Data Entry Coordinator at Evolution Research Group

Doral, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Sep, 26

Salary

22.0

Posted On

07 Jun, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Entry, Clinical Data Processing, Quality Control, Case Report Forms, Time Management, Organization, Word Processing, Database Applications, Attention To Detail, Collaborative Communication

Industry

Research Services

Description

About Company: Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally. Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge. Job Description: We are seeking a highly organized and detail-oriented Data Entry Coordinator to join our team. As a Data Entry Coordinator, you will be responsible for the overall coordination, organization, and efficient implementation of clinical data. Complete all study related data entry procedures under the direction of the Site Director. Maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Data Entry Coordinator is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, and company standard operating procedures and policies. Responsibilities: * Performing data entry tasks with a high degree of accuracy and efficiency * Responsible for clinical data processing as directed by Site Director or another assigned manager. Quality control the clinical data to ensure the data quality and report discrepancies to the coordinator. * Complete any training as required by sponsor for access and approval to complete data entry. * Enter data as appropriate for protocol into paper or electronic case report forms. * Track to ensure that data entry is complete for subjects including completed study visits and related forms. * With CRC and/or manager oversight assist Sponsor or CRO data manager with resolution of queries to ensure clinical data quality. * Study, learn, and comply with ERG standard operating procedures and other policies, practices, and regulations where applicable. Minimum Qualifications: * High school diploma or equivalent * Proven experience in data entry or a related field * Proficiency in word processing and database applications * Excellent attention to detail and accuracy * Strong organizational and time management skills Preferred Qualifications: * High School Diploma or equivalent * Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines. * Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner. * Experience working in a clinical or research environment

Responsibilities

The Data Entry Coordinator is responsible for the accurate implementation and processing of clinical trial data under the direction of the Site Director. This includes maintaining confidential participant files and resolving data queries in compliance with GCP and ICH guidelines.