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Remote Ucsf Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

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Remote Ucsf Clinical Research information

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$49K

$107.3K

$189K

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

As of Aug 11, 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:
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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 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Financial Analyst (Remote)

The START Center for Cancer Research

Remote

$70K - $80K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

The START Center for Cancer Research ("START") is the world's largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access" to cutting edge trials throughout the United States and Europe.
We are seeking a Clinical Research Financial Analyst who will be
responsible for researching and mapping clinical research financials via reporting from START's CTMS system. This role will assist in identification and financial reconciliation of expenses from all participating sites and assist START Accounting in billing. This position plays a critical role in ensure that START can fully capture revenue for services provided, in particular for patient visit variations which require specialized coding and tracking to ensure payment by the clinical trial sponsor.
The annual base salary for this remote role is $65,000 - $80,000. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.
Work Schedule: M-F 8:00AM-5:00PM
Location: Remote
Essential Responsibilities:
  • Research and map clinical research financials via Advarra Visit Variation Report to contract pricing.
  • Collaborate with Sponsors and CROs to organize direct invoicing in applicable scenarios.
  • Work with START Accounting to properly identify direct invoicing scenarios and indicate on necessary trackers.
  • Participate in larger reporting projects that assist in identification of rogue or potential erroneous trial expenses.
  • Attend Revenue Cycle task meetings with Leadership and Study Teams in order to align with CTMS visions and changing landscape.
  • Work with Clinical site operations teammates and systems (ARIA) to provide necessary detail for sponsor billing and payment.
  • Assist in streamlining the mapping and reconciliation process to assist with company growth and scaling.

Required Education and Experience:
  • Bachelor's degree in financial or business administration field (Accounting, Finance, Business Administration, or similar field).
  • Minimum of one year of CTMS experience, or equal experience of education and knowledge.
  • Clinical Trial Management System (OnCore specific) experience.
  • MS Office Excel and other MS Office programs.

Preferred Education and Experience:
  • Bachelor's degree in financial or business administration field (Accounting, Finance, Business Administration, or similar field).
  • Minimum of one year of CTMS experience, or equal experience of education and knowledge.
  • Clinical Trial Management System (OnCore specific) experience.
  • MS Office Excel and other MS Office programs.

Best-in-Class Benefits and Perks
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package-based on experience-along with comprehensive benefits designed to support you both personally and professionally:
  • 401(k) retirement savings plan with employer match
  • Eligibility for an annual performance bonus, based on role and company results
  • Generous paid time off and paid holidays
  • Comprehensive medical, dental, and vision coverage and optional insurance options
  • Company paid life and disability insurance for added financial protection
  • Employee Assistance Program (EAP) providing confidential, no -cost support for you and your family from day one
  • Flexible FSA and HSA plans to support your financial wellness
  • Commitment to a supportive environment that values balance, wellbeing, and flexibility
  • We're committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you'll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world's largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of "Hope Through Access".
Learn more atSTARTresearch.com.
Ready to be part of a team changing the future of cancer treatment?
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

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