Remote Data Entry Specialist / Part-time

Recruit Monitor; San Antonio (TX); Remote; USD 20,664 - 27,552; Part time

Job summary

A data management firm is looking for a motivated Remote Data Entry Specialist for part-time work focused on clinical trials. The ideal candidate will have a High School Diploma and at least 1-2 years of experience in data entry. Responsibilities include transcribing data, verifying integrity, and assisting with quality control in electronic data capture systems. Strong organizational skills, attention to detail, and the ability to work independently are essential. This role offers a chance to adapt during the company’s growth phase.

Qualifications

• Ability to work independently with minimal supervision.
• Ability to effectively collaborate with other team members.
• Flexible during the company's growth stage.

Responsibilities

• Transcribe source data into various electronic data capture (EDC) systems.
• Verify integrity of data by comparing it to source documents.
• Assist clinical team with quality controls (QC) of patient files.

Skills

High attention to detail

Strong organizational skills

Time management skills

Ability to perform repetitive tasks

Education

High School Diploma

Tools

Microsoft Office

EDC systems knowledge

Job description

Remote Data Entry Specialist / Part-time

About the job Remote Data Entry Specialist / Part-time

We areseeking a highly motivated Data Entry Specialist to assist with a variety of ongoing clinical trials. We are looking for someone who can take initiative and provide real time data entry for our clinical trials.

Someone who has worked in a high paced, fast-moving environment will work well at Paychex. Previous research experience is strongly preferred.

• Transcribes source data into various electronic data capture (EDC) systems per protocol requirements and following established standards
• Verifies integrity of data by comparing it to source documents
• Follow established standard operating procedures (SOPs), good clinical practice (GCP) and other applicable regulatory requirements in the execution of all EDC activities
• Answer queries within EDC system in a timely manner
• Assist the clinical research team with quality controls (QC) of patient files per ERAs established standards
• Prepare and scan documents into EDC systems and ERAs database
• Assist the clinical team with preparing for onsite monitoring visits for each study protocol

Requirements

• High School Diploma
• High attention to detail
• Ability to perform repetitive tasks with a high degree of accuracy
• Strong organizational and time management skills
• Flexible during the companys growth stage
• Ability to work independently with minimal supervision
• Ability to effectively collaborate with other team members

Desired Skills & Qualifications

• 1-2 years of experience in data entry
• Experience with Microsoft Office
• Knowledge of research EDC systems preferred (Veeva Vault, Medrio, IBM, OpenClinica, MedidataRAVE, etc..)