Associate Scientist, PK & Biomarker

Posted 2 Days Ago
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Laval, QC, CAN
In-Office
Mid level
Information Technology • Analytics • Biotech
The Role
Assist senior scientist with bioanalytical tasks including data review, multi-batch trend analysis, report generation, method development/validation, sample analysis, documentation, inventory/order management, QA support, sponsor communication, and compliance with SOPs, GLP and GCP. Bilingual French/English communication required.
Summary Generated by Built In

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, PK & Biomarker 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, PK & Biomarker 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 inventory. Perform literature searches and draft work plans for the development of assays as assigned.

  • Assist with evaluation of risk and costing. Based on training and competency, perform laboratory bench work for method development or validation, interpretation of results, documentation/tabulation of data and troubleshooting when required.

  • Keeps BPI and/or Senior Scientist involved through ongoing communications.

  • Write, review and update method SOP as needed Support responses to QA reports Assigned by management on studies and tasks based on scientific competency and training (can include method development, validation or sample analysis projects).

  • Provide feedback on progress and assist in sponsor teleconferences as required.

  • Conduct all work in compliance with applicable SOPs, GCPs, GLPs and observes all company guidelines and policies.

  • Respecting Health and Safety standards in terms of personal protection, laboratory maintenance, and work procedures.

What You’ll Need to Succeed

  • Ideally College degree and/or University degree in Chemistry, Biochemistry, Immunology or applicable field.

  • Preferred experience in regulated clinical and/or preclinical studies with typically 3 year of experience.

  • Knowledge of regulatory agency guidelines and must understand general SOPs and have good knowledge of GLP regulations.

  • Good organizational skill.

  • Highly flexible.

  • Sense of urgency.

  • Excellent troubleshooting skills.

  • Client oriented, attentive to details.

  • Able to easily read and understand study plans and protocols.

  • Ability to coach/mentor people.

  • Good communication both written and verbal in French & English.

Altasciences strives to provide a French work environment for its employees in Quebec. Altasciences has taken all reasonable measures to avoid imposing the above language requirement. This requirement is essential for the position of Associate Scientist, PK & Biomarker in particular, but without limitation, for the following reason(s):

  • The requirement to have study protocols read and documented in English as required by industry regulatory agencies

What We Offer:

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:

  • Health/Dental/Vision Insurance Plans

  • 401(k)/RRSP with Employer Match

  • Paid Vacation and Holidays

  • Paid Sick and Bereavement Leave

  • Employee Assistance & Telehealth Programs

Altasciences' Incentive Programs Include:

  • Training & Development Programs

  • Employee Referral Bonus Program

  • Annual Performance Review

#LI-MB1

MOVING IN UNISON TO DELIVER A BIG IMPACT WITH A PERSONAL TOUCH

Altasciences is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, creed, sex, sexual orientation, gender identity, national origin, disability or any other protected grounds under applicable legislation. Reasonable accommodations for persons with disabilities during the recruitment process are available upon request. Join us at Altasciences!

Skills Required

  • College or University degree in Chemistry, Biochemistry, Immunology or related field
  • Experience in regulated clinical and/or preclinical studies (typically 3 years)
  • Good knowledge of GLP regulations and understanding of general SOPs
  • Good organizational skills
  • Flexible with a strong sense of urgency
  • Excellent troubleshooting skills
  • Client-oriented and detail-oriented
  • Ability to read and understand study plans and protocols
  • Ability to coach and mentor others
  • Strong written and verbal communication in French and English
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The Company
HQ: Laval, Quebec
1,832 Employees
Year Founded: 1995

What We Do

Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 25 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!

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