MD or MD/PhD in a relevant discipline, preferably neurology., Minimum of 6 years of industry experience in neurology clinical development., Proven leadership skills and effective communication abilities., Experience in preclinical and clinical study design and execution..
Key responsabilities:
Provide scientific and medical leadership for preclinical and clinical neurology programs.
Establish relationships with thought leaders and represent the company at conferences.
Contribute to the development of clinical documents and regulatory submissions.
Mentor junior team members and support cross-functional collaboration.
Report This Job
Help us maintain the quality of our job listings. If you find any issues with this job post, please let us know.
Select the reason you're reporting this job:
BlueRock Therapeutics is a leading engineered cell therapy company with a mission to develop regenerative medicines for intractable diseases. BlueRock Therapeutics’ cell+gene platform harnesses the power of cells to create new medicines for neurology, cardiology, and immunology indications.
BlueRock Therapeutics’ cell differentiation technology recapitulates the cell’s developmental biology to produce authentic cell therapies, which are further engineered for additional function. Utilizing these cell therapies to replace damaged or degenerated tissue brings the potential to restore or regenerate lost function.
BlueRock’s culture is defined by scientific innovation, the highest ethical standards and an urgency to bring transformative treatments to all who would benefit. The company strives to be a top employer of scientific talent, empowering every member of the team to make meaningful and lasting contributions to the burgeoning field of regenerative medicine.
Become a BlueRocker! We are expanding our BlueRock team at all locations. Contact us via LinkedIn or our website to learn about rewarding career opportunities.
It continues to be an exciting time for BlueRock Therapeutics as the company advances cutting edge cellular therapies to positively impact patients’ lives across multiple disease areas.
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 Senior Medical Director Neurology will be charged with providing scientific and medical leadership and support for BlueRock’s neurology programs. Reporting to the Senior Vice President Clinical Development, this role will work closely with program leads and other subject matter experts to expand and execute on the company’s development pipeline. The successful candidate will be a clinical and scientific leader and resource, and they will support relationships and activities within BlueRock and externally with BlueRock partners.
The successful candidate will be a clinician scientist with both an interest and experience in preclinical as well as clinical stage development programs. They will build and maintain strong collaborative efforts with both internal and external partners and will provide guidance to research teams and IND-enabling and clinical-stage activities. They will contribute to highly productive, cross-functional development teams (such as research, regulatory, CMC, clinical development, clinical operations, and IP) within a dynamic matrixed environment. The position will be based in Cambridge, Massachusetts, with the potential to be hybrid or remote.
Responsibilities:
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
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
Minimum Requirements:
MD or MD/PhD in a relevant discipline is required (neurology strongly preferred)
Industry experience in neurology clinical development required
Minimum of 6 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
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
#LI-AL1
Required profile
Experience
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.