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Senior Data Entry Simple Typing Jobs in Delaware

Bright Brothers

Appointment Scheduler

Ellendale, DE · On-site

$16/hr

Ensures all paperwork, data entry, and correspondence are accurate, timely, and completed according ... Our mission is simple: to be the exterior washing and holiday lighting company of choice, by ...

Relativity

Senior Billing Specialist

Wilmington, DE · On-site

$60K - $90K/yr

The Senior Billing Specialist is a key contributor to the OTC team, responsible for the accurate ... Accounts Receivable (AR), Billing, Communication, Customer Service, Data Entry, Enterprise Resource ...

PRICE AUTOMOTIVE GROUP

RECEPTIONIST

Newark, DE

$15.50 - $20.25/hr

Perform filing, typing and data entry as necessary * Maintain a safe driving record, may be called on to assist in vehicle delivery or pickup * Attend periodic production and safety meetings * Follow ...

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Senior Data Entry Simple Typing information

What are Senior Data Entry Simple Typing jobs?

Senior Data Entry Simple Typing jobs involve accurately entering, updating, and managing data using computer systems, often focusing on basic typing tasks. Senior professionals in this role may handle more complex data sets, ensure data quality, and may oversee or train junior data entry staff. They are expected to have fast typing skills, excellent attention to detail, and experience with various data entry software. These roles are critical for maintaining accurate records in organizations across industries.

What are some common challenges faced by Senior Data Entry professionals, and how can they effectively manage large volumes of data?

Senior Data Entry professionals often encounter challenges such as maintaining accuracy while processing high volumes of information and meeting tight deadlines. To manage these challenges, it's important to develop strong attention to detail, utilize keyboard shortcuts, and become proficient with data management software like Microsoft Excel or Google Sheets. Collaborating closely with team members and supervisors can also help clarify priorities and ensure consistency across projects. Regular breaks and an organized workflow can further reduce errors and improve productivity.

What are the key skills and qualifications needed to thrive as a Senior Data Entry Simple Typing professional, and why are they important?

To thrive as a Senior Data Entry Simple Typing professional, you generally need fast and accurate typing skills, attention to detail, and a high school diploma or equivalent. Familiarity with data entry software, spreadsheets (like Microsoft Excel or Google Sheets), and basic office systems is typically required. Strong organizational skills, time management, and reliability help professionals excel in this role. These competencies ensure data integrity, efficiency, and the smooth handling of large volumes of information.

What is the difference between Senior Data Entry Simple Typing vs Data Entry Clerk?

AspectSenior Data Entry Simple TypingData Entry Clerk
CredentialsBasic computer skills, typing proficiencyBasic computer skills, typing proficiency
Work EnvironmentOffice, remote, data centersOffice, remote, data centers
Industry UsageVarious industries requiring data inputVarious industries requiring data input
Job ResponsibilitiesInputting data, minimal supervisionInputting data, verifying accuracy

Both roles involve data entry tasks with similar credentials and work environments. The main difference is that Senior Data Entry Simple Typing may involve more complex or high-volume tasks, while Data Entry Clerks focus on routine data input and verification. The senior role may also require more experience but generally shares similar skills and industry usage.

Senior Data Entry Simple Typing jobs near you
Senior Clinical Research Associate

Senior Clinical Research Associate

AstraZeneca

Wilmington, DE • On-site

Full-time

Posted 9 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

18th of 74 rated pharmaceutical

Job description

This is what you will do:
The Senior Clinical Research Associate (Sr. CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The Sr. CRA works in close collaboration with (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. The Sr. CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery and compliance of the study.
The Sr. CRA is responsible for the selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
A Sr. CRA with demonstrated skillset and experience may take on additional responsibilities and tasks as needed (eg. Lead CRA, etc).
You will be responsible for:
  • Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP).
  • Driving performance at the sites. Proactively identifying and ensuring timely resolution to study-related issues and escalate them as appropriate.
  • Training, supporting and advising Investigators and site staff in study related matters, including Risk Based Quality Management (RBQM) principles.
  • Development of recruitment plans with each site and managing and supporting enrollment to ensure sites and studies meet enrollment milestones. Document recruitment barriers and mitigation plans.
  • Ensure agreed monitoring KPIs are observed and remain within the agreed quality acceptable ranges (Action Items aging, SDV metrics, Data entry metrics, query aging, MV reports metrics, etc.)
  • Preparing and finalizing monitoring visit reports in CTMS and provide timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with Alexion SOPs.
  • Ensuring timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, Alexion SOPs and local requirements. Supporting/participating in regular QC checks of the eTMF
  • In some countries, as required, CRAs are accountable for study start-up and regulatory maintenance. Tasks may include collection, preparation, review and tracking of documents for the application process; submission of proper application/documents to EC/IRB and to Regulatory Authorities for start-up and for the duration of the study.
  • Contributing to the nomination and selection of potential investigators and assisting with feasibility activities
  • Collaborating with local Medical Affairs, Medical Advisor Pipeline (MAP) and other internal stakeholders, as needed.
  • Following quality issue processes by escalating systematic or serious quality issues, data privacy breaches, or ICH-GCP compliance issues to PMCO, Director COM, HCO and/or Quality Group as required.
  • Preparing for and collaborating with the activities associated with audits and regulatory inspections in liaison with PMCO, Director COM, and Quality Group.

You will need to have:
  • Minimum of 4 years of CRA monitoring experience
  • Bachelors degree in related discipline, preferably in life science, or equivalent qualification
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
  • Excellent knowledge of relevant local regulations.
  • Good medical knowledge and ability to learn relevant Alexion Therapeutic Areas.
  • Good understanding of the drug development process.
  • Excellent understanding of Clinical Study Management including monitoring, study drug handling and data management.
  • Excellent attention to detail.
  • Excellent written and verbal communication skills.
  • Excellent collaboration and interpersonal skills.
  • Good negotiation skills.
  • Demonstrates flexibility in schedule and willingness to travel (required travel may be as high as 70% during busy periods)
  • Valid driving license

We would prefer for you to have:
  • Ability to work in an environment of remote collaborators and in a matrix reporting structure
  • Manages change with a positive approach for self, team and the business. Sees change as an opportunity to improve performance and add value to the business.
  • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
  • Proactivity and assertive when communicating with internal stakeholders and sites
  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment.
  • Team oriented and flexible; ability to respond quickly to shifting demands and opportunities.
  • Experience in all study phases and in rare medical conditions preferred.

Date Posted
16-Jul-2026
Closing Date
22-Jul-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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