Zenas BioPharma
Biopharmaceutical
AssociateDirector,ClinicalScientist
“Associate Director, Clinical Scientist at Zenas BioPharma. Skills: Clinical Scientist, Clinical trials, Neurology. Contribute to scientific development. Contribute to execution of global clinical studies”
Industry & Context.
Willingness to travel 10–15%
What They're Looking For.
Must Have
Advanced scientific or clinical degree, 3 to 5 years clinical research experience, Experience in clinical trial conduct, Understanding of clinical development processes, Understanding of regulatory requirements, Understanding of global guidelines, Understanding of applicable SOPs, Excellent communication skills, Excellent technical writing skills, Experience drafting scientific content, Experience reviewing scientific content, Experience editing scientific content, Experience drafting clinical content, Experience reviewing clinical content, Experience editing clinical content, Ability to work effectively, Ability to work collaboratively, Ability to manage multiple priorities, Ability to drive sound results
Nice to Have
Prior experience supporting neurology clinical trials
What You'll Do.
Contribute to scientific development
Contribute to execution of global clinical studies
Contribute to development of core study documents
Contribute to review of core study documents
Perform ongoing review of clinical trial data
Perform ongoing interpretation of clinical trial data
Ensure quality of clinical trial data
Ensure completeness of clinical trial data
Ensure consistency of clinical trial data
Ensure protocol compliance of clinical trial data
Participate as member of cross-functional study teams
Ensure timely execution of clinical trial milestones
Ensure high-quality execution of clinical trial milestones
Clinical Scientist in study execution
Serve as key clinical science resource
Serve as subject matter expert
Contribute to preparation of regulatory submissions
Contribute to authoring of regulatory submissions
Contribute to revision of regulatory submissions
Contribute to preparation of health authority responses
Contribute to authoring of health authority responses
Contribute to revision of health authority responses
How You'll Work.
Team & Collaboration
Cross-functional study teams; Global clinical programs
Communication Scope
Technical writing; Scientific content; Clinical content
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