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Research Pathologist

Role overview

Qualifications

  • D.V.M. (or Equivalent as listed by AVMA ECFVG®)
  • Minimum of 5 years of toxicologic pathology experience in a GLP environment
  • Diplomat of A.C.V.P. or J.C.V.P. or E.C.V.P. or R.C.P.
  • Proficient in MS Word, Excel, Outlook and Power Point

Responsibilities

  • Perform duties of a study pathologist or peer reviewer on preclinical toxicology studies
  • Write comprehensive report narratives detailing all test article effects
  • Provide training, technical guidance, and leadership to laboratory staff
  • Maintain an up-to-date knowledge in toxicologic pathology

Key facts

Hard skills

Other skills

  • Report Writing
  • Mentorship
  • Communication
  • Social Skills
  • Multitasking
  • Self-Motivation

About the company

Altasciences logo

Altasciences

  • Clinical Research (CRO)
  • Large
  • 1,001–5,000
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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Job description


About The Role

Perform duties of a study pathologist or peer reviewer on preclinical toxicology studies. Diagnose presence and stage of disease/toxicity using laboratory techniques and patient specimens. Study the nature, cause, and development disease/toxicity.


You'll Do Here

  • Perform macroscopic and microscopic tissue evaluations and interpretation of assigned studies.
  • Assist with necropsy supervision and gross pathology interpretation. Guiding of personal staff for sample collection and technical development.
  • Write comprehensive report narratives detailing all test article effects.
  • Enter pathology findings in data capturing system.
  • As needed, work with study directors to ensure data is accurately integrated into study reports.
  • Provide training, technical guidance, and leadership to laboratory staff.
  • Maintain an up-to-date knowledge in toxicologic pathology.
  • May serve as principal investigator for contract pathology work, participate in pathology working group (PWG) as an observer and serve as a consultant in pathology-related issues
  • May provide scientific expertise for experimental design and other aspects of research studies, as needed.
  • Act as pathology representative for important sponsors.
  • Provide mentorship (study scientific reviews) on assigned studies to less experienced pathologists.
  • Support establishment and or refinement of significant operational or scientific improvements within pathology.
  • Ability to build strong bonds with technicians to foster open, honest, and candid communications
  • Ability to multi-task and stay organized in a fast paced, changing environment.
  • Provide training, technical guidance and leadership to laboratory staff, pathology trainees, and less experienced pathologist.

What You'll Need to Succeed

  • D.V.M. (or Equivalent as listed by AVMA ECFVG®)
  • Minimum of 5 years of toxicologic pathology experience in a GLP environment
  • Diplomat of A.C.V.P. or J.C.V.P. or E.C.V.P. or R.C.P.
  • MS Word, Excel, Outlook and Power Point
  • Ability to read and interpret technical documents and industry specific manuals.
  • Ability to write advanced reports and correspondence.

Other Requirements:

  • Excellent verbal and written communication skills.
  • Well developed interpersonal skills are required.
  • Personal/professional integrity and proven discretion in handling confidential information.
  • Ability to develop strong trusting relationships in order to gain support and achieve results.
  • Capable of managing multiple conflicting priorities.
  • Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.
  • Relevant industry experience a plus.

What We Offer

The salary range estimated for this position is $170,000 - $210,000.  Please note that 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

Altasciences' Incentive Programs Include:

  • Training & Development Programs
  • Employee Referral Bonus Program 

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