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Associate Director, Clinical Sciences

Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role.

 

Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at ScholarRock.com and follow @ScholarRock and on LinkedIn.


Summary of Position:


The Associate Director, Clinical Sciences is a key position in our Clinical Development Group that will help drive the next phase of Scholar Rock’s growth with energy and dedication. This candidate will drive strategy and decision-making in collaboration with other functions by ensuring relevant information, analysis, and expertise are considered. This position requires a highly organized, collaborative, and adept clinical scientist with strong critical thinking skills, attention to detail, and agility. The current position is focused on the investigational agent apitegromab and its development for Spinal Muscular Atrophy (SMA) as well as other neuromuscular indications, including supportive activities and study oversight. Responsibilities may encompass clinical programs in phases 1 through 4. 


Position Responsibilities
  • Provide cross-functional clinical sciences support to internal stakeholders for portfolio decision-making and clinical development strategy/planning. This may include review and synthesis of scientific literature, clinical & competitive landscape analysis, and summaries of clinical development innovations.
  • Ensure currency with innovative development strategy and competitive approach in key disease areas of interest.
  • Provide strategic scientific expertise to develop and oversee all aspects of clinical projects including design, start-up, execution, analysis, and reporting of clinical studies.
  • Anticipate opportunities or challenges well in advance; can effectively gather insight from internal stakeholders and external consultants for depth of the issue and perspective.
  • Ensure strong representation of clinical sciences team at key governance bodies and teams (e.g., PRC, early program teams).  Articulately convey key considerations to an issue and creative ideas or solutions for leaders to consider. 
  • Provide scientific and content support on a broad set of activities, including study advisory boards, development leadership meetings, board presentations, and R&D Day presentations.
  • Foster and maintain relationships with key external advisors and partners.
  • Ensure highly organized and accessible content management: e.g., literature related to new indications, innovative trial designs, relevant scientific data.
  • Provide clinical sciences support to clinical stage programs, including manual data review and authoring or reviewing study related documents (study concepts, clinical protocols and amendments, investigator brochures, statistical analysis plans, clinical study reports, and safety updates).  
  • Provide development support for business development activities.


Candidate Requirements
  • Advanced degree in Life Sciences (MD, PhD, Pharm D, or MS) strongly preferred
  • Therapeutic expertise: Neuromuscular disease strongly preferred
  • 3+ years of experience in biopharmaceutical industry in clinical development or clinical science with a proven track record of driving for results
  • Strong critical thinking skills, including ability to synthesize large body of information and make decisions based on robust available information
  • Experience with clinical study design, clinical data interpretation and publications, and working knowledge of biostatistics and pharmacology
  • Experience to build strong relationships with both internal stakeholders and external scientific and medical community
  • Highly organized, results-oriented, with excellent interpersonal and communication skills, including ability to integrate diverse perspectives to drive timely decision-making
  • Exceptional communication skills & extensive experience and excellent skills in developing PowerPoint presentations
  • Ability to travel domestically and internationally (~10%). 


Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees

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Average salary estimate

$140000 / YEARLY (est.)
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$120000K
$160000K

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What You Should Know About Associate Director, Clinical Sciences, Scholar Rock

As the Associate Director of Clinical Sciences at Scholar Rock, you will be a driving force in our mission to develop transformative therapies for serious diseases. Working remotely, your role is integral to our Clinical Development Group, where your expertise will contribute to the advancement of innovative treatments, with a specific focus on apitegromab for Spinal Muscular Atrophy (SMA) and additional neuromuscular conditions. At Scholar Rock, we are proud to lead the way in utilizing the biology of the transforming growth factor beta (TGFβ) superfamily, with a commitment to addressing high unmet medical needs through cutting-edge science. Your responsibilities will involve collaborating with cross-functional teams, synthesizing critical data, and designing robust clinical studies. With your strong critical thinking skills and attention to detail, you'll anticipate challenges and identify opportunities ahead of time, helping shape our clinical strategies. The ideal candidate will have a deep understanding of clinical study design and the ability to foster relationships with external advisors, making a real impact in the biotech field. If you're passionate about improving patient outcomes and want to help us unlock new possibilities in treatment options, Scholar Rock eagerly awaits your input and leadership.

Frequently Asked Questions (FAQs) for Associate Director, Clinical Sciences Role at Scholar Rock
What does an Associate Director of Clinical Sciences do at Scholar Rock?

The Associate Director of Clinical Sciences at Scholar Rock plays a crucial role in driving the strategic development of innovative clinical programs. This involves collaborating with various teams, analyzing clinical data, and overseeing the progression of clinical studies from design to implementation.

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What qualifications are needed for the Associate Director, Clinical Sciences position at Scholar Rock?

Candidates looking to apply for the Associate Director, Clinical Sciences position at Scholar Rock should ideally hold an advanced degree in Life Sciences, have experience in clinical development and data interpretation, and possess strong organizational and critical thinking skills.

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What are the responsibilities of the Associate Director in Clinical Sciences at Scholar Rock?

The responsibilities of the Associate Director in Clinical Sciences at Scholar Rock include supporting clinical development strategies, overseeing clinical project execution, engaging in competitive landscape analysis, and maintaining strong relationships with external advisors, along with managing clinical documentation.

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What is Scholar Rock's focus in the biopharmaceutical industry?

Scholar Rock focuses on developing life-changing therapies through the modulation of growth factors, particularly targeting serious diseases like neuromuscular disorders and conditions such as spinal muscular atrophy. This innovative approach places the company at the forefront of scientific advancements in therapeutic development.

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What experience is typically required for the Associate Director role at Scholar Rock?

Typically, the Associate Director role at Scholar Rock requires candidates to have over three years of experience in the biopharmaceutical industry within clinical development, showcasing a proven history of driving results in complex clinical settings.

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How does Scholar Rock prioritize team collaboration in the role of Associate Director?

In the role of Associate Director, Scholar Rock prioritizes collaboration across various functional teams. This includes fostering open communication to include diverse perspectives, ensuring that all insights and innovations are leveraged to drive forward clinical developments effectively.

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Is remote work available for the Associate Director, Clinical Sciences position at Scholar Rock?

Yes, the Associate Director, Clinical Sciences position at Scholar Rock is a remote role, allowing candidates the flexibility to work from anywhere while still contributing significantly to impactful clinical advancements.

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Common Interview Questions for Associate Director, Clinical Sciences
Can you describe a successful clinical trial you managed in your previous role?

When discussing a successful clinical trial you managed, focus on your specific role in the process, the challenges you overcame, how you collaborated with other teams, and the outcomes achieved. Highlight data-driven results and any significant learnings from the experience.

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How do you ensure compliance and quality in clinical studies?

To ensure compliance and quality in clinical studies, emphasize your familiarity with regulatory standards, your routine checks for adherence protocols, and how you train, guide, and motivate your team on best practices to maintain quality throughout study phases.

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What strategies do you employ to resolve conflicts in a clinical research setting?

Discuss your proactive approach and communication skills in resolving conflicts, such as setting up meetings for open dialogue, actively listening to concerns, and seeking collaborative solutions that keep the focus on the project's success.

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Describe how you stay updated on trends within the neuromuscular disease field.

Indicate your commitment to continuous learning through attending conferences, reading scientific journals, participating in relevant webinars, and networking with industry experts. Show your passion for applying the latest findings to enhance clinical strategies.

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How do you approach data analysis and interpretation during clinical trials?

Share your techniques for analyzing clinical data, such as leveraging statistical tools, collaborating with biostatisticians, and interpreting results in the context of existing literature. Discuss how you communicate this data to stakeholders effectively.

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What role do you believe cross-functional collaboration plays in clinical development?

Highlight the essential nature of cross-functional collaboration in clinical development, as it ensures various expertise is integrated into the process. Explain how diverse perspectives enhance decision-making and ultimately lead to successful clinical outcomes.

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Can you provide an example of how you’ve improved a clinical study process?

When providing an example of improvement in a clinical study process, focus on a specific initiative you led, the methods you implemented to enhance efficiency, and quantify the impact it had on timelines, costs, or data quality.

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How would you handle a situation where a clinical trial is falling behind schedule?

In handling delays in a clinical trial, emphasize your problem-solving skills. Discuss your approach to identifying root causes, re-evaluating timelines, communicating transparently with the team, and reallocating resources or adjusting processes wherever feasible.

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What is your experience in developing clinical study protocols?

Share your extensive experience in developing clinical study protocols, detailing your involvement from concept to execution. Discuss how you ensure protocols meet regulatory standards and the engagement of all necessary stakeholders.

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Why do you want to work at Scholar Rock as the Associate Director?

Express your enthusiasm for Scholar Rock’s innovative approach to biopharmaceuticals and its commitment to addressing high unmet needs in healthcare. Align your professional values and career goals with the company’s mission and vision, demonstrating your fit for the role.

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Full-time, remote
DATE POSTED
November 23, 2024

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