Director, Clinical Science

Janux Therapeutics

Director guiding clinical science for Janux Therapeutics’ early-stage oncology immunotherapy programs. Supporting trial strategy, data review, regulatory materials, and clinical milestones.

Posted 8/6/2026full-timeSan Diego • California • 🇺🇸 United StatesLead💰 $236,000 - $255,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical trial design and execution, with a strong focus on oncology drug development and regulatory compliance. Proficient in data review and trend analysis, ensuring data integrity and subject safety throughout the clinical process.

Highest-signal resume keywords

Clinical Trial DesignOncology Drug DevelopmentData Review and Trend AnalysisRegulatory ComplianceProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Protocol DevelopmentICF Document PreparationCRF DevelopmentCSR WritingInvestigator Brochure CreationStatistical AnalysisGCP KnowledgeData Monitoring Committee KnowledgeDose Review Team KnowledgeIndependent Response Adjudication Knowledge

Soft Skills

Critical EvaluationCross-Functional Team LeadershipCollaborationCommunication

Industry Keywords

Clinical OperationsBiotechPharmaceuticalRegulatory DocumentsPatient SafetyEligibility CriteriaData IntegrityAdverse Event IdentificationClinical Science InputTherapeutic Areas

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support the design and implementation of development strategies for programs entering the clinic, providing strategic clinical science input
Collaborate with Clinical Operations on the design and execution of clinical trials
Assist in developing clinical trial documents, including protocols, ICF documents/amendments, CRFs, CSRs, and Investigator Brochures
Aid in developing the Data Review Plan and Data Review Strategy
Perform clinical data review and identify insights through patient-level review and trend analysis
Promote quality review of data with emphasis on subject safety, eligibility, data integrity, trends, remediation, and AE/SAE identification
Support regulatory activities by authoring or reviewing clinical portions of regulatory documents, posters, abstracts, and manuscripts
Prepare for and conduct meetings with regulatory agencies and external drug development consortiums
Develop and deliver clinical presentation slides and materials for internal and external meetings
Maintain scientific and clinical knowledge in assigned therapeutic and disease areas
Perform other duties as required

Requirements

What you’ll need

BS in life sciences or related field
Minimum 8 years of industry experience, including 5+ years conducting clinical trials as a Clinical Scientist
Knowledge of oncology drug development and clinical trial processes
Knowledge of study design, statistics, and clinical operations in a similar biotech or pharmaceutical environment
Skills supporting program-specific data review and trend analysis
Knowledge of data monitoring committees, dose review teams, and independent response adjudication committees
Knowledge of GCP and regulatory requirements
Ability to critically evaluate data, literature, and presentations
Ability to lead and work with cross-functional teams
Strong project management skills
United States work authorization required

Benefits

Comp & perks

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, including summer and winter company shutdown
Relocation assistance
Stock options
Restricted stock units
Stock purchase plan (ESPP)
Target bonus
Comprehensive benefits package for employees and their families
Supplemental disability insurance