Data Entry Specialist

QPS, LLC•Springfield, MO

29d•Onsite

About The Position

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Stage Clinical and Phase I IV Clinical Research services. We welcome individuals who want to be part of our growing organization. QPS is an innovative, dynamic organization that strives to employ talented, caring and committed employees who will work collaboratively towards achieving our mission of improving human health and the quality of life. QPS offers challenging and rewarding work in its four core business areas and support functions. Underpinning the operation is a culture that values diversity, innovation and accountability. Employees are encouraged to take responsibility and achieve their best, both as individuals and as team members.

Requirements

Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role
High School diploma or equivalent
Previous data management and Microsoft Office experience desired (at least 6 months)
Good time management, organizational and interpersonal skills
Good written and oral communication
Ability to work independently and as a team
Consistency in delivering positive results, following through with tasks from start to finish

Responsibilities

Develop a full understanding of Standard Operating Procedures, study protocols and data entry guidelines for multiple clinical trials and effectively organize study specific information for efficient recall.
Perform all department tasks within pre-defined contractual timelines and according to Standard Operating Procedures, study protocols, and data entry guidelines.
Compile and interpret data gathered from clinical trials in order to accurately transcribe the data into paper or electronic case report forms.
100 % review of all source documents and case report forms in order to analyze, identify, query and resolve data issues and inconsistencies, ensuring quality reporting standards are met through an established Quality Control process.
Customer service, including effective communication with other staff and/or clients regarding client visit preparation, client requests and assisting with the completion of both internal and external queries in a timely manner.
Audit the contents of all source document folders after trial completion to ensure completeness and accuracy, assisting with resolution of any issues prior to archiving the study files.
Source document organization, management and filing.