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Jobs at Janux Therapeutics (Now Hiring) — 3 open

Janux Therapeutics logoJanux Therapeutics

Associate Director, Clinical Operations

San Diego, California, United States · On-site

$175k–$200k/yr

Senior$899M raised

The Associate Director, Clinical Operations will be responsible for managing operational aspects of assigned clinical trials, with a focus on early-phase oncology studies. This includes oversight of contract research org…

Skills: Clinical operations, Oncology, Clinical trials, GCP, FDA regulations

Janux Therapeutics logoJanux Therapeutics

Vice President, Biometrics

San Diego, California, United States · Hybrid

$330k–$360k/yr

Senior+$899M raised

The Vice President, Biometrics will lead and oversee all biometrics activities supporting clinical development from IND-enabling studies through regulatory submission. This role is responsible for Biostatistics, Statisti…

Skills: Biostatistics, Statistical Programming, Clinical Data Management, Clinical Trial Design, Regulatory Submission

Janux Therapeutics logoJanux Therapeutics

Senior Director, Clinical Operations

San Diego, California, United States · Hybrid

$245k–$260k/yr

Senior+$899M raised

The Senior Director of Clinical Operations will provide global operational leadership overseeing complex clinical programs focusing on innovative T-cell engager therapies for immunology and oncology indications. This rol…

Skills: Clinical Operations Strategy, Clinical Trial Management, ICH-GCP, FDA Regulations, CRO Management

Janux Therapeutics logo

Associate Director, Clinical Operations

Janux Therapeutics

San Diego, California, United States • On-site

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  • $175k–$200k/yr
  • Full-time
  • Annual bonus program, Incentive stock option plan, 401k plan, Medical insurance, Dental insurance, Vision insurance
  • Posted 1d ago
  • ~40 hrs/week

Responsibilities

The Associate Director will manage the operational execution of early-phase oncology clinical trials, including oversight of CROs, vendors, and clinical sites. They are responsible for ensuring trial compliance with GCP and regulatory standards while leading cross-functional teams to meet quality and budget targets.

Requirements

The role requires deep expertise in managing early-phase oncology trials within a sponsor biotech environment. Candidates must possess a strong understanding of clinical trial processes, regulatory compliance, and the ability to mentor team members while managing complex study documentation.

Full job description

The Associate Director, Clinical Operations will be responsible for managing operational aspects of assigned clinical trials, with a focus on early-phase oncology studies. This includes oversight of contract research organizations (CROs), vendors, and clinical sites across both U.S. and international regions. The role requires a deep understanding of clinical trial processes, regulatory compliance (GCP, FDA, ICH), and the ability to lead cross-functional teams to ensure high-quality, timely, and cost-effective trial execution. The ideal candidate will bring an in-depth understanding of managing early phase oncology trials at a sponsor biotech.

\nESSENTIAL FUNCTIONS AND RESPONSIBILITIES
  • Lead the planning, initiation, execution, and close-out of complex Phase I oncology trials. Ensure all trial activities are conducted in accordance with the protocol, SOPs, GCP, and applicable regulations.
  • Manage and oversee external partners including CROs, central labs, biometrics, safety vendors, eTMF providers, and others. Ensure deliverables are met on time, within budget, and to quality standards.
  • Manage, mentor, and support direct reports, fostering professional development and team performance.
  • Participate in site selection, feasibility assessments, and initiation visits. Build strong relationships with investigators and site staff to support efficient enrollment and high-quality data collection.
  • Oversee the development and review of essential study documents such as protocols, informed consent forms, case report forms (CRFs), monitoring plans, and study manuals.
  • Review monitoring reports and ensure timely resolution of issues. Provide guidance to CRO monitors and ensure appropriate sponsor oversight is documented.
  • Conduct ongoing data reviews and support data cleaning activities. Ensure inspection readiness at all times, including regular review of the Trial Master File (TMF).
  • Collaborate with finance and legal teams to manage study budgets, review vendor invoices, and negotiate contracts and change orders.
  • Work closely with internal stakeholders including Clinical Development, Data Management, Regulatory Affairs, Medical Affairs, and CMC to ensure alignment and smooth execution of clinical programs.
  • Provide guidance and mentorship to junior team members and cross-functional colleagues. Share best practices and contribute to continuous process improvement.
  • Prepare and deliver study updates, metrics, and presentations to senior leadership. Represent Clinical Operations in internal and external meetings.
  • Contribute to the development and implementation of SOPs, work instructions, and operational tools to enhance team efficiency and compliance.
  • Willingness to travel up to 15% for site visits, vendor meetings, and conferences.
  • Other activities as assigned.
\n
$175,000 - $200,000 a year

In addition to a competitive base salary ranging from $175,000 to $200,000, 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 base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, internal equity, and work location.

\n

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:

·         On site (San Diego, CA)

 

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.

Notice to Recruiters and Third-Party Agencies

The Talent Acquisition team manages the recruitment and employment process for Janux. To protect the interests of all parties involved, Janux will only accept resumes from a recruiter once a fully-executed search agreement is in place. Agencies are hereby specifically directed not to contact Janux employees directly in an attempt to present candidates. Janux will consider any candidate for whom an Agency and/or Recruiter has submitted an unsolicited resume to have been referred, free of any charges or fees.

Related keywords

Clinical OperationsOncologyPhase I TrialsCROGCPFDAICHSOPeTMFBiometricsSite SelectionFeasibilityInformed ConsentCRFMonitoring PlansData Cleaning

About Janux Therapeutics

LinkedInVisit site
Industry
Biotechnology Research
Company size
51-200 employees
Founded
2017
Headquarters
San Diego, California
LinkedIn followers
13,400
Total funding
$899M

Janux is a clinical-stage company developing unique immunotherapies that have the potential to generate tumor-specific immune responses to attack and kill tumors without destroying a patient’s healthy tissue. Janux is using its platform masking technology to engineer novel drug candidates that are designed to overcome the traditional T cell engager toxicity and efficacy limitations. Janux is proud to have earned a 𝐆𝐫𝐞𝐚𝐭 𝐏𝐥𝐚𝐜𝐞 𝐓𝐨 𝐖𝐨𝐫𝐤 𝐂𝐞𝐫𝐭𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧™ in 2024.

Offices: 10955 Vista Sorrento Pkwy, Suite 200, San Diego, California 92130, US

BiotechnologyHealth DiagnosticsBiotechnologyPharmaceuticalTherapeutics
View all jobs at Janux Therapeutics

About Janux Therapeutics

LinkedInVisit site
Industry
Biotechnology Research
Company size
51-200 employees
Founded
2017
Headquarters
San Diego, California
LinkedIn followers
13,400
Total funding
$899M

Janux is a clinical-stage company developing unique immunotherapies that have the potential to generate tumor-specific immune responses to attack and kill tumors without destroying a patient’s healthy tissue. Janux is using its platform masking technology to engineer novel drug candidates that are designed to overcome the traditional T cell engager toxicity and efficacy limitations. Janux is proud to have earned a 𝐆𝐫𝐞𝐚𝐭 𝐏𝐥𝐚𝐜𝐞 𝐓𝐨 𝐖𝐨𝐫𝐤 𝐂𝐞𝐫𝐭𝐢𝐟𝐢𝐜𝐚𝐭𝐢𝐨𝐧™ in 2024.

Offices: 10955 Vista Sorrento Pkwy, Suite 200, San Diego, California 92130, US

BiotechnologyHealth DiagnosticsBiotechnologyPharmaceuticalTherapeutics
View all jobs at Janux Therapeutics

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