Senior Director - Clinical Operations

4 days ago

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Scholar Rock

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Scholar Rock is a clinical-stage biopharmaceutical company focused on the discovery and development of innovative medicines for the treatment of serious diseases in which signaling by protein growth factors plays a fundamental role. Our most advanced investigational product candidate, apitegromab (SRK-015), a

51 - 200 employees

Founded 2016

💰 $205M Post-IPO Equity on 2022-06

📋 Description

• Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases. • Global leader in the biology of the transforming growth factor beta (TGFβ) superfamily. • Focused on advancing innovative treatments where protein growth factors are fundamental. • Created a pipeline for neuromuscular disease, cardiometabolic disorders, and cancer. • Only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). • Commitment to unlocking fundamentally different therapeutic approaches powered by proprietary platform. • Develop novel monoclonal antibodies to modulate protein growth factors. • Harnessing cutting-edge science in historically under-addressed disease spaces. • Creating new possibilities for patients.

🎯 Requirements

• Bachelor’s Degree (scientific discipline preferred); advanced degree preferred • Minimum 12 years of experience in a biotech/pharmaceutical/ CRO setting; minimum 10 years of clinical operations experience; minimum 5 years in a supervisory role • Proven record of success running complex drug development trials • Demonstration of effective leadership through vision for her/his team, coaching and mentoring, and organizational development • Highly organized, outcome oriented, self-motivated performance • Comfortable in a fast-paced environment with the ability to adapt to change • In depth knowledge and understanding of all aspects of clinical operations management, with a track record of successfully managing programs to completion on time and on budget • Excellent interpersonal skills, ability to develop important relationships with key stakeholders across a variety of disciplines, good conflict management and negotiation skills • Ability to analyze complex issues to develop relevant and realistic plans, programs and recommendations • Excellent working knowledge of federal regulatory requirements and guidelines for Good Clinical Practice • Outstanding oral and written communication skills including experience authoring clinical protocols and other key trial documents

🏖️ Benefits

• Equal Opportunity Employer. • Celebrate diversity. • Commitment to an inclusive environment.