Altasciences · 2 days ago

Associate Scientist, DCA

Columbia, MD

Full-time

Onsite

Mid Level

3+ years exp

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Responsibilities

Oversee and maintain study conduct according to GLP regulations and as described in the appropriate oversight documents (ex: SOPs, Method Validation Plan (MVP), Protocol, and Analytical Method).

Serve as a Contributing Scientist for dose concentration analysis phase of the study when necessary.

Serve as a Responsible Scientist for method validations when necessary.

Critically analyze study or project data under supervision and compile into reports for internal and client-sponsored GLP and non-GLP preclinical drug studies.

Collect and review dose concentration analysis data according to the Contributing Scientist or Principal Investigator and the appropriate oversight documents (ex: MVP, Protocol, Analytical Method, SOPs).

Write and peer review technical documents (ex: MVPs, SOPs, study forms, and data reports).

Assist with the development and implementation of new assays and projects to support internal and client-sponsored studies.

Assist with responding to inquiries from clients and other relevant parties regarding scientific aspects of projects.

Respond to audits of dose concentration analytical data.

Qualification

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Technical WritingComputer SkillsGLP KnowledgeLC TechniquesUV/Vis AssaysEffective CommunicationPublic Speaking

Required

B.S. +3 years or M.S. +1 year of experience or an equivalent combination of education and experience in performing laboratory-based assays related to analytical chemistry

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, software manuals, study documents, and procedure manuals

Advanced technical writing with the ability to write and present scientific articles and complex topics to people of different backgrounds and education levels

Ability to speak effectively before groups of customers or employees of the organization

Intermediate to advanced computer skills

Experience with GLP advanced knowledge of LC techniques and UV/Vis assays preferred