

New · posted Oct 31
Janux Therapeutics · Biotechnology
Clinical Trial Manager/Senior Clinical Trial Manager (AID)
- San Diego, CA
- Hybrid
- Full-time
- Manager
The role
The Senior/Clinical Trial Manager will be responsible for managing and executing operational aspects of assigned clinical trials, from study start-up to close-out, with a focus on autoimmune studies. 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.
What you need
REQUIRED EDUCATION, EXPERIENCE, SKILLS, AND ABILITIES
Job Type: Full-time
What you'll do
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
- Support the successful execution of clinical trials from protocol concept to clinical study report in support of complex autoimmune programs.
- Prepare and maintain study-related files and documentation to ensure inspection readiness.
- 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 preparation for audits and inspections.
- Assist with budget management and day-to-day clinical operations in compliance with SOPs, ICH/GCP, and regulatory requirements.
- Track subject and site activity/metrics and perform quality checks across study components.
- Proactively identify and escalate issues related to functional 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.
- Coordinate with regulatory affairs on essential document submissions.
- Support study close-out activities including TMF and drug reconciliation and CSR readiness.
- Communicate effectively with study team members and work closely with Clinical Trial Managers and/or Asset Leads.
- Participate in process improvement and quality initiatives related to study execution.
- Other duties as deemed necessary.
Pay and benefits
$140,000 – $178,000 a year
Employer provided- Annual targeted bonus %
Annual bonus program
Incentive stock option plan
401k plan with flat non-elective employer contribution
100%
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
Where you'll work
San Diego, CAHybridOpen in Maps (opens in a new tab)
More jobs in San Diego, CASchedule and working conditions
Days
- Monday to Friday
Work authorization
- United States (Required)

From the posting
About Janux
Work Location
- Hybrid preferred in San Diego office. Remote permitted upon approval, with ability to travel 25% for meetings or site visits as required.
Equal opportunity, accessibility and legal noticesJanux Therapeutics's statements, word for word
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.
Job intelligence
The context around this role
Live data · October 31, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% below the US median for Clinical Trial Management roles at this level.
This roleEmployer provided
Manager roles in California10 roles publishing pay
Manager roles in the US26 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $140,000 | — | $178,000 |
| California (middle half) | $157,875 | $164,000 | $182,125 |
| All US (middle half) | $150,000 | $162,000 | $175,000 |
This role: Janux Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Trial Management roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Trial Management
The general path across 33 open Clinical Trial Management roles on Regulatory Jobs, with the titles they carry most. Not Janux's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 19 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs9
- Clinical trial conduct9
- Collaboration and leadership7
- GMP and compliance6
- Regulatory submissions2
- Lab testing and methods1
- Quality systems and risk1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Janux on Regulatory Jobs
- 5
- Open roles
- 5
- Distinct roles
- 1
- Locations
By discipline
- Clinical4 80%
- Regulatory1 20%
By level
- VP & Executive2 40%
- Director1 20%
- Manager1 20%
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Clinical Trial Manager/Senior Clinical Trial Manager (AID) at Janux
Open until filled. $140K–$178K a year, employer provided.

