Associate Medical Director, Neurology
BlueRock Therapeutics
full-time
Posted on:
Location Type: Hybrid
Location: Cambridge • Massachusetts • United States
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Salary
💰 $215,000 - $253,200 per year
Job Level
About the role
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
MDMD/PhDneurology clinical developmentclinical studies designregulatory writingdata analysisdrug safetycGMPpreclinical developmentcell or gene therapy
Soft Skills
leadershipeffective communicationteam collaborationmentorshipjudgementdecision-makingindependencerelationship buildingstrategic inputinterpersonal skills