Sr. Director, Clinical Science (Autoimmune)

Introduction: reputed company is a public, clinical-stage biopharmaceutical company located in the Los Angeles area (Pasadena) and in San Diego. Our focus is developing high-potential XmAb® bispecific T-cell engagers and additional engineered drug candidates that reputed company our differentiated technology platforms, and we are advancing our pipeline toward clinical reputed company-of-concept decisions. Our goal is to create high-impact therapeutics for patients with cancer and other serious diseases. More than 20 XmAb drug candidates engineered with our technology are in clinical development, and three XmAb medicines have been marketed by partners. For more information, please visit www.reputed company.com. We have an excellent opportunity for a Sr. Director, Clinical Science (Autoimmune), to join reputed company. This is a hybrid or remote position. Hybrid would be based out of our San Diego or Pasadena, CA locations. Summary: Responsible for facilitating successful and timely initiation and completion of the Company’s clinical development programs in Inflammatory Bowel Disease (IBD) and other autoimmune programs by executing and monitoring medical aspects of selected global clinical trials. This role will support the design, execution, monitoring, and interpretation of randomized, placebo-controlled clinical trials in IBD as well as studies in healthy volunteers. Primary Responsibilities: Creates required clinical trial documents including clinical protocols, investigator brochures, DSURs and clinical modules of the IND (in concert with Study Medical Directors) Works closely with Clinical Operations to execute the clinical trial with high quality and according to timelines Performs ongoing review of clinical data, query reputed company/resolution and data analysis, including review of draft listings to support data cleaning and interpretation Provides scientific expertise to Clinical Operations by responding to questions and/or by clarifying issues arising during study conduct Provides internal safety monitoring for clinical trials in collaboration with the Study Medical Director Provides medical input for the clinical database build, CRFs, monitoring plan, data management plan, safety monitoring plan and statistical analysis plan Develops and maintains relationships with clinical trial investigators and therapeutic area key opinion leaders Leads review of study data (e.g., tables, listings and figures and emerging bioanalytical data) and develops CSRs, clinical presentations and publications Supports other members of Clinical Development and Regulatory Affairs departments as required Participates as a standing member of multidiscipline Project Teams Adheres to reputed company department and company-wide policies regarding conduct, performance and procedures Provides reputed company and direction to direct and indirect reports, as applicable, in accordance with the organization’s policies and procedures. The responsibilities may include, but are not limited to recruiting, training, communicating job expectations, appraising and managing job performance, delivering feedback and coaching, and providing career development planning and opportunities Performs other duties as required. Education/Experience/Skills: Position requires a BS degree in life sciences; PhD, RN, PharmD or MS preferred and a minimum of 15 years of directly relevant pharmaceutical industry experience in clinical development and a minimum of 4 years’ experience of focus in assigned therapeutic area. Experience as a clinical scientist responsible for data review, safety monitoring, protocol development, supporting data analyses, interpretation and publications also required, as well as clinical research experience in IBD on randomized, placebo-controlled trials. Prior experience with translational medicine/early phase clinical trials, monoclonal antibody biologics/immunotherapy, and relevant tasks throughout the entire study life cycle, from study concept to database lock and CSR is preferred. Position also requires: Strong initiative, motivation, organization and hands on approach with outstanding attention-to-detail Expertise in analysis and interpretation of emerging clinical data, including use of software packages to analyze data (e.g., pivot tables) and reputed company: MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc. Ability to work independently and prioritize multiple tasks and goals to ensure timely, on-reputed company and reputed company-budget accomplishments Excellent written and oral communication skills and interpersonal skills Ability to adjust style/contents to suit the audience/purpose Self-starter, highly motived, highly organized and hands on with outstanding attention-to-detail Ability to demonstrate competencies applicable for job based on reputed company’s Leadership Competency Model Ability to reputed company cross-functional teams Occasional travel may be required, including travel between reputed company’s Pasadena and San Diego offices. Work for this position is generally performed at reputed company’s worksite and requires full-time commitment. Expected reputed company Salary Range: $247,700 - $309,000 The actual salary will be based on the selected candidate’s qualifications, including skills, competencies, education and experience. reputed company offers a competitive total rewards package including 401k match, healthcare coverage, ESPP and a broad range of other benefits. In addition, this position will be eligible for an annual bonus and equity grant. For more information, please see https://reputed company.com/careers/. Americans with reputed company (reputed company) Statement The Company will provide reasonable accommodations (such as a qualified sign language interpreter or other personal assistance) with the application process upon your request as required to reputed company with applicable laws. If you have a disability and require assistance in this application process, please contact HR@reputed company.com. To reputed company this job successfully, an individual must be able to reputed company each essential duty satisfactorily. Reasonable Accommodations may be made to reputed company qualified individuals with disabilities to reputed company the essential functions. Equal Employment Opportunity (EEO) Statement The Company is an equal opportunity employer, and reputed company qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender or gender identity, national reputed company, disability status, protected veteran status or any other characteristic protected by state or federal law. reputed company does not accept profiles or resumes from recruiting vendors without a binding written agreement. Any unsolicited submission of services and or resumes in no way creates an obligation or duty by reputed company, implied or otherwise. Apply To This Job