As an LC-MS Scientist II, you will manage bioanalytical studies, client communication, report writing, and adherence to GLP regulatory guidelines, collaborating with a team in a laboratory setting.

The Research Associate II will support laboratory operations, data collection, maintain equipment, assist with method development, and review quality control data.

Perform bench experiments, validation and sample analyses following SOPs, GLP/GCP. Maintain accurate documentation, complete supplementary forms, follow health and safety standards, and communicate quality issues to management.

The Study Support Specialist assists with study event designs, maintains study calendars, ensures compliance with protocols, and communicates with clinical teams.

The Quality Control Associate II ensures quality control of clinical trial data, assists in audits, mentors team members, and tracks errors while maintaining compliance with protocols.

The Screening Supervisor manages the screening team for clinical trials, ensuring compliance with protocols and coordinating schedules, training, and documentation responsibilities.

The Study Supervisor will oversee study procedures, coordinate teams, ensure compliance with guidelines, and assist with data collection in a research environment.

Develop and execute digital marketing campaigns and materials (social, e-blasts, ads, videos, infographics), manage content and social calendar, assist SEO and analytics, ensure brand consistency, coordinate vendors, and support marketing operations and collateral maintenance.

As a Principal Research Scientist, you will lead technical expertise in LC-MS/MS, ensuring compliance with GLP, overseeing method validation, and training staff while interacting with clients and managing projects.

The Senior Lead Data Manager oversees data management activities throughout clinical studies, ensuring quality control, managing client relationships, and mentoring team members. Responsibilities include developing documentation, coordinating with database developers, and participating in process improvement initiatives.

Join Altasciences as an LCMS Scientist to assist in drug therapy development and manufacturing, making a global health impact.

Plan and schedule staff resources to meet clinical trial activity needs by reviewing protocols, developing and approving schedules, tracking availability, coordinating training, communicating with clinical teams and placement agencies, and performing related administrative tasks.

The Marketing Manager collaborates with internal teams to develop integrated marketing strategies, manage projects, and support brand awareness and lead generation for Preclinical services.

The HR Business Partner guides managers on HR practices, manages employee relations, and implements HR strategies to meet business goals.

The Scientist will manage and conduct method development, validation, and sample analysis studies while ensuring quality and compliance with regulations. They will mentor and support team members, interact with clients, and organize complex data reporting.

The Senior Biostatistician leads statistical analysis in clinical trials, mentors other biostatisticians, and ensures high-quality deliverables according to regulatory standards.

The Strategic Partnership Manager is responsible for managing key client relationships, ensuring satisfaction, facilitating information sharing, and improving processes to optimize drug development objectives.