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Zoetis

Parasitology - Clinical Research

Zoetis, Kalamazoo, Michigan, United States, 49006

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Overview

Join to apply for the Parasitology - Clinical Research role at Zoetis. Global Clinical Research and Development (VMRD) Veterinary Medicine Research & Development. Position responsibilities

The successful applicant embodies Zoetis' Core Beliefs: Our Colleagues Make The Difference, Always Do The Right Thing, Customer Obsessed, Run It Like You Own It, and We Are One Zoetis. Within US Clinical Operations, the candidate will be assigned to one or more Project Teams and will have the following duties and responsibilities: Prepare study protocols, amendments, deviations, data capture forms, electronic data capture systems, test article documentation and study reports in preparation for submission to regulatory agencies. Collaborate with multiple internal partner groups to plan, coordinate, conduct, analyze, and report studies. Develop training materials and conduct training of Investigators and other study site personnel. Coordinate animal related study activities (i.e. clinical sampling, test material administration and clinical observations). Serve as the principal communication link between the Sponsor and study sites. Maintain study files in accordance with SOPs and regulatory requirements. Implement and execute data management processes including paper and electronic data capture, entry, review, tracking, and verification utilizing electronic tools and centralized data management systems. Prepare study files, author study reports and review technical section summaries for submission to regulatory agencies (FDA, EMA, EPA). Lead multi-functional team(s) serving as a project team member or clinical team lead. Contribute to, review and/or author manuscripts for journal publication. Present results, as needed, both internally and to external scientific audiences. Travel: approximately 10 - 40% on an annual basis. Variable, depending upon project status. Education and experience

Educational Background: Work Experience/Skills: Minimum: Five years' experience as a clinical study coordinator/monitor or in research/product development in the animal health pharmaceutical industry Experience in the study design and execution of parasitology laboratory clinical studies Familiarity with parasitology study designs and models as well as regulatory guidance/expectations for the conduct and execution of parasitology studies Previous experience with preparation of regulatory submissions for FDA, EPA and/or EMA for product registration Previous experience working with veterinary clinics and/or research facilities Experience with Good Clinical Practice and/or Good Laboratory Practices Ability to work both as a member of a team and independently in a self-directed and self-motivated manner Excellent skills in organizing, planning, time management, quality, attention to detail Well-developed critical thinking skills with the ability to learn on the fly and problem solve Excellent interpersonal skills with very good written and oral communication skills Competence with Microsoft Office Products (Outlook, Word, Excel, OneNote, Teams) Experience in configuring studies in an electronic data capture platform/ eClinical software Experience and interest in the conduct and leadership of companion animal clinical field studies Education and clinical experience in the field of veterinary technology Competence with electronic data capture, eClinical software or remote communication tools MS or MPS in Veterinary Parasitology, Veterinary Biomedical Science or Veterinary Public Health About Zoetis

At Zoetis, our purpose is to nurture the world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We offer competitive healthcare and retirement savings benefits, along with an array of benefits, policies and programs to support employee well-being. Global Job Applicant Privacy Notice

Seniority level Mid-Senior level Employment type

Full-time Job function

Other, Research, and Science Industries

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