrepancy management, database lock and generated reports.
Planned, organized, reviewed and evaluated the work of junior data-management professionals and support staff.
Provided appropriate recommendations on hiring, termination, promotion and disciplining.

Education

Bachelor’s Degree in Biological Sciences, Carnegie Mellon University, Pennsylvania, PA