About The Role
As an Associate Scientist you will provide technical and scientific leadership in the area (e.g., biomarker, pharmacokinetic, ligand assay). Plan and execute projects, and identify and acquire the necessary facilities, equipment and procedures for research projects by performing the below duties.
What You'll Do Here
Oversee and maintain study conduct according to GLP regulations and as described in the appropriate oversight documents (ex: SOPs, Study Protocol, and Analytical Study Plan).
Under supervision, critically analyze study or project data and compile into reports for internal and client sponsored GLP and non-GLP preclinical drug studies.
Collect and review molecular biology data according to the Contributing Scientist or Principal Investigator and the appropriate oversight documents (ex: Protocol, Analytical Study Plan, SOPs).
Write and peer review technical documents (ex: Protocols, SOP’s, validation plans, 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.
What You'll Need to Succeed
BS with 3 years or MS with 1 year of experience or PhD, or an equivalent combination of education and experience in performing laboratory-based assays related to immunology, molecular biology, and/or cell biology/biochemistry/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 Math Skills.
Advanced technical writing and good oral communication skills; the ability to learn and understand complex theories and applications; the ability to read, analyze, and interpret complex documents; and the ability to work independently with minimal supervision.
Experience with GLP, knowledge of bioanalysis, and familiarity with analytical equipment e.g., chromatography, Luminex, RT-PCR equipment, preferred
Work Authorization & Sponsorship:
Applicants must be legally authorized to work in the United States. Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position. All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.
What We Offer
The pay range estimated for this position is $80,000 annually. Please note that hourly rates/salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.
Benefits
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
Telework when applicable.
Altasciences’ Incentive Programs Include:
Training & Development Programs
Employee Referral Bonus Program
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Skills Required
- BS degree with 3 years of relevant laboratory assay experience, MS degree with 1 year of experience, or PhD; equivalent education and experience may be accepted.
- Laboratory-based assay experience related to immunology, molecular biology, cell biology, biochemistry, and/or chemistry.
- Ability to interpret safety rules, operating instructions, software manuals, study documents, and procedure manuals.
- Advanced technical writing and ability to write and present scientific articles and complex topics.
- Effective oral communication and presentation skills.
- Intermediate to advanced mathematics skills.
- Ability to learn complex theories, analyze complex documents, and work independently with minimal supervision.
- Experience with GLP.
- Knowledge of bioanalysis.
- Familiarity with analytical equipment such as chromatography, Luminex, and RT-PCR equipment.
- Legally authorized to work in the United States without current or future employer sponsorship.
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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