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Senior Director, Clinical Development

Jasper is a clinical-stage biotechnology company developing briquilimab, a novel antibody targeting c-Kit (CD117) as a therapeutic for chronic mast and stem cell diseases. Jasper is currently conducting clinical studies of briquilimab as a treatment in patients with CSU or with CIndU and is initiating a clinical study in patients with asthma. Briquilimab is also currently in clinical studies as a treatment for patients with LR-MDS and as a conditioning agent for cell therapies for rare diseases. To date, briquilimab has a demonstrated efficacy and safety profile in more than 160 dosed participants and healthy volunteers, with clinical outcomes in CIndU, and as a conditioning agent in severe combined immunodeficiency (SCID), acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), Fanconi anemia (FA), and sickle cell disease (SCD).


Summary
  • Reporting to the SVP of Clinical Development, the Senior Medical Director leads the direction, planning, execution, and interpretation of clinical trials of one or more Phase 1 through 3 clinical development programs at Jasper, focused on advancing Briquilimab and other novel stem and mast cell targets and molecules. Participates in and leads cross-functional teams to generate, deliver, and disseminate high-quality clinical data supporting overall product scientific and business strategy. 


Responsibilities
  • Build strategic and coordinated clinical development plans which are aligned with business objectives and overall corporate strategy. 
  • Leads and demonstrates ownership of the design and implementation of multiple clinical development protocols of the overall product development plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, markets, business operations, and emerging issues. Oversees project-related education of investigators, study site personnel, and Jasper study staff. 
  • Leads the Clinical Sub team (CST, a cross-functional matrix team, reporting to the Program Team; is seen as the clinical designee to the PT, driving team alignment and decision making across functions and ensuring smooth communication between the PT and the Global Franchise Committee (GFC) as well as the Clinical Development line function.  
  • Has overall responsibility for leading clinical study teams, monitoring overall study integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is responsible for ensuring agreed-upon study enrollment and overall timelines for key deliverables.  
  • Primary responsibility for and ownership of design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other program documents. 
  • Work collaboratively with Medical and/or Scientific Directors and Clinical Scientists working on the same or related programs. 
  • Serves as an in-house clinical expert for one or more molecules and diseases in the therapeutic area, coordinating and leading appropriate scientific and medical activities with internal stakeholders as they relate to ongoing projects.  
  • May participate in or lead clinical development contributions to due diligence or other business development activity. As required by program needs, contributes in partnership with Research colleagues to design and implementation of translational strategies. 
  • Acts as clinical lead and actively solicits opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are incorporated into Clinical Development Plans and protocols as appropriate. 
  • Stays informed of professional information and technology through conferences, medical literature, and other available training, to augment expertise in the therapeutic area. May represent Jasper at key external meetings. 
  • Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as a clinical representative for key regulatory discussions. 


Requirements
  • Medical Doctor (M.D.) or non-US equivalent of M.D. degree, PhD or PharmD required.   
  • At least 5-10 years of experience in the pharmaceutic or biotech industry required, experience in small to midsize biotech preferred.  
  • Proven track record of leadership in clinical trial design and execution including both early (Phase 1) and later stage (Phase 2 and 3) development experience in the biotech or pharmaceutical industry required.  
  • Proven leadership skills to lead a global cross functional team   
  • Clinical and/or development experience in immunology, respiratory, or allergy preferred.  
  • Experience with filing original NDA or BLA required with additional sNDA or sBLA experience a plus. 
  • Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in development of clinical strategy and the design of study protocols. 
  • Must thrive working in a fast-paced innovative environment while remaining flexible, proactive, resourceful, and efficient. 
  • Demonstrated ability to translate strategy into action. Excellent analytical skills, ability to communicate complex issues in a simple way, and ability to orchestrate plans to resolve issues and mitigate risks. 
  • Outstanding organizational and interpersonal skills, and outstanding ability to manage relationships and influence others. 
  • Willingness to be both a strategic leader and hands-on problem solver. 


$240,000 - $300,000 a year

We offer our employees comprehensive benefits.


Jasper is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by applicable law.

 

Company Values:

·       Respect

·       Collaboration

·       Integrity

·       Responsible

·       Excellence

·       Acknowledgment

 

Mission:

Our mission is to make safer and potentially curative therapy possible for more patients in need. We are bringing together a team of high performing biotech professionals, leading academic institutions and a strong syndicate of healthcare-focused investors to achieve our vision 

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Average salary estimate

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$240000K
$300000K

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What You Should Know About Senior Director, Clinical Development, Jasper Therapeutics

Are you ready to take your career to the next level as a Senior Director of Clinical Development at Jasper? This innovative biotechnology company, located in Redwood City, CA, is on the cutting edge of developing briquilimab, a novel antibody targeting c-Kit for chronic mast and stem cell diseases. In this pivotal role, you'll report to the SVP of Clinical Development and lead the direction, planning, and execution of clinical trials from Phase 1 to 3. Your expertise will guide multi-disciplinary teams to generate high-quality clinical data that supports Jasper's scientific and business objectives. You'll design and oversee the implementation of clinical development protocols, ensuring compliance with regulatory requirements while guiding cross-functional teams. Your responsibilities will include educating study personnel, monitoring study integrity, and analyzing results related to briquilimab and other innovative treatments. As a clinical expert, your insights will influence various teams, contributing to vital projects while representing Jasper in key external meetings. If you thrive in a fast-paced environment and possess strong leadership skills, this is an exciting opportunity to make a significant impact in the biotech world. Join Jasper on our mission to create safer and potentially curative therapies for patients in need!

Frequently Asked Questions (FAQs) for Senior Director, Clinical Development Role at Jasper Therapeutics
What are the responsibilities of the Senior Director of Clinical Development at Jasper?

The Senior Director of Clinical Development at Jasper is responsible for leading the planning, execution, and analysis of clinical trials ranging from Phase 1 to 3. This includes the design of clinical development protocols, management of cross-functional teams, and ensuring compliance with regulatory standards while aligning clinical strategy with the company's business objectives.

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What qualifications are required for the Senior Director of Clinical Development position at Jasper?

Candidates for the Senior Director of Clinical Development role at Jasper must have an M.D. or equivalent, with 5-10 years of experience in the pharmaceutical or biotech industry, particularly in clinical trial design and execution. Leadership skills in managing global teams and familiarity with regulatory requirements are also essential.

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What type of experience is preferred for the Senior Director of Clinical Development role at Jasper?

Jasper prefers candidates with a background in immunology, respiratory, or allergy clinical development, along with a proven track record in both early (Phase 1) and later-stage (Phase 2 and 3) clinical trials. Experience in filing original NDAs or BLAs is crucial for this position.

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How does the Senior Director of Clinical Development at Jasper interact with other teams?

The Senior Director of Clinical Development at Jasper collaborates closely with Medical Affairs, Commercial teams, and other cross-functional units to integrate various perspectives into clinical development plans. This role involves significant leadership in team meetings to ensure alignment and communication across functions.

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What is the salary range for the Senior Director of Clinical Development position at Jasper?

The compensation for the Senior Director of Clinical Development position at Jasper ranges from $240,000 to $300,000 annually, reflecting both the significant responsibilities of the role and the extensive expertise required.

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Common Interview Questions for Senior Director, Clinical Development
Can you describe your experience in leading clinical trials, particularly in the biotech industry?

When answering this question, highlight specific trials you have led, detailing your role, the therapeutic area you focused on, and the outcomes achieved. Use examples to illustrate your leadership style and the collaboration with cross-functional teams.

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What strategies do you employ to ensure compliance with regulatory requirements during clinical trials?

Discuss your approach to staying informed about the latest regulations and compliance guidelines. Provide examples of how you have implemented training or systems to ensure all team members adhere to these standards during trial design and execution.

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How do you approach the design of clinical development protocols?

Discuss your methodology for integrating scientific principles with regulatory requirements. Share past examples of protocols you've designed, emphasizing your thought process in addressing safety, efficacy, and business strategy.

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Can you give an example of a challenging clinical project and how you overcame obstacles?

When providing an example, be specific about the challenges faced and detail the strategies you employed to navigate them. Highlight your problem-solving skills and the impact of your decisions on the project’s success.

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How do you manage relationships with key opinion leaders in the therapeutic area?

Explain your approach to building and maintaining relationships with KOLs, including how you engage with them for insights, guidance, and feedback. Include specific strategies you use for collaboration and communication.

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What techniques do you use to monitor the safety and efficacy of trial data?

Share your preferred methods for data analysis, including statistical tools or practices you follow. Discuss how you ensure safety monitoring aligns with industry standards and contributes to informed decision-making.

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In your opinion, what makes a successful clinical study?

Provide your insights on the characteristics of successful clinical studies, such as clear design, effective communication, thoughtful team dynamics, and rigorous adherence to timelines. Relate these points to your past experiences.

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How do you stay updated on advancements in your therapeutic area?

Discuss your commitment to continuous education through professional conferences, medical literature, and training. Mention specific resources or networks you leverage to stay informed about industry trends and developments.

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What is your experience with filing NDAs or BLAs?

Share specific experiences related to NDA or BLA submissions, detailing your role in the process, the challenges encountered, and the outcomes achieved. Highlight your understanding of regulatory expectations.

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How do you handle conflicts within a cross-functional team?

Outline your approach towards conflict resolution, emphasizing open communication, active listening, and collaboration. Provide a specific example of a past experience where you effectively managed a conflict to reach a productive outcome.

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Full-time, on-site
DATE POSTED
March 22, 2025

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