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Live In Remote Clinical Trial Manager Jobs (NOW HIRING)

Avery Healthcare Group Ltd.

Lead Clinical Trial Manager - remote Job Location: Connecticut, USA Job Location Type: Remote Job ... In this role, you will be pivotal in overseeing clinical studies from inception to completion ...

Icon plc

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

Senior Clinical Trial Manager, Biotech - Remote, US ICON is a global healthcare intelligence and ... A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or ...

Braveheart Bio

$140K - $170K/yr

Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our ... This position is for remote work and may require domestic or international travel up to 25% (as ...

Braveheart Bio

Clinical Trial Manager

Manhattan, NY · On-site +1

Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our ... for remote work and may require domestic or international travel up to 25% (as needed); valid ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

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 ...

ICON

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

Efficient communication with the Clinical Trial Managers (CTMs), Clinical Operations and the Global ... Degree in a health or science related field. * 3 - 5+ years of trial end to end management ...

Braveheart Bio

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our ... This position is for remote work and may require domestic or international travel up to 25% (as ...

AA Inclusion

Clinical Trial Manager/Project Manager (US-East-Coast Remote) The Clinical Trial Manager (CTM) is ... In addition, the Clinical Trial Manager (CTM) proactively identifies, resolves/mitigates and ...

ICON

Senior Clinical Trial Manager

Bachelor's degree in health, life sciences, or other relevant fields of study. * At least 10+ years of relevant experience in clinical trial management. * Preferred: 2+ years of monitoring experience.

Character Biosciences

Senior Clinical Trial Manager

$153K - $180K/yr

Founded in 2018, Character has raised capital from leading investors at the intersection of health ... Remote The Opportunity : Character Biosciences is seeking a Senior Clinical Trial Manager who will ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Lead the oversight of CROs and vendors in partnership with the rest of the Clinical Operations team ... Perform clinical research site activities, which can include onsite or remote monitoring, co ...

Worldwide Clinical Trials

Clinical Trial Manager

NC · On-site +1

Why Worldwide We believe everyone plays an important role in making a world of difference for ... Provide leadership and direction to clinical site management team members from study start through ...

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How much do live in remote clinical trial manager jobs pay per hour?

As of May 28, 2026, the average hourly pay for live in remote clinical trial manager 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.
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Clinical Trial Manager/Sr. CTM

Clinical Trial Manager/Sr. CTM

Janux Therapeutics

San Diego, CA • On-site, Remote

$134K - $153K/yr

Full-time

Posted 29 days ago

Job description

The Clinical Trial Manager/Sr. CTM will play a pivotal role in the strategic implementation and execution of clinical trials from study start-up to close-out. This individual will be instrumental in managing and overseeing CROs, study vendors, and clinical trial sites, while partnering with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in accordance with regulatory requirements, GCP guidelines, and internal SOPs. This position reports directly to the Senior Director of Clinical Operations and serves as an integral member of the Clinical Operations team, contributing to the development of trial strategy, executing initiatives, and ensuring the highest standards in operational delivery. This is a great opportunity to make a meaningful impact in a fast-paced, mission-driven biotech environment.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
  • Lead the successful execution of clinical trials from protocol concept to clinical study reports in support of complex oncology programs.
  • Ensure inspection readiness by maintaining comprehensive study documentation and files.
  • Organize and lead study and departmental meetings, including minute-taking and document archiving.
  • Coordinate clinical trial equipment, supplies, and cross-functional project activities (e.g., Clinical Data Review Meetings).
  • Ensure team compliance with study-specific training and perform TMF reviews for completeness.
  • Support clinical sites in audit and inspection preparation.
  • Assist with budget management and daily clinical operations, ensuring adherence to SOPs, ICH/GCP, and regulatory requirements.
  • Monitor subject and site activity/metrics and perform quality checks across study components.
  • Proactively identify, troubleshoot, and escalate issues impacting deliverables.
  • Contribute to study set-up activities including protocol/synopsis development, informed consent forms, system configuration (CTMS, IRT), regulatory submissions, and operational documentation.
  • Collaborate with CROs to ensure timely collection and archiving of TMF documents.
  • Partner with regulatory affairs on essential document submissions.
  • Support study close-out activities including TMF and drug reconciliation and CSR readiness.
  • Foster effective communication and collaboration with study team members, Clinical Trial Managers, and Asset Leads.
  • Participate in process improvement and quality initiatives related to study execution.
  • Other duties as deemed necessary.
REQUIRED EDUCATION, EXPERIENCE, SKILLS, AND ABILITIES
  • Bachelor’s degree with at least 5 years of hands-on clinical trial experience, within a pharmaceutical or biotech environment. A combination of CRO and sponsor-side experience will be considered.
  • Demonstrated experience in oncology trials, including trial set-up, monitoring, and close-out.
  • Global clinical trial management experience, especially in the EU, highly desirable.
  • Strong working knowledge of ICH/GCP regulations.
  • Proficiency with electronic systems such as eTMF, CTMS, EDC, etc.
  • Ability to work independently and thrive in a collaborative team environment.
  • Strong critical thinking skills, a sense of urgency, and a proactive problem-solving mindset.
  • Excellent interpersonal, written, and verbal communication skills.
  • Proficiency in MS Office and comfort with technology.
  • Minimal travel required (0 to 5%).
In addition to a competitive base salary ranging from $134,000 to $153,000 for a Clinical Trial Manager and $154,000 to $170,000 for a Senior Clinical Trial Manager, we offer stock options, a stock purchase plan (ESPP) and a target bonus.  Janux also provides a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance. Relocation assistance may also be available.
 
Please note that the salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, and internal equity.
Job Type: Full-time
Benefits:
·             Annual bonus program
·             Incentive stock option plan
·             401k plan with flat non-elective employer contribution
·             Comprehensive medical insurance with 90-100% employer-paid premiums
·             Dental and vision insurance
·             HSA, FSA, and supplemental insurance plans (life, disability, accident, critical illness, hospital indemnity)
·             Unlimited PTO
·             Generous holiday schedule; includes summer and winter company shutdown
·             Relocation assistance
Schedule:
·             Monday to Friday
Work authorization:
·             United States (Required)
Additional Compensation:
·             Annual targeted bonus %
Work Location:
·             Hybrid preferred in San Diego office. Remote permitted upon approval, with ability to travel up to 25% for meetings or site visits as required.
 
EQUAL OPPORTUNITY EMPLOYER:
Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.