Senior Clinical Scientist, Neurology

Nice to have:

Strong clinical and scientific knowledge

Working knowledge of applicable clinical trial regulations/guidelines (ie, ICH, FDA, EMA guidelines) and good clinical practice (GCP)

Excellent communicator with strong interpersonal skills; ability to efficiently address conflict and build relationships with key partners and stakeholders

With guidance, act as a clinical scientist and clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs

With guidance, contribute to the design and execution of Phase 1-3 clinical trials for the assigned therapeutic programs

Develop clinical and scientific content for inclusion into the clinical development plan for assigned therapeutic programs

Collaborate in the writing and review of protocols/amendments, study-level consent forms, study plans, investigator brochures, study reports, ethics committee responses, and other clinical and regulatory documents

Contribute to the creation of case report forms, training materials and provision of protocol/therapeutic area training to members of the clinical study team and investigative site staff

Interact with principal investigators and opinion leaders to facilitate clinical trials research