Job Description
The Director of Pharmacovigilance will lead all safety-related activities across Janux's clinical development programs. This individual will ensure the safety of patients participating in clinical trials and the integrity of Janux's safety data. This role combines strategic leadership with hands-on execution, ensuring compliance with global regulatory requirements and the proactive integration of safety into drug development. The Director will also serve as a key liaison with regulatory authorities and internal stakeholders, driving a culture of safety and continuous improvement.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES: - Develop and execute pharmacovigilance strategies in alignment with Janux's clinical and regulatory goals.
- Represent Janux in safety-related interactions with global health authorities (e.g., FDA, EMA, APAC).
- Lead the development and implementation of safety management plans, risk management plans (RMPs), and signal detection strategies.
- Ensure safety is proactively integrated into clinical development and decision-making processes.
- Oversee the collection, evaluation, and reporting of adverse events (AEs) and serious adverse events (SAEs) from clinical trials.
- Manage external PV vendors and ensure timely, high-quality execution of contracted activities.
- Maintain a central repository and program plan for all PV activities and deliverables.
- Ensure readiness and execution of safety procedures in response to emerging safety concerns.
- Author and review PV-related documents including DSURs, SMPs, RMPs, RSIs, and safety sections of clinical protocols and study reports.
- Ensure compliance with global PV regulations (FDA, EMA, APAC, ICH, GVP) and internal SOPs.
- Monitor and ensure adherence to PV agreements and safety data exchange agreements (SDEAs) with partners.
- Support internal audits and regulatory inspections; conduct root cause analyses and implement CAPAs as needed.
- Serve as the safety representative in cross-functional teams, including clinical, regulatory, and medical affairs.
- Educate internal teams on evolving safety regulations and best practices.
- Lead or contribute to internal safety review meetings, DSMBs, and safety advisory committees.
- Other duties as deemed necessary
EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES - Graduate-level degree in life sciences, RN, or equivalent health-related training; MD or PharmD preferred.
- 8+ years of pharmacovigilance experience in the biotech or pharmaceutical industry, including proven leadership roles.
- Strong knowledge of global PV regulations (FDA, EMA, APAC, ICH, GVP).
- Experience in signal management, safety data interpretation, and regulatory reporting.
- Oncology and autoimmune experience will be prioritized in this role.
- MPH or pharmacoepidemiology training desirable.
- Demonstrated ability to lead cross-functional safety initiatives and influence decision-making.
- Excellent communication, analytical, and organizational skills.
- Proficiency in safety databases (e.g., Argus, ARISg) and MedDRA coding.
- Ability to travel domestically and internationally as needed.
$230,000 - $323,000 a year
In addition to a competitive base salary ranging from $230,000 to $323,000, 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, 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: • 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 theinterests 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.
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.
Job Tags
Full time, Summer work, Relocation package, Monday to Friday,