Scientist, Bioanalytical Development

Visterra•Waltham, MA

2d•Onsite

About The Position

The Scientist, Bioanalytical Development is responsible for performing laboratory activities and experiments related to the development and scientific qualification of bioanalytical methods for preclinical/clinical programs to assess PK, ADA and PD in preclinical and clinical samples. The Scientist, Bioanalytical Development will be responsible for activities related to the bioanalytical method development and qualification for non-regulated/exploratory methods and sample analysis from preclinical studies in support of drug development candidates. Reporting to the Associate Director in Bioanalytical Development, this role will be responsible for the execution of experiments to support IND filings / preclinical development as well as clinical method development. They may also oversee the activities of a research associates and perform project management activities for out-sourced methods including vendor management. Visterra is seeking a flexible candidate with a working knowledge of large molecule/biologics analytical techniques and laboratory skills. The primary focus will be developing and performing bioanalytical methods for programs in preclinical and clinical development, documenting the methods used and summarizing the data collected. This individual will be responsible for the execution and documentation of experiments to develop bioassays and the empirical evaluation of custom reagents to support preclinical/clinical method development. This is a full-time laboratory position based in Visterra’s facility in Waltham, MA.

Requirements

A minimum of 5 years of working experience, including hands-on laboratory experience in the bioanalysis or biotechnology industry.
An M.S. or Ph.D. in Immunology, Biology, Biochemistry, or related field is preferable, although candidates with a Bachelor of Science (BS) degree with significant research experience are also encouraged to apply
Experience with ligand binding method development using ELISA and MSD.
Working experiences with biologics.
Proven experience in the development and validation of regulated bioanalytical method assays for pharmacokinetic, pharmacodynamic and immunogenicity evaluation.
Experience with summarizing data in slides and reports.
Experience with vendor management and project management.
Knowledge of regulatory requirements, including GLP, GCP, ICH and other applicable guidelines for Bioanalytical development in support of clinical trials.
Extensive experience with a broad range of bioanalytical platforms including ELISA, MSD and Flow Cytometry and techniques including bridging, direct, indirect, and competitive assays.
Ability to manage a research associate as a direct-report, including assigning and reviewing tasks and mentoring and coaching.
Strong time management and organizational skills, attention to accuracy and detail, and the ability and willingness to multi-task as needed.
This individual will be highly analytical, goal-oriented, and timeline sensitive while maintaining high quality standards.

Responsibilities

Develop ligand binding methods including pharmacokinetic (PK), immunogenicity (ADA) and pharmacodynamic (PD) assays.
Design and independently execute experiments to select/identify appropriate bioanalytical reagents.
Oversee and perform sample analysis from preclinical and clinical studies.
Design and implement specialized in vitro studies designed to enhance mechanistic understanding of drug development candidates as needed on development programs.
Analyze data and trouble shoot assay development activities.
Write reports summarizing data and methods.
Manage and oversee activities of Research Associates.
Implement innovative technologies which offer pragmatic enhancements to the bioanalytical department.
Manage ongoing bioanalysis at external vendors to support large molecule drug candidates.
Negotiate CRO contracts and SOWs; from approval to execution.
Review, edit, and finalize method validation protocols, amendments, and reports, ensuring that documents meet project timelines, expectations, and deliverables, as well as Visterra’s global regulatory and compliance requirements.
Other duties and responsibilities as required by departmental and business needs.
Travel as needed to attend conferences, events and vendor site visits.