The QC Reviewer is responsible for ensuring accurate quality control of laboratory data and documentation while adhering to SOPs and regulatory requirements.

The Associate Scientist assists the senior scientist by performing data analysis, writing reports, managing sample analysis, and ensuring compliance with regulatory guidelines.

The Scientist PK & Biomarker manages studies, ensures compliance with protocols, mentors analysts, and oversees method validation and analysis while communicating effectively with clients.

The Quality Control/Data Entry Associate reviews screening documents, performs data entry into EDC systems, and maintains tracking tools to ensure data quality and timely resolution of queries.

The Marketing Manager will develop and execute integrated marketing strategies for Bioanalytical Services, collaborating with stakeholders and driving brand awareness and sales growth.

Develop and optimize bioanalytical methods using LC-MS, perform analysis, write SOPs, collaborate with teams, and stay updated on technologies.

The Quality Control Associate reviews and validates clinical trial data to ensure compliance with protocols and regulatory guidelines, identifies errors, and assists in scheduling appointments.

The Marketing Administrator manages day-to-day marketing operations, providing administrative support, maintaining marketing content, managing vendors, and preparing reports.

The Senior QA Auditor conducts audits of study-related activities for regulatory compliance, mentors staff, and reports findings to management. Responsibilities include maintaining audit documentation, process improvement, and regulatory training.

The Financial Analyst supports month-end closing, reconciliations, financial reporting, and internal controls implementation, ensuring compliance with GAAP.

The Supervisor, Husbandry manages colony facilities and staff, ensuring proper animal care, compliance with regulations, and training of employees.

The Research Associate performs technical procedures, operates laboratory equipment, collects specimens and data, and supports research studies while complying with SOPs and GLP standards.

As a Scientist, you'll manage drug therapy studies, ensuring quality and compliance with regulations, while mentoring analysts and communicating complex data effectively.

Assist in the Laboratory Sciences department with daily operations, maintain equipment, prepare materials for assays, and document laboratory records.

Assist with administrative and professional support for study progression including scheduling, reporting, and compliance checks under the guidance of Study Directors and Principal Investigators.

The QC Reviewer is responsible for quality control of laboratory data, ensuring compliance with SOPs, analyzing trends, and mentoring staff.

The Quality Control Associate II ensures quality control in clinical trials, maintains data confidentiality, and assists in audits while mentoring team members.

The Senior QA Auditor conducts audits to ensure compliance with GLP and regulatory standards, mentors staff, and recommends process improvements.

The Senior Manager, Data Management oversees data management operations, ensuring quality and compliance across clinical trials while leading a team and collaborating with cross-functional stakeholders.

As a Scientist at Altasciences, you will support laboratory operations, perform mass-spectrometry assays, maintain records and equipment, and ensure compliance with guidelines.