Research Associate, Bioanalytical

Visterra•Waltham, MA

5d•$92,000 - $100,000•Onsite

About The Position

Visterra, Inc., is seeking a highly motivated Research Associate with experience in immunology, large molecule/bioanalytical techniques to perform laboratory activities and experiments related to the development and scientific qualification of bioanalytical methods for preclinical/clinical programs. Reporting to a Scientist/Senior Scientist in the Bioanalytical department, this individual will play a key technical role in the development, qualification and analysis for non-regulated/exploratory methods and study samples in support of drug development candidates. They will perform experiments to support IND filings and early pre-clinical development. The ideal candidate should have a B.S. degree in biology, molecular/cellular biology, immunology, or related field and a minimum of one year “at the bench” research experience (Laboratory “labs” as part of undergraduate training are excluded). The successful candidate will be a collaborative team player, a critical thinker, a clear communicator, excellent at documentation, and one that thrives in a fast-paced environment. The ideal candidate must possess exceptional proficiency in pipetting, using both single-channel and multi-channel pipettes. Precision, accuracy, and efficiency in liquid handling are essential for this role. This is a full-time, on-site laboratory-based position located at Visterra’s facility in Waltham, MA. Visterra is a clinical stage biotechnology company committed to developing innovative antibody-based therapies for the treatment of patients with kidney, immune-mediated and other hard-to-treat diseases. Our proprietary technology platform enables the design and engineering of precision antibody-based product candidates that specifically bind to, and modulate, key disease targets. Applying this technology to disease targets that are not adequately addressed by traditional therapeutic approaches, we are developing a robust pipeline of novel therapies for patients with unmet needs. Visterra’s pipeline has multiple clinical-stage assets and one approved therapeutic, sibeprenlimab. As a member of the Otsuka family of companies, we are uniquely positioned as a small, dynamic, nimble and innovative organization where individuals and teams are empowered to make big impacts – while benefiting from the support, strength, stability and long-term perspective of a 100-year-old global company. Visterra has approximately 105 employees and is located in Waltham, Massachusetts. Visterra provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Requirements

A bachelor’s degree in molecular/cellular biology, immunology, chemistry or related scientific field and a minimum of one year “at the bench” (this excludes laboratory courses during undergraduate training).
Hands-on experience in one or more of the following areas: Enzyme-Linked Immunosorbent Assay (ELISA). Electrochemiluminescence immunoassay (ECLIA). Cell-based assays and flow
Aseptic technique and culture of mammalian
Strong time management and organizational skills, attention to accuracy and detail, and the ability and willingness to multi-task as needed.
A detail-oriented and organized individual with strong communication skills (written and oral).
A highly motivated, inquisitive individual who thrives in a fast-paced and dynamic research environment.
An individual who is adaptable and able to quickly learn new concepts and experimental
Proficient use of commonly used software for data analysis (Excel).
Moderate skill using Microsoft Office (Powerpoint etc.)
Limited travel (< 5%) may be required to attend conferences and industry

Responsibilities

Conduct experiments to develop large molecule bioanalytical methods.
Perform routine care for equipment/platform to support bioanalytical methods.
Conduct method qualification experiments.
Collaborate, as needed, with external vendors for the transfer of primarily ELISA/ECL based PK, ADA and biomarker assays to support large molecule drug candidates.
Perform internal testing of preclinical samples.
Maintain inventory of critical reagents for Bioanalysis.
Develop an understanding of fundamental principles, theories, and concepts in bioanalysis.
Develop a knowledge of regulatory requirements, including GLP, GCP, ICH and other applicable guidelines for Bioanalytical development in support of clinical trials.
Analyze and summarize key data sets and results for internal review, including written technical reports and oral presentations.
Operate, collaborate, and communicate effectively in a team-oriented, cross-functional organization.
Other duties and responsibilities as required by departmental and business need.