Data Entry Specialist
QPS, LLC
Summary
The Data Entry Specialist performs duties within the functions of the Data Entry Department, including the maintenance of study related documents, the timely reporting of clinical data to clients and/or regulatory authorities. The Data Entry Specialist must possess strong time management skills in order to effectively compile and manage documents, perform data entry, QC documents, participate in client interaction and requests, and perform short term or long-term projects as required by the department manager and/or department supervisor within contractual timelines.
Job description
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.
Qualifications
- Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as:
- 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
Duties may include more than what is listed and are subject to change without prior notice. Physical requirements for all responsibilities may/do include bending, lifting of papers and files, prolonged sitting and use of stairs
Requirements
- 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
Benefits
- Medical, Dental & Vision
- LTD & Life Insurance
- Paid Holidays
- PTO & Sick Time
- Bonuses
- Work/Life Balance
Company overview
QPS, LLC (also known as QPS Holdings, LLC) is a leading global contract research organization (CRO) founded in 1995 by Dr. Benjamin M. Chien. Originally established as Quest Pharmaceutical Services to provide high-quality bioanalytical LC-MS/MS contract services, the company has grown from a small bioanalysis shop with three employees to a full-service CRO with over 1,200 employees across the United States, Europe, India, and Asia. QPS specializes in providing GLP/GCP-compliant drug development services spanning discovery, preclinical, and clinical phases. The company offers comprehensive expertise in neuropharmacology, drug metabolism and pharmacokinetics (DMPK), toxicology, bioanalysis, translational medicine, and clinical development. With state-of-the-art facilities worldwide, QPS serves pharmaceutical and biotechnology clients by delivering custom-built research solutions, including specialized services for gene therapy, cell therapy, and biomarker development. The company is recognized for its proven quality standards, technical expertise, flexible approach to research, and commitment to client satisfaction.