Clinical Data Entry Jobs in Arkansas

Minimum 3-5 years of experience in a pharmaceutical/CRO setting with at least 3-4 years of experience in Data Management.

Liaise closely with the Lead Data Manager to report study progress and any issues outstanding.

Assist the Lead Data Manager with the preparation of study documentation.

Assist the Lead Data Manager with the creation and validation of Manual and SAS checks.

Proficient knowledge of CDISC CDASH and SDTM terminology

Attend study update meetings or calls with the study sponsor as needed.

Accurately enter patient data into the Laboratory Inventory Management System (LIMS).

Good oral and written communication skills including excellent knowledge of correct spelling, grammar, and punctuation

Perform data entry for a specific product and case type with high accuracy and efficiency.

Must maintain current status on Natera training requirements.

Previous computer experience is required.

Flexible in work time and shift as work schedule may be modified to meet operational requirements

Provides data entry and management support to an assigned caseload of research protocols

To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:

Reviews study protocols and assists in the planning and implementation of the data management aspects of clinical research projects

Possession of a Bachelor's degree from an accredited college/university, or qualifying experience in lieu of required education

Cloud–based clinical data management systems (e.g., Medidata Rave) and enrollment tracking systems (e.g., OPEN)

Works collaboratively with VRS team members, site staff, and data monitors to meet program and protocol requirements, deadlines, and deliverables

Pharmacy technician certification plus 2 years related work experience, or 4 years related work experience.

Demonstrated ability to effectively communicate with management and other team members

Demonstrated ability to apply pharmacy knowledge and experience in critical thinking and problem solving; ability to recognize discrepancies in data

Perform data normalization prior to data entry, using controlled terminology and following strict editorial guidelines

Strong computer skills; familiarity with Microsoft Office products (e.g., Word, Excel, Access) and Adobe Professional

Solid knowledge of internet searching and pharmaceutical terminology

· Gathering & documenting and confirming requirements, designing solutions, obtaining SME

· Certifications Required: Epic Clarity, Caboodle and Clinical Data Model (or legacy equivalents)

·Strong listening and communications skills to understand purpose of requests, as well as

·collaboratively ironing out requirements interpretation for mandatory submissions to

·Experience working with end user analyst level as well as subject matter expert, director-level leadership.

· IP nursing monitoring compliance

Strong organizational skills with experience balancing priorities and resources

Working closely with Clinical Leads and Project Managers to ensure all data is uploaded and entered in a timely manner

Strong skills in the use of technology, tools, operating systems, and software and is comfortable using these daily

Experience with electronic data capture (EDC) systems, including Oracle Clinical and/or Medidata Rave

2.Data Entry: You will be responsible for all data entry

6.Misc. Responsibilities as needed or required by projects.

Bachelors + 4 Years Data Management Experience OR Masters and 2 Years of Data Management

Develop and review data management procedures for clinical trials with sponsor companies and other departments;

Design reports and metrics that are useful management tools for your projects;

Attend and participate in teleconferences and face-to-face meetings with sponsor companies as the lead representative from data management;

May provide project data management training as needed regarding CRF Completion or EDC system usage;

Coordinate overall data management by serving as primary contact for the sponsor, external data providers, and all project team members

Support data management activities for multiple study protocols

Provide input on study-related documents, such as case report forms and data management plan

Review study-specific documentation to obtain understanding of study-specific data processing requirements

Collaborate with the Clinical Data Manager to develop manual review listing(s) and conduct manual review

Keep Clinical Data Manager informed of data status and issues

Minimum 1 year work experience, healthcare or clinical research setting preferred

Maintain compliance with job specific proficiency requirements, including CCT certification (RN or Paramedic may qualify)

This is a remote/work from home position, a strong internet connection will be necessary.

Support AT Clinical Operations by performing daily administrative responsibilities.

Provide feedback regarding any systems or concerns to the AT Clinical Operations Manager

Knowledge of medical terminology preferred.

Strong PC proficiency including working knowledge of Microsoft Outlook, Excel, Adobe, and PowerPoint

Strong administrative skills and prior experience with data entry

Assist with large scale data entry, inputting relevant data into the database.

At least 2 years previous work experience in a clinical manufacturing environment

Sound knowledge of MS Office and computer literate

Fully remote anywhere in US

Please click ‘apply’ or contact Sam Chapple (Recruitment Manager, APAC) at Planet Pharma for more information:

Strong administrative skills and prior experience with data entry

Assist with large scale data entry, inputting relevant data into the database.

At least 2 years previous work experience in a clinical manufacturing environment

Sound knowledge of MS Office and computer literate

Fully remote anywhere in US

Please click ‘apply’ or contact Sam Chapple (Recruitment Manager, APAC) at Planet Pharma for more information: