Altasciences
Drug Development
AssociateScientist,ADA
Neural analysis suggests this role is
optimal for Mid candidates.
“Associate Scientist, ADA at Altasciences. Skills: Scientific competency, Data analysis, Documentation. Tabulate and perform final data batch review. Perform multi-batch trend analysis”
Industry & Context.
Excellent troubleshooting skills
Requirement to have study protocols read and documented in English
What They're Looking For.
Must Have
College degree and/or University degree in Chemistry, Biochemistry, Immunology or applicable field, Knowledge of regulatory agency guidelines, Understand general SOPs, Good knowledge of GLP regulations, Good organizational skill, Highly flexible, Sense of urgency, Excellent troubleshooting skills, Client oriented, Attentive to details, Be able to easily read and understand study plans and protocols, Good communication both written and verbal in French & English
Nice to Have
Experience in regulated clinical and/or preclinical studies
What You'll Do.
Tabulate and perform final data batch review
Perform multi-batch trend analysis
Complete study documentation
Approve Memo to File or SOP/Protocol/Study Plan deviations
Provide report and/or final results within study timelines
exception or events are reflected
Assure analysis conducted are reported and accurate
Assist in writing validation and analytical plans/reports
Provide comments and/or recommendations
Assist for planning sample analysis
Maintain timeline and scheduling commitments
Perform ordering of reagents
Verification of inventory
Perform literature searches
Draft work plans for assay development
Assist with evaluation of risk and costing
Perform laboratory bench work for method development or validation
Interpretation of results
Documentation/tabulation of data
Troubleshooting when required
Keeps BPI and/or Senior Scientist involved
review and update method SOP
Support responses to QA reports
Provide feedback on progress
Assist in sponsor teleconferences
Conduct all work in compliance with applicable SOPs
Observes all company guidelines and policies
Respecting Health and Safety standards
How You'll Work.
Team & Collaboration
Keeps BPI and/or Senior Scientist involved through ongoing communications; Provide feedback on progress; Assist in sponsor teleconferences
Communication Scope
Good communication both written and verbal in French & English
Process & Methodology
Maintain timeline, Scheduling commitments
Full Job Description
**Your New Company!** At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team! Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences. We are better together and together We Are Altasciences. **About The Role** The Associate Scientist, ADA is the right hand help for the senior scientist. As such their responsibility is mainly to assist the senior scientist with tasks based on scientific competency and training. Based on competencies the Associate Scientist may be assigned as BPI. **What You’ll Do Here** * Tabulate and perform final data batch review by performing multi-batch trend analysis, completing all study documentation as required including approving of Memo to File or SOP/Protocol/Study Plan deviations where appropriate. * Provide report and/or final results within study timelines and ensure any deviation, exception or events are reflected as appropriate and assure that all analysis conducted are reported and accurate. * Assist in writing validation and analytical plans/reports and provide comments and/or recommendations, as needed, for the bioanalytical portions of preclinical and clinical protocols, study plans, laboratory manuals, Data Transfer Agreements, and/or other document. * Assist for planning sample analysis by maintaining timeline and scheduling commitments. * If assigned, perform the ordering of reagents, materials and if assigned verification of inve
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