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From Home Clinical Trial Data Transparency Jobs (NOW HIRING)

City of Hope

Sr Clinical Trials Data Coord

Duarte, CA · On-site

Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout. * Ensure data accuracy, completeness ...

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Clinical Trial Manager

Raleigh, NC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...

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Clinical Trial Manager

Houston, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

This role is pivotal in ensuring key project deliverables, primarily from CROs and vendors, are met ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...

ICON

Clinical Trial Manager

Raleigh, NC · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Perform data verification and reconciliation of study trackers against EDC, CTMS, and other ... Working knowledge of the clinical trial lifecycle, from protocol development through study close ...

C4 Therapeutics Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

Lead the execution of the day-to-day operational aspects of clinical study(ies) from protocol ... Perform and contribute to clinical data cleaning as part of cross-functional data review team.

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Ensure the quality of data submitted from assigned study tasks and timely data submission ...

Icon plc

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical ... Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top ...

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

... from the assigned Study Lead. The CTA plays a key role in study start-up, ongoing trial execution ... Support ongoing maintenance of the Clinical Trial Management System (CTMS), ensuring data accuracy ...

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As of Aug 13, 2026, the average hourly pay for from home clinical trial data transparency in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.
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Infographic showing various From Home Clinical Trial Data Transparency job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 22% Part Time, and 4% Contract. Highlights an 79% Physical, 1% Hybrid, and 20% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Sr Clinical Trials Data Coord

City of Hope

Duarte, CA • On-site

Full-time

Posted 16 days ago

City Of Hope rating

8.4

Company rating: 8.4 out of 10

Based on 89 frontline employees who took The Breakroom Quiz

23rd of 887 rated healthcare providers

Job description

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. 

The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and query resolution to ensure accurate, reliable, and compliant research data. The role involves interpreting research protocols, reviewing medical records, resolving discrepancies, and maintaining study visits and financial triggers within the Clinical Trial Management System (CTMS) aligned with Electronic Data Capture (EDC) systems. Working closely with physicians, clinical coordinators, and research teams, the coordinator ensures timely data reporting, supports adverse event data collection, and contributes to study monitoring and regulatory compliance. Additionally, the role includes performing peer data reviews, assisting in the development of data management plans and workflows, and providing training and guidance to research data staff to maintain high-quality clinical trial data and efficient research operations.

As a successful candidate, you will: 

  • Enter and manage clinical trial data in EMR, CTMS (OnCore), and EDC systems within required timelines while supporting studies from start-up through closeout.
  • Ensure data accuracy, completeness, and compliance through quality checks, data cleaning, and timely resolution of queries.
  • Maintain regulatory compliance with FDA, ICH-GCP, ALCOA , HIPAA, and other applicable guidelines for clinical research data management.
  • Collaborate with sponsors, physicians, and clinical coordinators to resolve protocol issues, data discrepancies, and ensure proper documentation.
  • Manage adverse event documentation and classification using standard dictionaries such as MedDRA, CTCAE, and WHO-DDE, including SAE follow-up and query resolution.
  • Maintain study calendars, financial triggers, and data completion tracking in CTMS to support billing and study financial management.
  • Support monitoring visits, study initiation visits, audits, and inspection readiness, ensuring data quality and completeness.
  • Contribute to data management improvements by assisting with EDC builds, creating data standards, preparing reports, participating in CAPA and process improvement initiatives, and mentoring peers.
 
Qualifications - External
 
Qualifications - External

Your qualifications should include: 

Minimum Education

 Bachelor's degree in Science, Health, or a related field from an accredited university, or equivalent relevant work experience.

Minimum Experience: Minimum of 5-7 years of clinical research or related experience.

Required Certifications:

 Completion of Good Clinical Practice (GCP) training within 1 month of employment.

 Completion of Human Subjects Protection (HSP) training within 1 month of employment.

Ability to obtain SOCRA or ACRP certification within 2 years of employment.
Systems Knowledge: Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory systems.

City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

City of Hope is an equal opportunity employer.  To learn more about our commitment to diversity, equity, and inclusion, please click here.

To learn more about our Comprehensive Benefits, please CLICK HERE.

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About City of Hope

Sourced by ZipRecruiter

City of Hope is an independent biomedical research and treatment organization for cancer, diabetes and other life-threatening diseases. Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hopes translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope, a subsidiary launched in 2019 serves employers and their health care partners by providing access to City of Hopes specialized cancer expertise. City of Hope is ranked among the nations Best Hospitals in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.

Industry

Hospitals

Company size

1,001 - 5,000 Employees

Headquarters location

Duarte, CA, US

Year founded

1913

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