Associate Medical Director, Neurology

Medical DirectorMedical DirectorFull TimeRemote

Location

United States

Posted

19 days ago

Salary

Not specified

No structured requirement data.

Job Description

BlueRock is recruiting a key member of the Clinical Development group to support and direct preclinical, translational IND-enabling, and clinical development activities of the neurology programs. In this newly created role, the Associate Medical Director Neurology will be charged with providing scientific and medical leadership and support for BlueRock’s neurology programs. 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

Job 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
  • Target Base Salary: $215,000 - $253,200

Benefits

  • Winner of Boston Business Journal's Best Places to Work (Mid-size Company) 2023
  • Winner of Comparably's Award for Best Company for Diversity 2022
  • Winner of Comparably's Award for Best Company for Women 2022
  • Winner of Comparably's Award for Best CEO 2022
  • Ranked in the top 5% of companies for Overall Culture on Comparably
  • Engineering Department ranked in the top 5% of companies for Overall Culture on Comparably

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