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Researcher Data Entry Jobs in New Port Richey, FL

Socket.dev

Clinical Research Coordinator

Largo, FL · On-site

$60 - $80/hr

Description GENERAL SUMMARY Clinical Research Coordinator works under Clinical Research Managers ... Case Report Form (CRF) Entries and Management - includes data entry, query resolution in paper and ...

Holland & Knight

Payroll Specialist

Tampa, FL

$22.25 - $30.25/hr

Address inquiries and research issues in an accurate and timely manner. * Assist with regular audit of data entry records. * Maintain accurate firmwide records. * Specialprojectsanddutiesassigned.

Briggs Equipment

Parts Research Analyst

Tampa, FL · On-site

The Parts Research Analyst provides customer service for the Parts Operation Center or assigned ... High attention to detail, to include precise data entry * Excellent verbal and written ...

Imagenet

Mailroom Scanning Clerk - Tampa, FL

Tampa, FL · On-site

$15/hr

Research mail and document details as needed to ensure proper handling Operational Support * Perform data entry and maintain accurate records * Coordinate with internal teams to support timely and ...

Imagenet

Mailroom Scanning Clerk - Tampa, FL

Tampa, FL · On-site

$15/hr

Research mail and document details as needed to ensure proper handling Operational Support * Perform data entry and maintain accurate records * Coordinate with internal teams to support timely and ...

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All JobsResearcher Data Entry JobsResearcher Data Entry Jobs in New Port Richey, FL

Researcher Data Entry information

See New Port Richey, FL salary details

$26.7K

$100.7K

$146.5K

How much do researcher data entry jobs pay per year?

As of Sep 12, 2026, the average yearly pay for researcher data entry in New Port Richey, FL is $100,739.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,700.00 and $137,200.00 per year, depending on experience, location, and employer.

What is a researcher data entry?

Researcher Data Entry jobs involve collecting, organizing, and inputting data for research projects or studies. Individuals in this role are responsible for ensuring that data is accurately recorded and maintained in databases or spreadsheets. They often work with large volumes of information, verify the integrity of data, and may assist with basic data analysis. Researcher Data Entry professionals support research teams by making sure that the information is accessible and reliable for further analysis or reporting.

What are the key skills and qualifications needed to thrive as a researcher data entry?

To thrive as a Researcher Data Entry professional, you need strong attention to detail, accuracy, and proficiency in data management, typically supported by a high school diploma or relevant coursework. Familiarity with spreadsheet software such as Microsoft Excel, database management systems, and data entry tools is essential. Outstanding organizational skills, time management, and the ability to work independently make someone stand out in this position. These skills are crucial for ensuring the integrity and reliability of research data, which forms the foundation for sound analysis and decision-making.

How does a researcher data entry professional typically collaborate with other members of a research team?

A Researcher Data Entry professional often works closely with researchers, analysts, and project managers to ensure accurate and timely data collection and entry. They may attend regular team meetings to discuss project progress, clarify data requirements, and address any discrepancies found during data input. Effective communication and attention to detail are essential, as their work directly supports the validity and reliability of research outcomes. Collaboration tools and shared databases are commonly used to streamline workflow and maintain data integrity across the team.

What is the difference between Researcher Data Entry vs Data Analyst?

AspectResearcher Data EntryData Analyst
Required SkillsData entry, basic research, attention to detailData analysis, statistical skills, data visualization
Work EnvironmentResearch labs, academic institutions, data collection settingsBusiness offices, analytics firms, corporate environments
Common TasksInputting research data, organizing datasets, verifying accuracyInterpreting data, creating reports, identifying trends

Researcher Data Entry primarily focuses on inputting and managing research data with an emphasis on accuracy and organization. Data Analysts, however, analyze datasets to extract insights and support decision-making. While both roles require attention to detail, Data Analysts typically need stronger analytical and statistical skills. The roles often overlap in data handling but differ significantly in scope and complexity.

What cities near New Port Richey, FL are hiring for Researcher Data Entry jobs?

Cities near New Port Richey, FL with the most Researcher Data Entry job openings:

Researcher Data Entry jobs near you
Infographic showing various Researcher Data Entry job openings in New Port Richey, FL as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 9% Part Time, and 3% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $100,739 per year, or $48.4 per hour.

Clinical Research Coordinator

Largo, FL • On-site

Solaris Health Holdings LLC
See more jobs at Solaris Health Holdings LLCexternal

$21 - $27.75/hr

Full-time

Posted 16 days ago

Job description

Description

GENERAL SUMMARY 


Clinical Research Coordinator works under Clinical Research Managers and are tasked with administering clinical trials. Responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.   






Requirements

ESSENTIAL JOB FUNCTION/COMPETENCIES 

The responsibilities and duties described in this job description are intended to provide a general overview of the position. Duties may vary depending on the specific needs of the affiliate or location you are working at and/or state requirements. Responsibilities include but are not limited to:


  • Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals.
  • Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol.
  • Coordination and management of the clinical trial, communication with sponsor and authorities, visit coordination, sampling, time management and product accountability.
  • Data collection and management, collection and development of source documents, use of CRFs, managing patient registration, AEs, filing and archiving, managing monitoring visits, dealing with queries.
  • Maintain accurate records of the receipt, inventory, and dispensation of study drug and obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol.
  • Patient visits, data collection and transcription/EDC, prepare for monitor visits, protocol adherence to include height, weight, blood pressure, respirations, pulse temperature, O2 saturation.
  • Schedule appointments and organize materials to be used during study visits and ensure that all required tests are completed for each study visit per protocol.
  • Includes initial study start-up information/ requirements, dissemination of updated Investigator's Brochures, protocols and informed consent information, online training initiated by sponsor, review of correspondence throughout study.
  • Completes Source Documentation-which includes completing and uploading all necessary documents to CRIO and maintaining all charts properly.
  • Medical Assessment-includes obtaining information from patient or chart regarding name of medication, start and stop dates, dose, and indication.
  • Biological Sampling Collection/Packaging/Shipping - includes serum and/or tissue collection, processing, packaging and shipping per study specific requirements.
  • Case Report Form (CRF) Entries and Management - includes data entry, query resolution in paper and/or electronic CRFs.
  • Investigational Product (IP) Management - includes receiving IP supplies, IP accountability, monitoring of temperature controls, destructions or return of IP.
  • Develop and/or Maintain Essential Documents - includes study specific training documents, study specific logs, patient questionnaires, patient pill diaries, lab requisition forms, other study specific forms.
  • Supply Chain Maintenance-Supplies Inventoried, stocking, organizing, and resupply order placed as required. Completed in Envi system.
  • Study Coordination- rooming, administer questionnaires, scheduling scans, set up room for procedures and wipe and clean equipment after procedures and visits.
  • Obtain/Maintain all required training- GCP, IATA,CPR Occasionally help the study coordinators at other offices such as the surgery center.
  • Performs other position related duties as assigned.
  • Employees shall adhere to high standards of ethical conduct and will comply with and assist in complying with all applicable laws and regulations. This will include and not be limited to following the Solaris Health Code of Conduct and all Solaris Health and Affiliated Practice policies and procedures; maintaining the confidentiality of patients' protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA); immediately reporting any suspected concerns and/or violations to a supervisor and/or the Compliance Department; and the timely completion the Annual Compliance Training.


CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS


  • BLS certification required, ACLS preferred.
  • License and certification as required by state.
  • Medical Assistant required
  • LPN a plus
  • Urology experience preferred


KNOWLEDGE | SKILLS | ABILITIES


  • Knowledge of medical terminology, healthcare coding systems, and clinics functions.
  • Must be able to function in a team-oriented environment, display strong analytical, investigative, interpersonal and organizational skills, pay high attention to detail with consistent follow-through and be able to productively manage high volumes of work.
  • Knowledge of database management.
  • Maintain a working knowledge of all assigned study protocols and amendments.
  • Excellent verbal and written communication skills.
  • Skill in using computer programs and applications including Microsoft Office.
  • Delivers exceptional patient service throughout all interactions.
  • Excellent organizational skills and attention to detail.
  • Strong analytical and problem-solving skills.
  • Complies with all health and safety policies of the organization.
  • Complies with HIPAA regulations for patient confidentiality.
  • Ability to work independently and manage deadlines.
  • Ability to establish and maintain effective working relationships with patients, colleagues, physicians and the public; successfully manages interactions with challenging or difficult people.
  • Ability to deal compassionately, professionally, and courteously with patients, their families, physicians, and staff.
  • Ability to build relationships with patients and display empathy and compassion to patients.


EDUCATION REQUIREMENTS

  • High School Diploma or equivalent required.


EXPERIENCE REQUIREMENTS


  • 1-3 years of related experience preferred.


REQUIRED TRAVEL


  • Minimal travel required.


PHYSICAL DEMANDS


Carrying Weight Frequency

1-25 lbs. Frequent from 34% to 66%

26-50 lbs. Occasionally from 2% to 33%

Pushing/Pulling Frequency

1-25 lbs. Seldom, up to 2%

100 + lbs. Seldom, up to 2%

Lifting - Height, Weight Frequency

Floor to Chest, 1 -25 lbs. Occasional: from 2% to 33%

Floor to Chest, 26-50 lbs. Seldom: up to 2%

Floor to Waist, 1-25 lbs. Occasional: from 2% to 33%

Floor to Waist, 26-50 lbs. Seldom: up to 2%



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