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Full Time Remote Clinical Trials Jobs (NOW HIRING)

Manager, Clinical Trials

San Carlos, CA · Remote

$115K - $144K/yr

The Clinical Trial Manager should have experience in managing all aspects of the trials ... Remote USA $115,800--$144,700 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA ...

New

THE ROLE We are seeking a full-time, fully benefited Vitalief employee to serve as a Clinical Trials Coverage Analyst in a fully remote capacity, supporting a leading academic clinical research ...

THE ROLE We are seeking a full-time, fully benefited Vitalief employee to serve as a Clinical Trials Coverage Analyst in a fully remote capacity, supporting a leading academic clinical research ...

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Clinical Research Study Coordinator Albuquerque Clinical Trials (ACT) seeks an experienced, full-time Clinical Research Study Coordinator. The ideal candidate is passionate about research and helping ...

New

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Clinical Research Study Coordinator Albuquerque Clinical Trials (ACT) seeks an experienced, full-time Clinical Research Study Coordinator. The ideal candidate is passionate about research and helping ...

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Remote Essential Functions * Provide scientific leadership for the planning, design, and implementation of complex Phase II-III clinical trials, ensuring adherence to regulatory, ethical, and ...

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Clinical Research Study Coordinator Albuquerque Clinical Trials (ACT) seeks an experienced, full-time Clinical Research Study Coordinator. The ideal candidate is passionate about research and helping ...

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Clinical Trials Contracts Manager

New Brunswick, NJ · Remote

$91K - $121K/yr

THE ROLE We are seeking a full-time, fully benefited Clinical Trials Contracts Manager to join Vitalief in a fully remote position supporting our client, a leading academic clinical research center ...

Clinical Trials Contracts Manager

New Brunswick, NJ · On-site +1

$91K - $122K/yr

THE ROLE We are seeking a full-time, fully benefited Clinical Trials Contracts Manager to join Vitalief in a fully remote position supporting our client, a leading academic clinical research center ...

Monitoring will be performed through a combination of remote data review and onsite monitoring visits; therefore, a willingness and ability to travel occasionally is required. The Clinical Trials ...

Project Specialist

$60K - $76K/yr

At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO ... This role provides full-time support to our Project Managers, contributing directly to the delivery ...

Remote Work Practices: Cogstate is a virtual first company. Cogstate employees can work from ... We also offer free vision insurance for all full-time employees. * Short-Term & Long Term ...

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Full Time Remote Clinical Trials information

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How much do full time remote clinical trials jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for full time remote clinical trials 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.

What is the difference between Full Time Remote Clinical Trials vs Full Time Remote Clinical Research Coordinators?

AspectFull Time Remote Clinical TrialsFull Time Remote Clinical Research Coordinators
CredentialsTypically requires a degree in life sciences, nursing, or related fields; certifications like CCRP are commonSimilar credentials, often with certifications like CCRP or CRC
Work EnvironmentConducts or oversees clinical trials remotely, often collaborating with sites and sponsorsCoordinates trial activities, manages data, and communicates with sites remotely
Industry UsageUsed by pharmaceutical companies, CROs, and research institutionsCommonly employed by research organizations and sponsors for trial management

Both roles involve remote work in clinical research, requiring similar credentials and industry usage. Full Time Remote Clinical Trials focus on overseeing or conducting entire trials, while Clinical Research Coordinators handle day-to-day trial coordination and data management. Understanding these differences helps job seekers find the right fit in the remote clinical research field.

More about Full Time Remote Clinical Trials jobs
What cities are hiring for Full Time Remote Clinical Trials jobs? Cities with the most Full Time Remote Clinical Trials job openings:
What are the most commonly searched types of Remote Clinical Trials jobs? The most popular types of Remote Clinical Trials jobs are:
What states have the most Full Time Remote Clinical Trials jobs? States with the most job openings for Full Time Remote Clinical Trials jobs include:
What job categories do people searching Full Time Remote Clinical Trials jobs look for? The top searched job categories for Full Time Remote Clinical Trials jobs are:

Manager, Clinical Trials

Natera

San Carlos, CA • Remote

$115K - $144K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday


Natera rating

7.7

Company rating: 7.7 out of 10

Based on 35 frontline employees who took The Breakroom Quiz

47th of 103 rated laboratories


Job description

POSITION SUMMARY:

The Manager, Clinical Trials will be responsible for managing all aspects of clinical trials from start-up through close-out. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, and is expected to provide functional expertise to ensure that study timelines, costs and quality metrics are met and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements.

PRIMARY RESPONSIBILITIES:

  • Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met

  • Responsible for selection of vendors/CROs and provide effective ongoing management to vendors/CROs working on the project to ensure compliance and execution of project deliverables within the approved budget, study timeline, and study protocol. Works closely with investigative site personnel, CROs, and other study vendors

  • Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites

  • Lead study-related activities such as protocol and informed consent preparation, investigator selection, study training material development and delivery, monitoring plans development and execution, CRFs, design and completion, TMF maintenance, protocol amendment and clinical report preparation, as required

  • Collaborate with Clinical Data Management group to ensure correct CRFs content is collected, prepare comprehensive completion guidelines, and design effective data listings and study reports

  • Train CROs, vendors, investigators and study coordinators on implementation of study protocol

  • Hire, train, manage and oversee Clinical trial staff, and serve as a resource for others within the company for clinical trials management expertise

  • Monitor and track clinical trial progress and provide status update to stakeholders

  • Support sample management and prospective sample testing for studies where Natera functions as a central testing facility

  • Partner with other research and development groups to create a culture of mutual respect and focus on delivery of high-quality project results

  • Develop Clinical Department SOPs and participate in audits as needed

  • This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job.

  • Employee must provide records of current training or complete training relating to HIPAA/PHI privacy, Human Subjects Protection, and GCP training.

  • Must maintain a current status on Natera training requirements including General Policies and Procedure Compliance and security training.

  • Employee must pass post offer criminal background check

QUALIFICATIONS:

  • Bachelor's degree in life sciences, or other relevant discipline required, Advanced degree preferred.

  • 8 years of clinical research experience, including at least 4 years of experience in managing clinical trials as a leading role.

  • 4-7 years of experience in supporting clinical trials in a regulated environment .

  • Experience in managing CROs is preferred.

KNOWLEDGE, SKILLS, AND ABILITIES:

  • Knowledge and understanding of Clinical Trial SOPs, FDA Regulations, and ICH-GCPs governing the conduct of clinical trials

  • Demonstrated analytical skills and ability to identify problems and solutions independently

  • Ability to collaborate with the study team, cross functional team members and external collaborators

  • Proficiency in MS Word, Excel and PowerPoint

  • Good organization and planning skills

  • Strong interpersonal skills and communication skills (both written and oral)

  • Strong leadership skills, self-motivated, adaptable to a dynamic and fast paced environment

  • Must have excellent organizational and time management skills.

  • Ability to prioritize and handle multiple tasks and projects in a fast-paced environment

The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.
Remote USA
$115,800—$144,700 USD

OUR OPPORTUNITY

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

For more information, visit www.natera.com.

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

If you are based in California, we encourage you to read this important information for California residents.

Link: https://www.natera.com/notice-of-data-collection-california-residents/

Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.

For more information:
- BBB announcement on job scams
- FBI Cyber Crime resource page


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