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Remote Ucsf Clinical Research Jobs (NOW HIRING)

Tufts Medicine

$26.50 - $35.25/hr

The Clinical Research Coordinator II will support participant recruitment, study operations, data collection, regulatory compliance, and participant retention across clinic-based and remote research ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

... conducts remote and on site monitoring visits such as qualification/pre study visits, site ... Expertise in clinical research operations, including interpretation and implementation of country ...

The Pennsylvania State University

$54K - $78K/yr

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... The Clinical Research Coordinator provides operational oversight for research projects and ...

New

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology - Washington DC ICON is a global healthcare ... Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ...

ICON

Senior Clinical Research Associate

Chicago, IL · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Chicago ICON is a global healthcare ... Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site ...

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Remote Ucsf Clinical Research information

See salary details

$49K

$107.3K

$189K

How much do remote ucsf clinical research jobs pay per year?

As of Aug 7, 2026, the average yearly pay for remote ucsf clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is a remote UCSF clinical research job?

A remote UCSF clinical research job involves supporting or conducting clinical studies at the University of California, San Francisco (UCSF) while working from a location outside of the university, often from home. These roles can include study coordination, data collection and analysis, regulatory support, and patient communication, all performed virtually. Remote positions allow for flexible work arrangements and are ideal for individuals who have strong organizational and communication skills, as well as experience in research or healthcare. Employees in these roles still adhere to UCSF’s high standards for scientific integrity and patient privacy, and may use digital tools to collaborate with research teams.

What are the key skills and qualifications needed to thrive as a remote UCSF Clinical Research professional?

To excel in Remote UCSF Clinical Research, you need a background in life sciences or a related field, experience with clinical trial protocols, and often a relevant certification such as CCRC or SOCRA. Familiarity with electronic data capture (EDC) systems, IRB processes, and remote monitoring tools is crucial. Strong organizational skills, attention to detail, and effective communication are vital soft skills for managing remote collaboration and complex documentation. These abilities ensure accurate data collection, regulatory compliance, and successful execution of clinical studies in a remote setting.

What is the difference between Remote Ucsf Clinical Research vs Remote Ucsf Clinical Research Coordinator?

AspectRemote Ucsf Clinical ResearchRemote Ucsf Clinical Research Coordinator
CredentialsBachelor's degree, research experienceBachelor's degree, research experience, often certification
Work EnvironmentRemote, administrative and data management tasksRemote, participant interaction, study coordination
Employer & IndustryUCSF, healthcare researchUCSF, healthcare research

Remote UCSF Clinical Research roles focus on data management and administrative tasks, while Remote UCSF Clinical Research Coordinators handle participant interactions and study coordination. Both roles require research experience and are integral to UCSF's healthcare research efforts, but they differ in daily responsibilities and certification needs.

How does working remotely as a UCSF Clinical Research professional affect team collaboration and communication?

Working remotely in a UCSF Clinical Research role typically means collaborating with multidisciplinary teams—including investigators, coordinators, and data managers—through digital platforms like email, Zoom, and project management tools. While remote work offers flexibility, it also requires proactive communication and strong organizational skills to ensure all regulatory, data collection, and study coordination tasks are aligned. Regular virtual meetings and shared documentation are critical for keeping everyone updated and maintaining compliance. Candidates should be comfortable with digital communication tools and self-motivation to thrive in this environment.
More about Remote Ucsf Clinical Research jobs
What cities are hiring for Remote Ucsf Clinical Research jobs? Cities with the most Remote Ucsf Clinical Research job openings:
What are the most commonly searched types of Ucsf Clinical Research jobs? The most popular types of Ucsf Clinical Research jobs are:
What states have the most Remote Ucsf Clinical Research jobs? States with the most job openings for Remote Ucsf Clinical Research jobs include:
What job categories do people searching Remote Ucsf Clinical Research jobs look for? The top searched job categories for Remote Ucsf Clinical Research jobs are:
Remote Ucsf Clinical Research jobs near you
Infographic showing various Remote Ucsf Clinical Research job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, 15% Part Time, 5% Temporary, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Senior Clinical Research Associate

Icon plc

Blue Bell, PA • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 19 days ago

Job description

Senior CRA/ CRA II

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.


We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

  • Collaborating with investigators and site staff to facilitate smooth study conduct.

  • Performing data review and resolution of queries to maintain high-quality clinical data.

  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports


Your profile

  • Bachelor's degree in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role

  • Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

  • Strong organizational and communication skills, with attention to detail.

  • Ability to work independently and collaboratively in a fast-paced environment.

  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license

#LI-ZH1

#LI-REMOTE


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 requesthere.

Are you a current ICON Employee? Please click here to apply

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