Vera Therapeutics, Inc.
Associate Director, Clinical Scientist
Vera Therapeutics, Inc., Brisbane, California, United States, 94005
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Associate Director, Clinical Scientist
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Vera Therapeutics, Inc. Vera Therapeutics (Nasdaq: VERA) is a late clinical-stage biotechnology company focused on developing treatments for serious immunological diseases. Veras lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation Inducing Ligand (APRIL). Vera is also developing VT-109, a novel, next-generation dual BAFF/APRIL inhibitor in preclinical development, and MAU868, a monoclonal antibody designed to neutralize BK virus infection. For more information, please visit: www.veratx.com. Our values are the cornerstone of our culture. Our values guide everything we dofrom how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases. Position Summary
The Associate Director, Clinical Scientist will report to the Senior Director, Clinical Development and will be responsible for the development, evaluation, planning, and execution of clinical studies, ensuring scientific integrity and the interpretation of study data within a clinical development program. Working closely with cross-functional teams, contributing to drug-candidate development projects in both early and/or late-phase clinical development. The Associate Director, Clinical Scientist reports to Sr. Director, Clinical Development. Responsibilities
Support or assist the Clinical Development lead for a program and/or contribute as a key member of the Clinical Study Team. Actively participates in program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings, and may contribute to collaborative activities with other departments. Maintain a strong understanding of therapeutic disease areas and drug candidates, including underlying disease biology, clinical manifestations, therapeutic standard practices, compound mechanisms of action, and the competitive drug landscape. Assist with the design and execution of clinical research studies for early and/or late-stage assets, contributing to strategy development and proposals grounded in scientific literature. Author and/or review documents related to trials, such as medical monitoring plans, SAPs, informed consents, and clinical components of Clinical Study Reports. Support regulatory document development, quality reviews, and cross-functional comment resolution. Prepare information for stakeholder meetings (e.g., investigator meetings, governance, DMCs, regulatory authorities, scientific advisory boards, study steering committees) and may present data at external investigator meetings (SIV) and internal collaborations. Support clinical/medical data review, including safety monitoring activities and ensure patient safety in compliance with FDA, EMEA, ICH, and GCP guidelines, as well as applicable SOPs. Ensure consistent application of medical/clinical data review techniques across studies/programs and contribute to the drafting/updating/reviewing of medical/clinical data review plans for assigned studies. Qualifications
Bachelor's Degree in a related field and 5+ years of related scientific experience OR an advanced degree (Ph.D., Sc.D., M.S., M.P.H., PharmD) with 3+ years of related scientific experience. Experience in clinical research, with a focus on glomerular disease, autoimmune disease, or nephrology is a plus. Strong ability to critically analyze, interpret, and summarize data in a clear, scientifically accurate manner. Well-developed interpersonal and communication skills, with experience collaborating across teams and building strong, positive relationships. Strong organizational skills with the ability to manage multiple competing priorities in a fast-paced environment. High attention to detail and strong project management skills. Solid understanding of scientific writing principles, with the ability to communicate complex information clearly and concisely. Proficient in scientific writing tools (e.g., Microsoft Office suite, document management systems, reference management software) and ability to quickly learn new software applications. Vera Therapeutics Inc. is an equal-opportunity employer. Vera Therapeutics is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $ - $. The exact base pay offered will depend on factors including geography, qualifications, skills, and experience. At Vera, base pay is only one part of total compensation, which may include an annual performance incentive bonus, new hire equity, and ongoing performance-based equity, as well as benefits (medical, dental, vision, 401k match, flexible time off, and holidays). Notice to Recruiters/Staffing Agencies
Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors are prohibited from contacting our hiring managers, executives, or employees without a fully executed written agreement. Fraud Alert
Your personal information and online safety are a top priority. Please apply through our official career page at https://veratx.com/careers/. Recruiters will contact you using the veratx.com domain, and we will never request payments or sensitive information. If unsure, email human resources. Seniority level
Mid-Senior level Employment type
Full-time Job function
Health Care Provider
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Associate Director, Clinical Scientist
role at
Vera Therapeutics, Inc. Vera Therapeutics (Nasdaq: VERA) is a late clinical-stage biotechnology company focused on developing treatments for serious immunological diseases. Veras lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation Inducing Ligand (APRIL). Vera is also developing VT-109, a novel, next-generation dual BAFF/APRIL inhibitor in preclinical development, and MAU868, a monoclonal antibody designed to neutralize BK virus infection. For more information, please visit: www.veratx.com. Our values are the cornerstone of our culture. Our values guide everything we dofrom how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases. Position Summary
The Associate Director, Clinical Scientist will report to the Senior Director, Clinical Development and will be responsible for the development, evaluation, planning, and execution of clinical studies, ensuring scientific integrity and the interpretation of study data within a clinical development program. Working closely with cross-functional teams, contributing to drug-candidate development projects in both early and/or late-phase clinical development. The Associate Director, Clinical Scientist reports to Sr. Director, Clinical Development. Responsibilities
Support or assist the Clinical Development lead for a program and/or contribute as a key member of the Clinical Study Team. Actively participates in program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings, and may contribute to collaborative activities with other departments. Maintain a strong understanding of therapeutic disease areas and drug candidates, including underlying disease biology, clinical manifestations, therapeutic standard practices, compound mechanisms of action, and the competitive drug landscape. Assist with the design and execution of clinical research studies for early and/or late-stage assets, contributing to strategy development and proposals grounded in scientific literature. Author and/or review documents related to trials, such as medical monitoring plans, SAPs, informed consents, and clinical components of Clinical Study Reports. Support regulatory document development, quality reviews, and cross-functional comment resolution. Prepare information for stakeholder meetings (e.g., investigator meetings, governance, DMCs, regulatory authorities, scientific advisory boards, study steering committees) and may present data at external investigator meetings (SIV) and internal collaborations. Support clinical/medical data review, including safety monitoring activities and ensure patient safety in compliance with FDA, EMEA, ICH, and GCP guidelines, as well as applicable SOPs. Ensure consistent application of medical/clinical data review techniques across studies/programs and contribute to the drafting/updating/reviewing of medical/clinical data review plans for assigned studies. Qualifications
Bachelor's Degree in a related field and 5+ years of related scientific experience OR an advanced degree (Ph.D., Sc.D., M.S., M.P.H., PharmD) with 3+ years of related scientific experience. Experience in clinical research, with a focus on glomerular disease, autoimmune disease, or nephrology is a plus. Strong ability to critically analyze, interpret, and summarize data in a clear, scientifically accurate manner. Well-developed interpersonal and communication skills, with experience collaborating across teams and building strong, positive relationships. Strong organizational skills with the ability to manage multiple competing priorities in a fast-paced environment. High attention to detail and strong project management skills. Solid understanding of scientific writing principles, with the ability to communicate complex information clearly and concisely. Proficient in scientific writing tools (e.g., Microsoft Office suite, document management systems, reference management software) and ability to quickly learn new software applications. Vera Therapeutics Inc. is an equal-opportunity employer. Vera Therapeutics is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $ - $. The exact base pay offered will depend on factors including geography, qualifications, skills, and experience. At Vera, base pay is only one part of total compensation, which may include an annual performance incentive bonus, new hire equity, and ongoing performance-based equity, as well as benefits (medical, dental, vision, 401k match, flexible time off, and holidays). Notice to Recruiters/Staffing Agencies
Recruiters and staffing agencies should not contact Vera Therapeutics through this page. All recruitment vendors are prohibited from contacting our hiring managers, executives, or employees without a fully executed written agreement. Fraud Alert
Your personal information and online safety are a top priority. Please apply through our official career page at https://veratx.com/careers/. Recruiters will contact you using the veratx.com domain, and we will never request payments or sensitive information. If unsure, email human resources. Seniority level
Mid-Senior level Employment type
Full-time Job function
Health Care Provider
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