Clinical Trial Manager/Senior Clinical Trial Manager

Janux Therapeutics, Inc.; California; Hybride; USD 140 000 - 178 000; Plein temps

Avantages offerts par ce poste

Annual bonus program

Incentive stock option plan

401k plan

Comprehensive medical insurance

Dental and vision insurance

HSA/FSA

Unlimited PTO

Relocation assistance

Résumé du poste

Janux Therapeutics is seeking a Senior/Clinical Trial Manager to lead operational delivery for autoimmune programs in a fast-paced biotech setting. You will manage CROs, sites, and vendors, ensuring study deliverables meet ICH/GCP and SOP standards while maintaining timelines and budget.

You will partner with internal stakeholders and contribute to trial strategy, TMF completeness, and regulatory submissions, with limited travel and a hybrid work location in San Diego.

Qualifications

• Bachelor’s degree in life sciences with 5+ years CTM or 8+ years Sr. CTM experience.
• Experience in complex autoimmune trials including setup, monitoring and close-out.
• Knowledge of ICH/GCP regulations and regulatory expectations.
• Proficiency with eTMF, CTMS, EDC and related systems.

Responsabilités

• Oversee end-to-end clinical trial operations from start-up to close-out.
• Manage CROs, vendors, and sites to ensure on-time, on-budget delivery.
• Coordinate trial documentation, TMF readiness, and audits/inspections.
• Support study setup, regulatory submissions, and CSR readiness.
• Monitor metrics, drive issue resolution, and participate in process improvements.

Connaissances

CTM experience

GCP/ICH knowledge

Cross-functional collaboration

Communication skills

MS Office

Problem solving

Travel readiness

Formation

Bachelor’s degree in life sciences

Outils

eTMF

CTMS

EDC

Description du poste

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.

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 elevate 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.

Required Education, Experience, Skills, And Abilities

• Bachelor’s degree with at least 5 years (CTM) or 8 years (Sr. CTM) of hands-on clinical trial experience, preferably within a pharmaceutical or biotech environment. A combination of CRO and sponsor-side experience will be considered.
• Demonstrated experience in complex autoimmune clinical trials, including trial set-up, monitoring, and close-out.
• Strong working knowledge of ICH/GCP regulations.
• Proficiency with electronic systems such as eTMF, CTMS, EDC, etc.
• Ability to work independently with minimal oversight 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%).

$140,000 - $178,000 a year

In addition to a competitive base salary ranging from $140,000 to $154,000 for Clinical Trial Manager and $160,000 to $178,000, we offer stock options, restricted stock units, 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 hourly rate 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 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 and identifying potential inconsistencies or verification signals in application materials based on available information. 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.