
1001 - 5000 employees
Founded 1998
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
đź’° Private Equity Round on 2017-06
Healthcare • Consulting • Logistics
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.
🔥 15 hours ago
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1001 - 5000 employees
Founded 1998
🏥 Healthcare
đź’Ľ Consulting
📦 Logistics
đź’° Private Equity Round on 2017-06
Healthcare • Consulting • Logistics
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.
• Serve as a Clinical Pathologist on nonclinical safety studies • Evaluate clinical pathology data and prepare GLP and nonGLP reports • Collaborate with Study Directors, Anatomic Pathologists, and other relevant personnel • 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 or support company-wide scientific initiatives involving the Clinical Pathology department • Support continuing development of Study Directors and other Safety Assessment personnel • Perform other duties as assigned
• D.V.M. (or Equivalent as listed by AVMA ECFVG) required • 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, JCVP, 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 • Ability to effectively present information to clients, management, and public groups • Ability to utilize appropriate mathematical concepts for interpreting scientific studies • Continuing education in toxicology and pathology may be included in training needs • Continual GLP training • General reading, writing, and verbal communication skills • Skills in scientific writing or electronic publishing • Preferred: expertise in clinical pathology; knowledge of current scientific and industry specific literature; ability to successfully operate independently with minimal guidelines; excellent interpersonal and communication skills
• 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 • Training & Development Programs • Employee Referral Bonus Program
Apply Nowđź•’ September 20
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