Provide expert scientific and medical support and leadership to both preclinical and clinical stage BlueRock programs
Support development and progression of a robust BlueRock neurology pipeline
Medical monitoring and clinical review of active programs and studies
Establish strong relationships with thought leaders in the field
Represent the company in the neurology space both internally at meetings and externally, including global conferences.
Support the neurology pipeline by contributing to the assessment of potential new products or programs
Work with cross-functional teams, and contribute to strong, collaborative efforts to strengthen internal capabilities
Lead, contribute to, and provide oversight to development of clinical documents
Contribute to the analysis, interpretation and reporting of preclinical and clinical data
Provide clinical and scientific content and detailed review for regulatory documents, and contribute to the overall strategy in regulatory submissions and interactions
Provide strategic programmatic input through interaction with the development leadership team
Provide mentorship and support to more junior team members
Requirements
MD or MD/PhD in a relevant discipline is required (Neurology required)
Industry experience in neurology clinical development required
Minimum of 2+ years of experience, or a combination of relevant education and experience
Proven ability to lead teams by example and promote company culture
Effective communicator with excellent verbal and written communication skills
Interest and experience in preclinical/early development stage programs
Experience in design and execution of clinical studies
Knowledgeable in drug safety, compliance and cGMP
Ability to analyze, interpret, summarize and clearly communicate scientific data
Experience with clinical review software such as elluminate
Ability to work independently
Strong judgement and decision-making skills
Experience with and understanding of regulatory requirements drug development, and excellent regulatory writing skills
Ability to collaborate cross-functionally and with external stakeholders
Experience in cell or gene therapy is a strong plus
Benefits
Equal Opportunity Workplace
Support for differences and diversity
Disability-related accommodation during recruitment process