Recruit Monitor
Remote Data Entry Specialist / Part-time
Recruit Monitor, San Antonio, Texas, United States, 78208
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..)
#J-18808-Ljbffr
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..)
#J-18808-Ljbffr