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From Home Icon Clinical Trial Jobs (NOW HIRING)

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... days from home. Employment with ICON is contingent upon having the legal right to work in the ...

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... days from home. Employment with ICON is contingent upon having the legal right to work in the ...

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... days from home. Employment with ICON is contingent upon having the legal right to work in the ...

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... days from home. Employment with ICON is contingent upon having the legal right to work in the ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liasion - Immunology ICON is a global healthcare intelligence and clinical research ... Accountable for the full spectrum of investigator engagement from identification and qualification ...

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation ... Accountable for the full spectrum of investigator engagement from identification and qualification ...

Clinical Trial Liaison

Blue Bell, PA · On-site +1

$110K - $138K/yr

Clinical Trial Liaison - Mid- Atlantic ICON is a global healthcare intelligence and clinical ... Accountable for the full spectrum of investigator engagement from identification and qualification ...

Clinical Trial Liaison - Mid- Atlantic ICON is a global healthcare intelligence and clinical ... Accountable for the full spectrum of investigator engagement from identification and qualification ...

Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

Clinical Trial Liasion - Immunology ICON is a global healthcare intelligence and clinical research ... Accountable for the full spectrum of investigator engagement from identification and qualification ...

Clinical Trial Liaison

Blue Bell, PA · On-site

$110K - $138K/yr

Clinical Trial Liaison ICON is a global healthcare intelligence and clinical research organisation ... Accountable for the full spectrum of investigator engagement from identification and qualification ...

Clinical Development Trial Lead ICON is a global healthcare intelligence and clinical research ... Be accountable for trial/regional enrollment strategy and execution starting from country ...

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From Home Icon Clinical Trial information

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How much do from home icon clinical trial jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for from home icon clinical trial in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is the difference between From Home Icon Clinical Trial vs Clinical Research Coordinator?

AspectFrom Home Icon Clinical TrialClinical Research Coordinator
CredentialsTypically requires a background in health sciences, nursing, or related fields; certifications like CCRP are commonRequires similar health science background; certifications like CCRP or CRC are often preferred
Work EnvironmentPrimarily remote, managing trial data and communication onlineUsually on-site at clinics or hospitals, with some remote tasks
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for remote trial managementCommonly employed by hospitals, research centers, and clinical trial sites

While both roles involve clinical trial work and require health science credentials, From Home Icon Clinical Trial positions are primarily remote, focusing on data management and communication. Clinical Research Coordinators often work on-site, coordinating patient visits and trial procedures. The choice depends on your preference for remote work versus on-site responsibilities.

What cities are hiring for From Home Icon Clinical Trial jobs?

Cities with the most From Home Icon Clinical Trial job openings:

What are the most commonly searched types of Icon Clinical Trial jobs?

The most popular types of Icon Clinical Trial jobs are:

What states have the most From Home Icon Clinical Trial jobs?

States with the most job openings for From Home Icon Clinical Trial jobs include:

Clinical Trial Assistant

ICON

San Francisco, CA • On-site

$56K - $70K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago


Job description

Clinical Trial Assistant (San Francisco, CA)
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
What you will be doing:
The Clinical Trial Assistant is a member of the clinical trial team supporting delivery of clinical studies within the sponsor. The CTA will support the study team to ensure the operational deliveries are executed then the expected timeline, approved budget, and at high quality from protocol development through study setup, maintenance, close out and study archiving.
  • The CTA supports the study team in delegated activities and provides technical, administrative and logistical support to ensure efficient execution of clinical trials in line with ICH/GCP sponsor SOP's and regulatory regulations.
  • Lead the setup of electronic Trial Master File (eTMF) system and clinical trial management (CTMS). Ensure information is updated during the study per ICH/GCP and sponsor SOP's
  • Create and maintain communication platforms (i.e. MS Teams, SPOL, group e-mail list) for the study team
  • Control systems access for assigned studies but not limited to IxRS, EDC, CT's, and eTMF
  • Support clinical trial registration and disclosure on websites per applicable regulatory requirements
  • Responsible for overall TMF status. Guide study team members on the eTMF/paper TMF document transfer and archival. Lead the quality check (QC) per the TMF plan. Help draft TMF plan
  • Facilitate finance related activities such as sign off, IO and PO setup, processing invoices, track accruals and budget for maintenance and reconciliation for sites and third-party vendors
  • Support oversight of monitoring visit report review. Activities include updating MVR trackers and overseeing MVR review metrics
  • May support data oversight and reconciliation efforts vendor systems, SAEs, protocol deviations and more as needed per study
  • Coordination and tracking of clinical supplies
  • Coordinate and arrange internal and external meetings, including but not to study team meetings, vendor defense meetings, investigator meetings, and committee review meeting take meeting minutes as needed.
  • Compile and maintain the clinical trial related lists and logs, including but not limited to study document version tracker, decision risk log, contact list, Q&A log, vendor list, and specific training log.
  • Draft and distribute newsletters communications Asia materials to internal and external stakeholders
  • Complete delegated tasks during audit and inspection by regulatory authorities

What you need to have:
  • High school or GED with four years relevant experience. Bachelor's degree or above (Life Sciences preferred) or certification in a related health profession (i.e. nursing, medical or laboratory technology) from an accredited institution is preferred.
  • At least 1 year experience as a CTA, CRC, or other role in clinical trials.
  • Oncology experience a huge plus!
  • Proven organizational and presentation skills
  • Ability to manage multiple tasks with meticulous attention to detail
  • Quick learner and team player
  • Excellent written and verbal communication skills
  • Computer proficiency in Microsoft Word, Excel, PowerPoint and Outlook
  • Good knowledge of the ICH/GCP
  • Position is on site 3-4 days a week at client office in South San Francisco, CA and days from home.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Salary Range
$56,704.00-$70,880.00
Are you a current ICON Employee? Please click here to apply