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Remote Clinical Trial Associate Jobs (NOW HIRING)

Clinical Trial Manager

San Francisco, CA ยท On-site +1

$145K - $165K/yr

About the Job We are hiring a Clinical Trial Manager to support the successful execution of our ... as a remote work day * Ability to travel as needed (10% - 15%) * Qualified candidates must be ...

Close collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline ...

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ... Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study ...

Clinical Operations Associate (Pool)

CA ยท Remote

$70K - $80K/yr

We are experts in clinical trial operations with a focus on Clinical Trial Management, CRO/Vendor ... Clinical Operations Associate: $70,304 - 80,000 annually + benefits package and annual performance ...

Clinical Trial Manager

Waltham, MA ยท On-site +1

$136K - $160K/yr

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Clinical Trial Manager

Newark, CA ยท On-site +1

$136K - $160K/yr

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Clinical Trial Manager

Newark, CA ยท On-site +1

$136K - $160K/yr

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Clinical Trial Manager

Waltham, MA ยท On-site +1

$136K - $160K/yr

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of ... Remote work considered; preference for candidates able to attend the office weekly (Newark or ...

Sr Clinical Trial Manager ICON is a global healthcare intelligence and clinical research ... Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * Timely Study ...

SummaryThe Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

Remote, US East Coast Job Type: Full-Time Reports To: Head of Country Delivery Internal Team Title: Clinical Trial Manager JOIN US AT CIVIA HEALTH Civia Health operates a nextgeneration SMO model ...

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Remote Clinical Trial Associate information

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How much do remote clinical trial associate jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for remote clinical trial associate in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What does a Remote Clinical Trial Associate do?

A Remote Clinical Trial Associate (CTA) supports the planning, execution, and management of clinical trials from a remote location. Their responsibilities include handling documentation, assisting with regulatory submissions, maintaining trial records, and coordinating communication between trial sites, sponsors, and regulatory bodies. Remote CTAs play a crucial role in ensuring that trials are conducted according to protocols, timelines, and regulatory requirements, all while working offsite. This allows for greater flexibility and can improve efficiency in clinical research processes.

Which is better, CRA or CRC?

A Clinical Research Associate (CRA) typically oversees multiple clinical trials, monitors site compliance, and ensures data quality, often working remotely or traveling to sites. A Clinical Research Coordinator (CRC) manages daily trial activities at a specific site, handles patient interactions, and maintains study documentation. Both roles are essential, with CRAs focusing on oversight and CRCs on site management; the choice depends on preferred work environment and career goals.

What are the key skills and qualifications needed to thrive as a Remote Clinical Trial Associate, and why are they important?

To thrive as a Remote Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and typically a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) certification are commonly required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing study documentation and collaborating with remote teams. These competencies ensure trials are conducted efficiently, compliantly, and with high data integrity in a virtual environment.

Is CRA an entry-level job?

A Clinical Trial Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, understanding of Good Clinical Practice (GCP), and sometimes relevant certifications. Entry-level roles in clinical research may include Clinical Research Coordinator or Clinical Research Assistant, with CRAs often advancing from these positions after gaining experience. However, some companies offer junior or trainee CRA roles for candidates with limited experience who demonstrate strong organizational and communication skills.

What are some common challenges faced by Remote Clinical Trial Associates, and how can they be managed?

Remote Clinical Trial Associates often encounter challenges such as maintaining consistent communication with on-site teams, managing multiple studies across different time zones, and ensuring accurate documentation while working virtually. These can be managed by leveraging robust digital communication tools, setting clear expectations for updates, and staying organized with project management software. Proactively building relationships with colleagues and participating in regular virtual meetings also helps ensure alignment and smooth coordination throughout the trial process.

Is a clinical trial associate a good career?

A clinical trial associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trials to ensure compliance and data integrity. It offers opportunities for career growth, requires attention to detail, and often involves working with specialized software and regulatory guidelines. The role can be stable and rewarding for those interested in medical research and patient safety.

Can a clinical research associate work remotely?

Yes, many clinical research associates (CRAs) can work remotely, especially with the increased use of electronic data capture and remote monitoring tools. Remote work allows CRAs to oversee trial sites, review data, and communicate with teams virtually, though some in-person site visits may still be required depending on the study and employer policies.
More about Remote Clinical Trial Associate jobs
What cities are hiring for Remote Clinical Trial Associate jobs? Cities with the most Remote Clinical Trial Associate job openings:
What are the most commonly searched types of Remote Clinical Trial jobs? The most popular types of Remote Clinical Trial jobs are:
What states have the most Remote Clinical Trial Associate jobs? States with the most job openings for Remote Clinical Trial Associate jobs include:
Infographic showing various Remote Clinical Trial Associate job openings in the United States as of June 2026, with employment types broken down into 7% Full Time, and 93% Part Time. Highlights an 70% Physical, 6% Hybrid, and 24% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
Clinical Trial Manager

Clinical Trial Manager

Ossium Health

San Francisco, CA โ€ข On-site, Remote

$145K - $165K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Job description

About the Job

We are hiring a Clinical Trial Manager to support the successful execution of our clinical trials and operations. In this role, you'll take ownership of the day-to-day tactical management of ongoing studies, ensuring seamless trial implementation and monitoring.

You'll play a key role in launching our PRESERVE II clinical trial, the long-term follow-up of PRESERVE I, and our HOPE expanded access program. This position is ideal for someone who thrives in a hands-on, fast-paced environment-someone eager to collaborate across teams and coordinate with internal partners, CROs, and external vendors to deliver excellence in every aspect of our trials.
This role reports to the Senior Director, Clinical Operations.

Required Qualifications
  • Degree in Life Sciences & industry-sponsored clinical trial experience:ย 
    • BS & 3+ years
    • MS/MPH & 1+ years
  • Experience with or managing CROs; either from within a CRO in a major role, or from a sponsor-side biotech or pharmaceutical company at the Clinical Trial Manager or Clinical Project Manager level
  • Strong written and verbal communication skills, with the ability to share complex information clearly and effectively across teams and stakeholders
  • Exceptional organizational and time management abilities, with comfort operating in a fast-moving, dynamic startup environment
  • Proven capacity to manage multiple priorities simultaneously, maintaining accuracy and attention to detail
  • A collaborative, execution-oriented mindset with the ability to build alignment and drive progress across cross-functional teams
  • This position is based in our San Francisco office; we maintain a hybrid schedule of Monday - Thursday in the office, with Friday as a remote work day
  • Ability to travel as needed (10% - 15%)
  • Qualified candidates must be legally authorized to be employed in the United States; Ossium is unable to provide sponsorship for employment visa status (eg, H-1B or TN status) for this position, either now or in the future
Preferred Qualifications
  • CRA/site coordinator experience
  • Trial experiences in full life cycle of clinical trial
  • Experience in cell therapyย 
  • Experience in rare disease; hematologic malignancies (specifically bone marrow transplant)
Key Responsibilities
  • Serve as the primary liaison with the CRO supporting PRESERVE II study activities, ensuring alignment on timelines and deliverables
  • Review and contribute clinical operations input to key study documents including protocols, investigator brochures, regulatory submissions, clinical study reports, and operational plans developed by CRO partners
  • Oversee site feasibility and capability assessments in close collaboration with the CRO and cross-functional teams
  • Support additional clinical programs and studies as assigned, working closely with the Senior Director, Clinical Operations to meet strategic and operational objectives
  • Partner with cross-functional groups, including Transplant Operations, Regulatory Affairs, and other stakeholders to ensure seamless coordination and successful trial execution
  • Help lead and monitor trial execution to ensure compliance with ICH/GCP guidelines, applicable regulations, and company policies
  • Organize and lead internal clinical project meetings, fostering collaboration and keeping teams aligned on goals and progress

In your first six months some projects you'll work on include:

  • Driving completion of critical milestones for the start of PRESERVE II clinical trial
  • Supporting the active PRESERVE I study long term follow up
  • Collaborating internally with other functions for clinical study implementation
  • Conducting clinical project team meetings

This position has a salary range of $145,000 - $165,000 annually. Ossium Health takes a market-based approach to pay. The successful candidate's starting salary will be determined based on, but not limited to, job-related skills, experience, qualifications, and market conditions. This range may be modified in the future.

We offer a full slate of employee benefits including:

  • Stock options
  • 401(k) matching
  • Medical, dental and vision coverage
  • Generous paid time off + 11 company holidays
  • Employer paid life insurance and long-term disability
  • Gym membership/recreational sports reimbursements