Autobahn Therapeutics is a biotechnology company developing a portfolio of neuropsychiatric and neuroimmunologic clinical candidates leveraging its brain-targeting chemistry platform. Autobahn aims to unlock new therapeutic opportunities through precision tuning of CNS exposure, pursuing validated clinical and biologic targets, and guiding development with biomarkers. The company’s pipeline is led by ABX-002, a thyroid hormone receptor beta (TRβ) agonist being developed as a potential adjunctive treatment for people with major depressive disorder and bipolar disorder depression. Autobahn Therapeutics is based in San Diego.AboutAutobahn’s Clinical Development function is responsible for strategic planning, advancing and execution early through late-stage clinical development (Phase I/II/III) programs of our innovative and differentiated CNS therapeutic assets. We are seeking a dynamic and highly skilled professional to fill the role of Clinical Scientist. This role integrates key responsibilities from clinical science and clinical trial support functions. The successful candidate will bridge scientific expertise, clinical trial management, and stakeholder engagement to support the development, execution, and communication of clinical trial data. Reporting to the Head of Clinical Development, the ideal candidate will act as a strategic partner to both internal teams and external partners to ensure the smooth progress of clinical research, while translating scientific and clinical insights into meaningful discussions with key stakeholders.ResponsibilitiesEssential Functions/Responsibilities- Collaborates with internal teams (Clinical Operations, Regulatory, Medical Affairs) to provide scientific insights and expertise for the design and optimization of clinical trial protocols.- Supports clinical development team to implement clinical trial protocols that align with scientific goals and regulatory requirements.- Ensures the integrity and quality of clinical trial data and consistency with trial objectives.- Reviews clinical study data, querying discrepant data/information to ensure accurate data reporting.- In collaboration with biometrics, develops and QCs data tables, listings, and figures, and develops study-specific fit-for-purpose analyses.- Collaborates with the clinical development team on analysis and interpretation of study results and contributes to clinical study report content and interpretation of research results.- Collaborates with Corporate Development to articulate the clinical value story behind study results for external audiences (i.e. publications, posters, manuscripts etc.).- Assists with preparing responses to questions from health authorities and ethics committees; interactions with site IRBs/ethics committees and/or review committees as needed.- Assists with preparing clinical scientific presentations, including meeting abstracts, posters, oral presentations, and advisory boards.- Analyzes and interprets clinical trial progress and study data, providing actionable insights to drive decision-making.- Collaborate with clinical operations teams to ensure high-quality site management and successful recruitment, retention, and adherence to clinical protocols.- Supports the development of clinical communication materials and clinical trial documentation including study plans, informed consent forms, and site training materials.- Tracks site performance, identify risks, and provide solutions to enhance site engagement and study completion.RequirementsQualifications- Advanced degree (PhD, PharmD, or equivalent) in life sciences, medicine, pharmacology, or related fields.- Minimum of 6 years of experience in clinical research or clinical trials, ideally in a pharmaceutical or biotechnology environment.- Expertise in scientific data analysis, with the ability to derive actionable insights for clinical and medical decision-making.- Understanding of clinical trial design, Good Clinical Practice guidelines, regulatory requirements, and therapeutic area knowledge.- Proven ability to communicate complex scientific concepts clearly and effectively, both in writing and verbally.- Experience writing regulatory documents and protocols.- Experience using electronic data capture (EDC) tools.- Experience using data analytics software.- Excellent interpersonal, communication (oral and written), and analytical skills.- Highly organized with strong project management skills and attention to detail.- Exceptional relationship-building skills, capable of engaging with diverse stakeholders (investigators, internal teams, etc.).- Strong problem-solving abilities to address clinical trial challenges.- Ability to work independently and in a highly collaborative, team-oriented environment.Preferred Qualifications- Experience leading or contributing to neuropsychiatry/neurology clinical development programs highly desirable.- Prior experience in both early-phase and late-phase clinical trials.Compensation and BenefitsThe salary range for this position is $200,000 to $230,000 per year, which factors in various geographic regions. The actual compensation and seniority level for this position will be determined based on relevant experience and qualifications. In addition to a competitive base salary, this position is also eligible for discretionary bonus and equity awards based on factors such as individual and organizational performance. We offer a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, life, disability and a 401(k) plan with company matching.How to ApplyFor consideration, please apply via LinkedIn or email us with your resume referencing Associate Director, Clinical Science in the subject line to careers@autobahntx.com.EEOWe foster an environment where all people are afforded the freedom to pursue their passions without regard to race, color, religion, national or ethnic origin, gender (including pregnancy), sexual orientation or expression, age, disability or veteran status or any other characteristics protected by law.
