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Director, Clinical Science

An integral member of the Janux Therapeutics’ Clinical Development team; the Director, Clinical Science will participate in the evaluation, strategic planning, design and execution of the drug development strategies of our current and future clinical-stage programs. The incumbent will work closely with the Clinical Operations team members to support and execute upon clinical trial conduct. In addition, they will support the assigned Clinical Lead with various deliverables necessary for successful clinical trial execution. 


ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:
  • Support the design and implementation of development strategies for programs entering the clinic, providing strategic clinical science input for all assigned programs
  • Collaborate cross functionally with Clinical Operations team members to support the design and execution of clinical trials. This may include assistance in the development of essential clinical trial documents such as protocols, ICF documents/amendments, CRF’s, CSR’s, and Investigator Brochures
  • Aid in the development of the Data Review Plan and Data Review Strategy, ensuring that protocol-level deviations, eligibility criteria, study assessments & other aspects of the protocol are implemented consistently across the study
  • Perform clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, working cross-functionally to monitor clinical data
  • Promote quality review of data with an emphasis on subject safety and eligibility, data integrity, trend identification, analysis and remediation, and identification of AEs/SAEs for medical review
  • Support ad-hoc Regulatory activities such as contributing by authoring/reviewing clinical portions of Regulatory Documents and/or posters, abstracts and manuscripts, and the preparation and conduct of meetings with regulatory agencies and/or external drug development consortiums
  • Develop and deliver upon clinical presentation slides and other materials for internal and external meetings
  • Maintain scientific and clinical knowledge in the specific therapeutic and disease areas of assignment
  • Other duties as required


EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES
  • Advanced degree in Life Sciences preferred
  • Minimum 8 years of industry experience, 5+ years of which dedicated to the conduct of clinical trials as a Clinical Scientist
  • Knowledge of Oncology drug development and clinical trial processes, study design, statistics and clinical operations within a similar biotech and/or pharmaceutical environment
  • Skills to support program-specific data review and trend analysis
  • Knowledge of the establishment and operation 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


$205,000 - $240,000 a year

In addition to a competitive base salary ranging from $205,000 to $240,000, 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.

 

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:

·         401K

·         Medical insurance

·         Dental insurance

·         Vision insurance

·         Supplemental disability insurance plans

·         Flexible schedule

·         Life insurance

·         Flexible vacation

·         Sick time

·         Incentive stock option plan

·         Relocation assistance

 

Schedule:

·         Monday to Friday

 

Work authorization:

·         United States (Required)

 

Additional Compensation:

·         Annual targeted bonus X%

 

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.

Average salary estimate

$222500 / YEARLY (est.)
min
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$205000K
$240000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Director, Clinical Science, Janux Therapeutics

Janux Therapeutics is on the lookout for a dynamic Director of Clinical Science to join our dedicated Clinical Development team in sunny San Diego, CA. This is a remarkable opportunity to play a key role in the strategic planning, design, and execution of our clinical-stage programs. As the Director, Clinical Science, you'll work closely with Clinical Operations to ensure our clinical trials run smoothly and successfully. Your experience will shine as you contribute to the creation of vital clinical trial documents including protocols and investigational brochures. You'll perform clinical data reviews and provide insights to ensure participant safety and data integrity. Plus, your leadership will help guide our regulatory activities, from preparing presentations for external meetings to engaging with regulatory agencies. With a strong background in Oncology drug development and clinical trial processes, you’ll be instrumental in shaping the future of our innovative therapies. If you’re ready to take your career to the next level with a company that values quality and collaboration, Janux Therapeutics is the place for you!

Frequently Asked Questions (FAQs) for Director, Clinical Science Role at Janux Therapeutics
What are the essential responsibilities for the Director, Clinical Science at Janux Therapeutics?

The Director, Clinical Science at Janux Therapeutics is responsible for designing and implementing drug development strategies for clinical programs. This role involves collaboration with the Clinical Operations team to support trial execution, developing essential clinical documents, performing data reviews, promoting quality assurance in trial data, and assisting with regulatory submissions. This leadership position ensures that all aspects of clinical trials align with company objectives and regulatory standards.

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What qualifications are needed for the Director, Clinical Science position at Janux Therapeutics?

Candidates for the Director, Clinical Science role at Janux Therapeutics should hold an advanced degree in Life Sciences and have a minimum of 8 years of industry experience, with at least 5 years focused on conducting clinical trials. Expertise in Oncology drug development, clinical operations, and data review processes is essential, along with strong project management and cross-functional team collaboration skills.

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How does the Director, Clinical Science contribute to clinical trial design at Janux Therapeutics?

The Director, Clinical Science plays a crucial role in clinical trial design at Janux Therapeutics by providing strategic input for the development of clinical programs. This includes the preparation of comprehensive clinical trial documents and collaborating with the Clinical Operations team to ensure that the trial design is robust, compliant, and aligned with regulatory standards. Their expertise helps shape the framework within which clinical research is conducted to achieve successful outcomes.

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What type of experience is needed to excel as a Director, Clinical Science at Janux Therapeutics?

To excel as a Director, Clinical Science at Janux Therapeutics, candidates should have in-depth knowledge of Oncology drug development and a strong foundation in clinical trial processes. Experience in analyzing clinical data, identifying trends, and ensuring compliance with Good Clinical Practice (GCP) is critical. Effective communication skills and the ability to lead cross-functional teams are also vital for success in this role.

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What are the workplace benefits for the Director, Clinical Science at Janux Therapeutics?

Janux Therapeutics offers a competitive salary for the Director, Clinical Science position, ranging from $205,000 to $240,000, along with stock options and a comprehensive benefits package. Employees can enjoy medical, dental, and vision insurance, a flexible schedule, generous vacation policies, and a 401K plan. Additionally, Janux is committed to fostering an inclusive work environment and provides support for relocation.

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Common Interview Questions for Director, Clinical Science
Can you describe your experience with clinical trial design in your role as a Clinical Scientist?

In your response, focus on specific instances where you contributed to the design of clinical trials, detailing your strategic input and collaboration with other teams. Highlight how your expertise has shaped trial designs to meet regulatory requirements and improve patient outcomes.

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How do you approach data review and analysis in your role as a Director of Clinical Science?

Discuss your systematic approach to reviewing clinical data, the tools you use for analysis, and how you ensure data integrity and subject safety. Providing examples of past analyses and the impact of your findings on decision-making will demonstrate your skills effectively.

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What strategies do you implement to collaborate effectively with cross-functional teams?

Describe specific strategies or tools you utilize for effective collaboration, such as regular meetings, project management software, or shared documentation. Mention how these strategies contribute to successful clinical trial outcomes and teamwork.

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Can you discuss your experience with regulatory submissions and interactions?

Share your experiences with preparing regulatory documents and meetings, emphasizing your understanding of regulatory requirements. Highlight successful interactions with regulatory agencies and how your contributions supported critical submissions.

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What metrics do you consider important in evaluating clinical trial success?

Explain the key performance indicators (KPIs) you focus on when evaluating trial success. This can include patient recruitment rates, data integrity measures, and adherence to timelines. Make sure to back your claims with relevant examples.

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How do you ensure the safety and well-being of participants in your clinical trials?

Discuss the protocols and practices you follow to monitor patient safety and eligibility criteria. Highlight your dedication to ethical standards in research and any specific processes you have implemented to enhance participant safety.

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What experience do you have in training and mentoring clinical trial staff?

Share your approaches to mentoring staff, the importance of training in adhering to protocols, and how this has positively influenced team performance. Examples of training sessions or materials you’ve developed could strengthen your response.

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Can you provide an example of a clinical trial challenge you faced and how you resolved it?

Present a challenging situation that you navigated in a clinical trial, detailing the steps you took to resolve it and the outcome. This will showcase your problem-solving skills and your ability to remain composed under pressure.

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What advancements in oncology research are you most excited about?

Express your enthusiasm for current trends in oncology research, linking them to your experience. Discuss how these advancements might impact future clinical trials and how you hope to contribute to them.

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How do you stay updated with the latest regulations and guidelines affecting clinical trials?

Detail your strategies for keeping abreast of industry regulations and guidelines, such as attending conferences, reading scientific journals, and participating in professional networks. This shows that you are proactive and committed to your professional development.

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EMPLOYMENT TYPE
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DATE POSTED
April 6, 2025

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