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Clinical Research Biotech Remote Jobs (NOW HIRING)

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

Ōura

Clinical Research Coordinator

$24.75 - $33/hr

We are looking for a Clinical Research Coordinator to join our Clinical Research Operations team ... This is a remote US role, with a preference for candidates based in San Francisco, Boston, or San ...

Essentia Health

Clinical Research Assistant

Duluth, MN · On-site +1

$18.69 - $27.85/hr

Experience in oncology, clinical research, academic research or similar area. Over 1 year computer ... None FTE: 1 Possible Remote/Hybrid Option: Shift Rotation: Day Rotation (United States of America ...

Hanger, Inc.

Director of Clinical Research

$140K - $150K/yr

The Director of Clinical Research will serve within Hanger's Department of Clinical and Scientific ... Remote: Pay range of $140,000- $150,000 + bonus + benefits. This pay range is posted to comply with ...

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Clinical Research Biotech Remote information

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$49K

$107.3K

$189K

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

As of Jul 21, 2026, the average yearly pay for clinical research biotech remote 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 does a Clinical Research Biotech Remote professional do?

A Clinical Research Biotech Remote professional manages and oversees clinical trials and research studies for biotech companies while working from a remote location. Their responsibilities typically include coordinating study protocols, ensuring regulatory compliance, collecting and analyzing data, and collaborating with investigators and other stakeholders virtually. By working remotely, these professionals use digital tools to monitor trial progress and maintain communication with research teams, sponsors, and regulatory bodies. Their work plays a crucial role in advancing new biotech therapies and medical technologies.

What is the difference between Clinical Research Biotech Remote vs Clinical Research Associate?

AspectClinical Research Biotech RemoteClinical Research Associate
CredentialsBachelor's degree in life sciences; certifications like CCRP or RACBachelor's degree in life sciences; often required certifications like CCRP
Work EnvironmentRemote, flexible locationTypically on-site or travel-based, but remote options are increasing
Employer & IndustryBiotech companies, pharmaceutical firms, CROsPharmaceutical companies, CROs, biotech firms
Job FocusSupporting clinical trials remotely, data management, regulatory complianceMonitoring clinical trials, site visits, ensuring protocol adherence

While both roles involve clinical trial support, Clinical Research Biotech Remote focuses on remote data and regulatory tasks within biotech companies, whereas Clinical Research Associate typically involves on-site monitoring and site management. The remote role offers flexibility, while the CRA role emphasizes direct site interaction.

What are the key skills and qualifications needed to thrive as a Clinical Research Biotech professional in a remote setting, and why are they important?

To thrive as a Clinical Research Biotech professional working remotely, you typically need a background in life sciences, experience in clinical research methodologies, and familiarity with regulatory requirements such as GCP and FDA guidelines. Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and remote collaboration tools is essential. Strong organizational skills, self-motivation, and effective virtual communication set top performers apart in remote environments. These abilities are crucial for ensuring regulatory compliance, maintaining data integrity, and collaborating efficiently across dispersed teams.

How does a Clinical Research Biotech professional collaborate with cross-functional teams in a remote setting?

In a remote Clinical Research Biotech role, professionals frequently collaborate with cross-functional teams, including clinical operations, regulatory affairs, data management, and biostatistics. Communication typically occurs via video conferences, collaborative platforms, and shared digital workspaces. Successful candidates should be comfortable navigating time zone differences and proactively sharing updates to ensure project milestones are met. Building strong virtual relationships and maintaining transparency are key to overcoming challenges and ensuring seamless trial execution.
More about Clinical Research Biotech Remote jobs
What cities are hiring for Clinical Research Biotech Remote jobs? Cities with the most Clinical Research Biotech Remote job openings:
What states have the most Clinical Research Biotech Remote jobs? States with the most job openings for Clinical Research Biotech Remote jobs include:
What job categories do people searching Clinical Research Biotech Remote jobs look for? The top searched job categories for Clinical Research Biotech Remote jobs are:
Clinical Research Biotech Remote jobs near you
Infographic showing various Clinical Research Biotech Remote job openings in the United States as of July 2026, with employment types broken down into 8% Internship, 76% Full Time, 8% Part Time, and 8% 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, Field Monitor

Senior Clinical Research Associate, Field Monitor

ImmunityBio, Inc.

Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago

Job description

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
• ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
• Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
• Work with a collaborative team with the ability to work across different areas of the company.
• Ability to join a growing company with professional development opportunities.
Position Summary
Senior Clinical Research Associate will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies by providing training, protocol interpretation, document collection and review and overall clinical trial support.
Essential Functions
  • Develop, review and update study-related training materials and documents including: site initiation training slides, informed consent form templates, procedures manuals, laboratory and pharmacy manuals
  • Interpret medical and scientific intent of assigned study protocols and study procedures, logistics, risks to research subjects and safety, data evaluation methods etc.
  • Communicate scientific rationale for assigned studies to team members and clinical sites
  • Serve as Subject Matter Expert for clinical sites including providing guidance on protocol interpretation and eligibility requirements
  • Create/edit, distribute and collect site feasibility questionnaires
  • Oversee and support collection of essential documents during study start-up
  • Collect study and site metrics and maintain study trackers, as needed
  • Participate in case report form (CRF) data review and review of source documents, work with sites to resolve data queries as needed
  • Communicate regularly with field and in-house Clinical Research Associates (CRAs) to provide information before and after site visits
  • Partner with field CRAs to resolve issues identified during site visits
  • Work with Supply Chain to ensure sites maintain sufficient investigational product (IP) to properly conduct the trial as well as resolve IP temperature monitoring excursions and train or assist sites with corrective actions
  • Train vendors, investigators, and study coordinators on study requirements and provide guidance on site issues
  • Clinical specimen log review, coordinating shipment of specimens to the sponsor or contracted vendor
  • Conduct remote monitoring tasks including reconciliation of site investigational product accountability, as needed
  • Provide mentorship and training to newly hired research staff.
  • Performs other duties as assigned.

Education & Experience
  • Bachelor's degree in a clinical research, science, or health-related field with 6 years of clinical trial experience within a pharmaceutical, biotechnology, CRO, and/or healthcare setting required
  • Minimum 4 years of on-site monitoring experience required

Knowledge, Skills, & Abilities
  • Proficiency in MS Word, Excel, PowerPoint, Outlook, Adobe
  • Excellent written/oral communication skills as well as strong organizational and multi-tasking skills
  • Strong organizational and multi-tasking skills
  • Understand the job-specific system, processes as defined by the company's SOPs, and adhere to the requirements listed in those documents. If any of the procedure or process requirements are unclear or ambiguous, it is the responsibility of the employee to notify his/her supervisor or manager.
  • Maintain corporate confidentiality at all times
  • Ability to set priorities and independent decision making
  • Ability to work independently as well as in teams
  • Ability to discover issues, provides solutions and provides guidance to in-house team on how to address issues
  • Strong oral and written communication skills
  • Outgoing and confident demeanor
  • Independent thinker and persuasive communicator
  • Detail oriented, with solid organization and time management skills
  • Completes projects with reliability and minimal guidance
  • Knowledge of drug development process
  • Computer literacy: EDC, eTMF, CTMS, etc.
  • Working knowledge of ICH E6, and the Code of Federal Regulations

Working Environment / Physical Environment
  • Must be able to travel up to 75% of the time based on study requirements
  • Remote with ability to work flexible hours for various time zones

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.
National Market (all markets unless identified as Premium)
$128,000 (entry-level qualifications) to $136,000 (highly experienced) annually
Premium Market (Premium markets include Los Angeles, San Diego, San Francisco, New York City, Chicago, & Boston)
$133,000 (entry-level qualifications) to $140,000 (highly experienced) annually
The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.
ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO) includes: 11 Holidays • Exempt Employees are eligible for Unlimited PTO • Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day • We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.
At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

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