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Ms In Clinical Experimental Therapeutics Jobs (NOW HIRING)

Crispr Therapeutics

Clinical Trial Associate

South Boston, MA · On-site

$36.50 - $49.75/hr

CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary ... Proficient in MS Excel, Word and PowerPoint. * Established ability to prioritize and manage ...

Tempus

$110K - $114K/yr

Clinical Genomics Scientist II Compensation: $110,000-$114,000 annually Remote US: Experienced ... D. in Molecular Biology, Genetics, or related scientific field or MS in Genetic Counseling from an ...

Crispr Therapeutics

Clinical Trial Associate

Boston, MA · On-site

$36.50 - $49.75/hr

Proficient in MS Excel, Word and PowerPoint. * Established ability to prioritize and manage ... CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility ...

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Senior Principal Scientist - Global Biologics, Swine

Kalamazoo, MI • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 13 days ago

Job description

POSITION RESPONSIBILITIES:
  • Design and conduct clinical studies and programs for swine vaccine projects, including hypothesis-driven study design, protocol development/writing, study monitoring (including potential animal observations), data analysis/interpretation, and report/technical section/regulatory dossier writing.
  • Develop infectious disease swine models in appropriate age animals for vaccine efficacy testing; understand normal swine health/behavior for vaccine safety testing.
  • Ensure studies are conducted per applicable requirements, including SOPs, corporate policies, and regulatory guidelines (Good Clinical Practice and Good Laboratory Practice; some GLP work may be required).
  • Collaborate cross-functionally (Clinical and Project teams) to define/track study progress, activities, timelines, and outcomes; address resource/time/budget constraints with Project Manager/Team Leader.
  • Collaborate with Regulatory Affairs for protocol approval and support submissions to global regulatory agencies.
  • Organize and manage multiple projects simultaneously and prioritize work.
  • Provide hands-on expertise at laboratory and field study sites.
  • Prepare internal/external presentations and publications.
  • Support development of colleagues in Clinical and Project teams.
  • Occasional travel required.
EDUCATION AND EXPERIENCE:
  • Minimum: DVM/VMD (or equivalent) with experience in swine health.
  • Preferred: 3+ years as a swine practitioner and/or swine production experience, and/or PhD/MS in swine health/production animal discipline, and/or animal health industry swine clinical development experience; demonstrated leadership and mentoring.
SKILLS/TOOLS:
  • Excellent written and verbal communication.
  • Working knowledge of MS Office (Outlook, Word, Excel, PowerPoint).
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