Position Description


We are seeking an entrepreneurial Medical Immunologist to assume the role of Senior Medical Director for our innovative allogeneic regulatory T cell therapy programs. The ideal candidate thrives in a dynamic, fast-paced startup environment and is eager to embrace new challenges. This pivotal position, reporting directly to the Chief Medical Officer, involves contributing to design and overseeing clinical trials from phase I to later phase 2 and 3 leading to BLA. As a key member of our organization, you will have significant exposure to executive leadership. This role is based at our San Diego headquarters.


Key Responsibilities



  • Spearhead and collaborate with cross-functional study teams, including clinical research scientists, clinical operations, regulatory affairs, and biostatistics, to ensure the successful execution of the trial.

  • Develop and execute the clinical development and business strategy for product development in autoimmune disease indications

  • Orchestrate the design, initiation, execution, analysis, and dissemination of clinical studies

  • Actively participate in study team meetings, investigator meetings, and other relevant forums to discuss trial progress, challenges, and opportunities

  • Cultivate relationships with external clinical researchers and KOLs

  • Provide medical expertise and guidance throughout the trial, including patient screening, enrollment, and management

  • Convene and facilitate advisory boards with industry experts and investigators

  • Author clinical study protocols and recommend trial sites, investigators, data outputs, and publications

  • Ensure compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and study protocols

  • Collaborate with Clinical Operations to optimize trial execution

  • Provide support for regulatory activities, medical affairs, and payer engagements

  • Represent the company at external scientific and medical forums

  • Manage annual budgets and operating plans for clinical studies

  • Undertake additional duties as required


The Team – Yes You Belong!


We are building a diverse, bold, agile, and collaborative organization where each team member works closely and communicates respectfully with each other. Tr1X leadership has high expectations for themselves and for you (and so should you!): we expect the company and all its employees to be deeply focused on bringing Tr1X's cellular therapies to patients at an accelerated pace. Key attributes include a can do attitude, a strong work ethic, a collaborative spirit, and excellent interpersonal and communication skills.


Qualifications:



  • Medical degree with specialization in Neurology (preferred), Immunology, Rheumatology, Nephrology or Gastroenterology

  • Minimum 5 years of pharmaceutical or biotech industry experience, demonstrating proficiency in all development phases

  • Extensive knowledge and experience in clinical research within an industry setting

  • Experience in cellular therapy development is highly advantageous

  • Comprehensive understanding of related disciplines (biostatistics, regulatory affairs, pharmacology, toxicology, cell therapy manufacturing, clinical pharmacology, and pharmaceutical sciences)

  • Proven ability to collaborate across departments (Clinical Operations, Translational Research, R&D, Regulatory Affairs, Finance, Manufacturing, Process and Analytical Development)

  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and external stakeholders

  • Ability to thrive in a fast-paced and dynamic environment with a proactive and adaptable approach to challenges

  • Self motivated, with the ability to motivate and inspire teams to achieve results

  • Meticulous attention to detail with strong multitasking abilities, analytical mindset, and problem-solving abilities

  • Demonstrated scientific output (publications, abstracts, etc.)

  • Strong knowledge of Good Clinical Practices, FDA regulations and guidelines and applicable regulatory requirements.

  • Ability to effectively evaluate outside expert advice.

  • Ability to communicate and explain immunologic and/or cell therapy technical issues to clinical, regulatory, biomarker, biostatistics, data management and manufacturing colleagues who may have a non-medical background.

  • Authorization to work in the United States


We offer:



  • Anticipated Base Salary Range: $250,000 - $350,000

  • In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, and 401k match

  • We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance

  • The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience and education


Location:


This is an in-person role based at our San Diego headquarters, with a minimum three day a week on site presence. Travel up to 15% of the time may be required.