Zenas BioPharma

Biopharmaceutical

AssociateDirector,ClinicalScientist

$162–202k Boston, Massachusetts, United States
The Brief

“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.

Biopharmaceutical
Eligibility Requirements

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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