Job Description Responsibilities Evaluate pre‑clinical and translational work to generate early clinical development plans and Investigational New Drug (IND) applications. Provide clinical development support for business development assessments of external opportunities to grow the Immunology pipeline. Develop clinical development strategies for investigational drugs and design, plan, and conduct clinical trials (including operational plans and study settings). Monitor and manage ongoing or new clinical trials for investigational drugs. Analyze and summarize clinical findings (safety, efficacy) to support decisions on new drug applications, clinical study reports, and publications. Participate in internal and joint internal/external research project teams relevant to the development of new compounds. Supervise Clinical Scientists in the execution of clinical studies. Collaborate with cross‑functional experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects and inform senior leadership of study progress. Maintain a strong scientific knowledge base by staying current on scientific developments, research methodologies, and new findings in Immunology. Identify and establish collaborative relationships with external experts in Rheumatology, Gastroenterology, Dermatology, Pulmonary, or rare diseases to inform development of investigational drugs. Attend scientific meetings to maintain competency and awareness of research activities. Author detailed development documents, presentations, budgets, and position papers for internal and external audiences. Facilitate collaborations with external researchers globally. Travel on company business approximately 20% of the time to manage future or ongoing clinical research projects. Qualifications Minimum education: M.D., D.O., M.D./Ph.D., or D.O./Ph.D. Experience designing and/or executing Phase 2 or Phase 3 clinical trials in Immunology. Minimum 3 years of clinical medicine experience. Minimum 5 years of industry experience in drug development. Demonstrated record of scientific scholarship and achievement. Strong interpersonal skills and ability to work collaboratively in a cross‑functional team environment. Proficiency in Clinical Development, Clinical Documentation, Clinical Immunology, Clinical Judgment, Clinical Medicine, Clinical Research Management, Clinical Sciences, Clinical Studies, Clinical Trial Development, Data Analysis, Drug Development, Scientific Consulting, and Strategic Planning. Benefits Medical, dental, vision, and other healthcare insurance benefits for employee and family. Retirement benefits including 401(k). Paid holidays, vacation, compassionate leave, and sick days. Eligible for annual bonus and long‑term incentive, if applicable. Comprehensive benefits package available through the company portal. Salary Salary range: $282,200.00 – $444,200.00. The actual salary will be based on education, qualifications, experience, skills, location, and business needs. EEO Statement As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under U.S. Equal Opportunity Employment laws, visit the EEOC or consult respective MeCM website. Location Requirements SanFrancisco Residents Only: Candidates must meet the SanFrancisco Fair Chance Ordinance requirements. LosAngeles Residents Only: Candidates will be considered in accordance with the City of LosAngeles Fair Chance Initiative for Hiring Ordinance. #J-18808-Ljbffr