Director / Sr. Director, Clinical Operations - Oncology
- Scholar Rock Inc.
- Full time
- Cambridge, Massachusetts
- Posted: February 18, 2023
Company
Scholar Rock is a Phase 3, 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 selective inhibitor of the activation of the growth factor myostatin in skeletal muscle, is in development for the treatment of spinal muscular atrophy, or SMA. Following positive results from the TOPAZ Phase 2 trial in patients with Type 2 and Type 3 SMA, we are now advancing apitegromab development through SAPPHIRE, an ongoing, randomized, double-blind, placebo-controlled, phase 3 clinical trial. In addition, we are conducting our DRAGON Phase 1 proof-of-concept trial for SRK-181, a selective inhibitor of latent TGFβ1 activation, in patients with locally advanced and metastatic solid tumors.
By combining our deep structural insights with antibody drug discovery, Scholar Rock is creating a pipeline of novel product candidates with the potential to transform the lives of patients suffering from a wide range of serious diseases, including neuromuscular disorders, cancer, and fibrosis.
Summary of Position:
Scholar Rock is looking for a director-level subject matter expert to build and lead a clinical operations team focused on advancing our immuno-oncology clinical programs while upholding our core values and staying true to our mission. Reporting to the Head of Clinical Operations, the Director, Clinical Operations will play a key role in the operational planning, oversight, and delivery for one or more clinical programs.
Position Responsibilities
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- Develop and implement clinical project plans in accordance with corporate objectives
- Evaluate outsourcing partnerships and define go-forward strategy for identifying, engaging and managing long term strategic partnerships
- Provide oversight of clinical operation activities (trial management, site monitoring, vendor management, TMF, data operations, IMP management, etc.) for one or more clinical trials.
- Contribute to key study documents in conjunction with other functional area leads (e.g. protocols, project plans and timelines, statistical analysis plans, final study reports, etc.)
- Proactively develop and implement hiring plans to attract, recruit, on-board and retain best in class talent to effectively execute against program milestones
- Ensure clinical trial compliance with all SOPs and GCP/ICH guidelines; maintain an inspection readiness state throughout the lifecycle of the trial
- Proactively identify, resolve and escalate issues that jeopardize clinical study completion on time or within budget
- Identify, evaluate, and recruit clinical trial sites
- Contribute to global clinical / regulatory submissions
- As a subject matter expert, actively educate, engage with and seek input from key stakeholders to bolster organizational effectiveness and efficiency
- Undertake line management responsibilities for assigned team members, serving as coach and mentor
- Contribute to the development of departmental SOPs and work instructions
- May require travel, including international travel
Candidate Requirements:
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- Bachelor’s in a scientific discipline; advanced degree preferred
- Minimum 10 years of experience in a biotech/pharmaceutical/ CRO setting, principally in oncology drug development; minimum 7 years of clinical operations experience; minimum 5 years in a supervisory role
- Proven record of success running oncology/ immuno-oncology 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
Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.