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Remote Data Entry Simple Typing Jobs in San Ramon, CA

Twilio

Senior Product Marketing Manager, Data

San Francisco, CA · Remote

$142.40K - $186.50K/yr

Our dedication to remote-first work, and strong culture of connection and global inclusion means ... You have a proven ability to synthesize complex, technical product features into simple, value ...

Gophermods

Sales Support Administrator

San Jose, CA · On-site +1

$24 - $29.50/hr

Strong attention to accuracy in data entry, documentation, and follow-through * Excellent ... Fully remote/virtual position * Hours: Monday - Friday, 8:00 AM - 4:00 PM CST * Must be available ...

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Remote Data Entry Simple Typing information

See San Ramon, CA salary details

$12

$21

$31

How much do remote data entry simple typing jobs pay per hour?

As of May 29, 2026, the average hourly pay for remote data entry simple typing in San Ramon, CA is $21.76, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $24.42 per hour, depending on experience, location, and employer.

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

To thrive in Remote Data Entry Simple Typing, you need fast and accurate typing skills, attention to detail, and basic computer literacy, typically supported by a high school diploma or equivalent. Familiarity with spreadsheet software (like Microsoft Excel or Google Sheets), data management systems, and sometimes CRM platforms is usually required. Strong organizational skills, time management, and the ability to work independently help individuals excel in a remote environment. These capabilities ensure data is entered quickly and correctly, supporting business operations and minimizing costly errors.

What are some common challenges faced when working as a Remote Data Entry Simple Typing professional, and how can they be managed?

One common challenge in remote data entry is maintaining focus and accuracy while working independently, especially in repetitive tasks. Distractions at home and monotony can lead to errors, so it's important to establish a dedicated workspace and take regular breaks to stay refreshed. Using productivity tools and double-checking your work can help ensure data integrity. Additionally, clear communication with supervisors and team members is crucial for resolving any ambiguities in the data or instructions.

What is a Remote Data Entry Simple Typing job?

A Remote Data Entry Simple Typing job involves entering, updating, or managing data in digital formats from a remote location, usually from home. Employees in these roles are responsible for typing information from various sources into databases, spreadsheets, or other computer systems accurately and efficiently. These jobs typically require basic computer skills, attention to detail, and the ability to work independently. Most positions offer flexible hours and may be part-time or full-time, making them popular for those seeking remote work.

What is the difference between Remote Data Entry Simple Typing vs Remote Data Entry with Advanced Software Skills?

AspectRemote Data Entry Simple TypingRemote Data Entry with Advanced Software Skills
Required CredentialsBasic computer literacy, typing skillsBasic computer literacy, familiarity with software tools
Work EnvironmentHome-based, minimal equipmentHome-based, may require specific software installations
Employer & Industry UsageCommon in administrative, healthcare, retail sectorsUsed in data management, analytics, and technical roles
Search & Comparison IntentFocus on simple typing tasks, entry-level rolesInvolves data entry plus software proficiency, higher skill level

Remote Data Entry Simple Typing typically involves basic data input tasks requiring minimal technical skills, while Remote Data Entry with Advanced Software Skills demands familiarity with specific software tools and more technical knowledge. Both roles are common in various industries, but the latter offers more complexity and potential for higher pay.

What are popular job titles related to Remote Data Entry Simple Typing jobs in San Ramon, CA? For Remote Data Entry Simple Typing jobs in San Ramon, CA, the most frequently searched job titles are:
What job categories do people searching Remote Data Entry Simple Typing jobs in San Ramon, CA look for? The top searched job categories for Remote Data Entry Simple Typing jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Remote Data Entry Simple Typing jobs? Cities near San Ramon, CA with the most Remote Data Entry Simple Typing job openings:
Remote Data Entry Simple Typing jobs near you
Clinical Trial Manager - Contractor

Clinical Trial Manager - Contractor

Arcus Biosciences

Brisbane, CA • On-site, Remote

Contractor

Posted 3 days ago

Job description

Description
Summary
The Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient delivery of clinical trials in a matrix environment. Key accountabilities include assuring successful conduct of clinical studies consistent with applicable regulations, guidelines and procedures, as well as supporting clinical project timelines, contracts, budgets, vendor management, invoicing, accruals, oversight monitoring visits, meeting milestones and deliverables, and internal/external communications. This position is remote or in-house, depending on prior experience. This position will report to a Clinical Operations Manager. Bay Area staff will operate in a hybrid or office based model aligned with Arcus expectations.
Responsibilities
  • Day-to-day management of assigned operational aspects of low to medium complex clinical trials, including but not limited to vendor/ laboratory management, oversight of clinical sites, etc.
  • Obtains and reviews all required essential documents necessary for study/site initiation
  • Maintains/files accurate and timely sponsor/site correspondence and communication. Prepares and presents project progress reports
  • Manages and tracks patient enrollment, site performance and monitoring metrics
  • Performs tasks in accordance with ICH GCP, regulations, the protocol, and company SOPs/Policies
  • Supports the development and review of clinical study plans, presentations or study-related documents
  • Support in the development and design of CRFs, including participating in the EDC and IXRS specification process and UAT on related systems
  • Assists with set-up of central labs and study vendors as required, including liaising with Clinical Program Manager and CRO to ensure site training and timely initiation of clinical study sites
  • Performs in-house review of clinical data listings for completeness and accuracy and escalate issues to the Clinical Program Manager, as needed
  • Works closely with data management lead to perform data cleaning activities with cross-functional team
  • May lead and coordinate protocol deviation review and documentation
  • Manage clinical monitoring activities and the overall site management ensuring compliance with Good Clinical Practices (GCP) and applicable regulations and tracking of site performance metrics
  • May perform accompanied site visits with CRO Site Monitors to ensure correct study procedures according to SOPs and protocol procedures, review of routine regulatory documents/files in compliance with protocol, regulatory requirements, site and CRO SOPs, and study plans, as required
  • Reviews monitoring trip reports and track resolution of all action items
  • Participates in the selection, training, and evaluation of study personnel (vendor, CRO, internal)
  • Assists with providing oversight of CROs and vendors
  • Coordinates with CRO and SMTL in clinical site oversight, data entry timeliness, assists with resolving site issues
  • Assists with set-up and review of clinical TMF
  • Organizes and manages internal team meetings, investigator meetings, and other trial specific meetings, as requested
  • Contributes to development and review of clinical trial documents such as clinical protocol, informed consent form(s), patient facing materials, etc.
  • Provides support in the development and management of vendor scope of work (SOW) per contract, quality, budget, and detailed timelines including investigator and vendor payments, as applicable
  • Recommend and implement innovative ideas to increase efficiency and quality of program management activities
  • Contributes to process and departmental and cross-functional improvement activities

Qualifications
  • Bachelor's degree, preferably in a scientific field
  • 5+ years of related industry experience in the pharmaceutical industry or equivalent, plus 2+ years of trial management experience, preferably in oncology
  • Demonstrates core understanding of clinical trial related terminology and activities
  • Thorough understanding of ICH GCP guidelines and Code of Federation Regulations
  • Understanding of clinical trial processes from study start-up through study closure
  • Ability to establish priorities, sense of urgency and collaborate (interpersonal, relationship management) with the study team, cross functional team members and external partners/vendors
  • Excellent planning and organization skills
  • Self-motivated, assertive, and able to function independently and as part of a team
  • Strong interpersonal and negotiation skills as well as strong verbal and written communication (including presentation of materials to internal teams and external partners)
  • Excellent IT Microsoft skills and experience using clinical trial management web-based systems (i.e. EDC, IRT, CTMS, eTMF, etc.)
  • Ability and willingness to travel 10-20% (domestic and international)
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