
1001 - 5000 employees
Founded 1998
🧬 Biotechnology
💊 Pharmaceuticals
💰 Private Equity Round on 2017-06
Biotechnology • Pharmaceuticals
Altasciences is a forward-thinking, mid-size early phase contract research organization located in Canada and the U. S. , catering to biopharmaceutical companies of all sizes. The company specializes in offering a flexible approach to early drug development, with services that include preclinical safety testing, clinical pharmacology from Phase I to Phase II, bioanalysis from preclinical to Phase IV, as well as research and manufacturing analytical services. Altasciences is committed to accelerating early-phase drug development, ensuring seamless transitions from lead candidate selection to proof of concept and beyond, thereby delivering impactful results with a personal touch.
🔥 2 minutes ago
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1001 - 5000 employees
Founded 1998
🧬 Biotechnology
💊 Pharmaceuticals
💰 Private Equity Round on 2017-06
Biotechnology • Pharmaceuticals
Altasciences is a forward-thinking, mid-size early phase contract research organization located in Canada and the U. S. , catering to biopharmaceutical companies of all sizes. The company specializes in offering a flexible approach to early drug development, with services that include preclinical safety testing, clinical pharmacology from Phase I to Phase II, bioanalysis from preclinical to Phase IV, as well as research and manufacturing analytical services. Altasciences is committed to accelerating early-phase drug development, ensuring seamless transitions from lead candidate selection to proof of concept and beyond, thereby delivering impactful results with a personal touch.
• Evaluate clinical pathology data and prepare reports for nonclinical safety studies. • Support Study Directors in addressing clinical pathology related data and issues with sponsors. • Support client development through discussions with sponsors about study goals and designs. • Implement/support company-wide scientific initiatives involving the Clinical Pathology department as assigned. • Support continuing development of Study Directors and other Safety Assessment personnel. • Other duties as assigned
• D.V.M. (or Equivalent as listed by AVMA ECFVG) required • MS/MVSc/MSc, and/or Ph.D. preferred • Minimum 1-4 years experience as a Veterinary Clinical Pathologist (as board eligible trainee or board certified), ideally with pharma, biotech, and/or CRO experience. • DVM, Diplomate ACVP, ECVP in Veterinary Clinical Pathology • Ability to utilize Microsoft Office and pathology data management systems. • Proficiency in both written and verbal English; ability to read, analyze, and interpret common scientific and technical journals; ability to respond to common inquiries or complaints from customers or regulatory agencies; and, ability to effectively present information to clients, management, and public groups. • Ability to utilize appropriate mathematical concepts for interpreting scientific studies. • Additional skills required include, but are not limited to: general reading, writing, and verbal communication skills; and skills in scientific writing or electronic publishing.
• Health/Dental/Vision Insurance Plans • 401(k)/RRSP with Employer Match • Paid Vacation and Holidays • Paid Sick and Bereavement Leave • Employee Assistance & Telehealth Program
Apply Now🔥 44 minutes ago
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