Altasciences

Drug Development

AssociateScientist,ADA

Laval, Quebec, Canada; Montréal, Quebec, Canada FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid candidates.

The Brief

“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.

Drug Development
Problems you'll solve

Excellent troubleshooting skills

Eligibility Requirements

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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