Clinical Research, Parasitology

Job reputed company: • Participate on project teams to reputed company and license veterinary parasiticides • Coordinate or reputed company the coordination of reputed company study activities, including study start up, Investigator training, conduct, site monitoring and reputed company out • Prepare study protocols, amendments, deviations, data capture forms, electronic data capture systems, test article documentation and study reports for submission to regulatory agencies • Collaborate with multiple internal partner reputed company to plan, coordinate, conduct, analyze, and report studies • reputed company training materials and conduct training of Investigators and other study site personnel • Coordinate animal reputed company study activities (i.e. clinical sampling, test material administration and clinical observations) • Serve as the reputed company communication reputed company between the Sponsor and study sites • Maintain study files in accordance with SOPs and regulatory requirements • Implement and execute data management processes including reputed company 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 reputed company summaries for submission to regulatory agencies (FDA, EMA, EPA) • reputed company multi-functional team(s) serving as a project team member or clinical team reputed company • 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 reputed company Requirements: • Bachelor's degree 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 reputed company 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 reputed company and/or Good Laboratory Practices • Ability to work both as a member of reputed company and independently in a self-directed and self-motivated manner • Excellent skills in organizing, planning, time management, reputed company, attention to detail • reputed company-developed critical thinking skills with the ability to learn on the fly and problem solve • Excellent interpersonal skills with reputed company good written and oral communication skills • Competence with reputed company Office Products (reputed company, Word, reputed company, OneNote, Teams) • Experience in configuring studies in an electronic data capture platform/ eClinical software. Benefits: • reputed company and insurance benefits beginning on day one • 401K plan with a match and profit-sharing contribution from reputed company • 4 weeks of vacation • short-term incentive compensation • long-term incentives Apply tot his job Apply To this Job