The Senior Clinical Trial Manager oversees all operational aspects of clinical studies, ensuring compliance with regulatory requirements and managing project teams and vendors.
The Senior Medical Director will lead clinical development activities for pipeline products, providing medical leadership and collaborating with cross-functional teams to drive innovative treatment strategies.
The Senior Manager/Associate Director of Biostatistics will lead statistical activities across clinical studies, ensuring high-quality deliverables and contributing to regulatory submissions.
The Senior Director, Device Engineering will serve as the technical expert for combination products and drug delivery devices, leading device development and integration strategies.
This role offers a unique chance to lead pricing and contracting operations at Scholar Rock, managing GTN processes and shaping a growing team.
The Associate Director, Regulatory Strategy will develop and implement regulatory strategies for clinical programs, ensuring compliance and leading interactions with regulatory authorities.
The Associate Director/Director of Medical Operations will lead project management initiatives within Medical Affairs, ensuring effective collaboration and successful completion of key milestones.
The Senior Engineer, Downstream Manufacturing Science & Technology (MSAT) will lead technical efforts in monoclonal antibody downstream manufacturing, ensuring effective processes across a global network.
The Senior Director, Head of Clinical Quality Assurance will lead GCP quality strategy and oversight for clinical trials, ensuring compliance and operational excellence across biologics development.
The Senior Manager, Contracts will lead the drafting and negotiation of various biotechnology agreements while providing legal support across multiple functional teams in a growing biotech company.
The Senior Accountant will support the monthly close process, maintain financial records, and ensure scalable accounting processes while collaborating with the Accounting team on various reporting and compliance tasks.
The Senior Manager / Associate Director, HCP Marketing (US) will execute the HCP marketing strategy for Scholar Rock's first U.S. commercial launch of apitegromab, ensuring effective brand communication and integration.
The Director/Senior Director of Clinical Pharmacology will lead strategies in clinical pharmacology, utilizing modeling and simulation to guide the development of novel biologic therapies.
The Associate Director/Director of Patient Marketing will lead the non-personal promotion strategy for apitegromab, focusing on patient engagement and community presence in the SMA space.
The Regional Director, Rx Onboarding and Care Coordination, East leads and develops a team of coordinators to enhance patient support and access throughout the treatment journey for spinal muscular atrophy.
The Associate Director/Director of Clinical Operations Compliance will oversee adherence to standard procedures, support issue management, and ensure clinical programs are inspection ready.
The Senior Medical Science Liaison will engage with key opinion leaders and healthcare professionals, delivering scientific presentations and supporting clinical development in neuromuscular diseases.
The Vice President, Head of Regulatory Strategy will lead the Global Regulatory Strategy team, ensuring compliance and successful engagement with regulatory authorities across the portfolio.
The Sr. Medical Director, Drug Safety & Pharmacovigilance will lead safety strategy and risk management initiatives, ensuring compliance and effective evaluation of safety data for drug development projects.
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