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Executive Director/VP, Clinical Development

Zenas BioPharma is a global biopharmaceutical company committed to becoming a leader in the development and commercialization of immune-based therapies for patients around the world. With clinical development and operations globally, Zenas is advancing a deep and balanced global portfolio of potential first- and best-in-class autoimmune therapeutics in areas of high unmet medical need while meeting the value requirements of the dynamic global healthcare environment. The company’s pipeline continues to grow through our successful business development strategy. Our experienced leadership team and network of business partners drive operational excellence to deliver potentially transformative therapies to improve the lives of those living with autoimmune and rare diseases. 

We are seeking top talent who share our commitment to patients and have a track record of success in acquiring, developing and commercializing products across the globe. Our colleagues have an opportunity to engage in a fast-paced learning environment and experience individual and organizational success as we work towards becoming a global immunology and autoimmune disease leader, while living our values of Transparency, Relationships, Urgency, Excellence and Innovation – TRUE Innovation!

Position Summary:

The Executive Director/VP, Clinical Development is a highly visible role within the organization. In this strategic role, the individual will lead the clinical development plan for one or more assets within Zenas’ extensive portfolio and oversee the medical and safety responsibilities for global clinical trials across all phases of development. This individual will collaborate closely with Clinical Operations, Clinical Pharmacology, Medical and Scientific Affairs and other functions, and externally with Key Opinion Leaders and Investigators, Regulatory Authorities, Patient Advocacy Groups (PAG) and others involved in the scientific and clinical development process.

Key Responsibilities: 

  • Lead the clinical development plan and overall clinical strategy for multiple global programs.
  • Help to identify unmet medical needs in autoimmune disorders.
  • Overall responsibility for clinical study design, including:
    • authoring study synopses and protocols,
    • collaborating with biostats to develop the statistical analysis plan (SAP),
    • providing medical monitoring and safety oversight to ensure the safety of subjects and adherence to the protocol and good clinical procedures (GCP).
    • interpreting clinical data and authoring clinical study reports (CSR).
  • Develop strong relationships with Investigators, research sites and KOLs to design clinical trials that answer important medical questions.
  • Support publication strategy of clinical data through preparation and submission of clinical findings to scientific journals and conferences.
  • Lead clinical strategy for regulatory submissions, responses to regulatory questions and presentations at regulatory meetings.

Qualifications:

  • MD or MD/PhD in Rheumatology with 8 - 10 years of clinical development or equivalent experience, especially in late-stage clinical studies, preferred.
  • Clinical experience in Immunology, Rheumatology, or other autoimmune disorders a plus.
  • Demonstrated leadership, organization, and excellent written and verbal communication skills.
  • Ability to work collaboratively in a fast-paced, team-based matrix environment.
  • Experience leading global teams: experience working with China is highly valued.
  • Comfortable working in a demanding, fast-paced, start-up culture with evolving processes.

#LI-Hybrid

Zenas is committed to fair and equitable compensation practices. The base salary pay range for this role is $290,000 to $330,000 USD.. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location. 

Zenas believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Zenas’ competitive total rewards strategy that also includes annual performance bonus, equity, full range of benefits and other incentive compensation plans.

Zenas BioPharma is proud to be an equal opportunity employer. We are committed to fostering an environment where diversity is valued.  All qualified applicants will receive consideration for employment based on merit, qualifications and the needs of the business.

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EMPLOYMENT TYPE
Full-time, hybrid
DATE POSTED
November 24, 2024

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What You Should Know About Executive Director/VP, Clinical Development , Zenas BioPharma

At Zenas BioPharma, we are on a mission to transform lives through our innovative immunology and autoimmune disease therapies. We are currently looking for an experienced Executive Director/VP of Clinical Development to join our dynamic team in Waltham, MA. In this pivotal role, you'll not only shape the clinical development strategy for our extensive global programs, but also champion the safety and efficacy of groundbreaking therapies for autoimmune disorders. Your expertise will guide the design and oversight of clinical trials across all phases, ensuring our portfolio of first-in-class therapeutics meets the pressing medical needs of patients worldwide. Working closely with multidisciplinary teams, key opinion leaders, and regulatory authorities, your leadership will drive the successful completion of clinical studies and influence our publication strategy to share findings with the scientific community. At Zenas, we value Transparency, Relationships, Urgency, Excellence, and Innovation - TRUE Innovation! If you are a strategic thinker with a strong background in clinical development and a passion for improving patient lives, we invite you to help us revolutionize the healthcare landscape.

Frequently Asked Questions (FAQs) for Executive Director/VP, Clinical Development Role at Zenas BioPharma
What does the Executive Director/VP, Clinical Development role at Zenas BioPharma entail?

The Executive Director/VP, Clinical Development at Zenas BioPharma leads the clinical development strategy for various assets, guiding clinical trial designs and ensuring safety compliance while working collaboratively across departments and external partners.

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What qualifications are needed for the Executive Director/VP, Clinical Development position at Zenas BioPharma?

Candidates should possess an MD or MD/PhD in Rheumatology with 8-10 years of experience in clinical development, particularly in late-stage clinical studies, ideally with expertise in immunology and autoimmune disorders.

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How does the Executive Director/VP, Clinical Development contribute to Zenas BioPharma's mission?

The role is crucial as it shapes Zenas BioPharma's clinical strategy, ensuring that the development of innovative therapeutics is aligned with patient needs while driving operational excellence across trials.

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What kind of work environment can the Executive Director/VP, Clinical Development expect at Zenas BioPharma?

Expect a fast-paced and dynamic environment where collaboration is key, and your leadership will directly impact the development of potentially transformative therapies.

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What are the key responsibilities of the Executive Director/VP, Clinical Development at Zenas BioPharma?

Key responsibilities include leading global clinical development plans, defining study designs, overseeing medical safety for trials, and fostering relationships with KOLs while supporting regulatory submissions.

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What is the compensation range for the Executive Director/VP, Clinical Development at Zenas BioPharma?

The base salary range for this role is $290,000 to $330,000, with total rewards inclusive of bonuses, equity, and comprehensive benefits, reflecting Zenas's commitment to fair compensation.

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Is Zenas BioPharma an equal opportunity employer for the Executive Director/VP, Clinical Development role?

Yes, Zenas BioPharma prides itself on being an equal opportunity employer, promoting diversity and ensuring that all qualified applicants are considered based on merit and qualifications.

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Common Interview Questions for Executive Director/VP, Clinical Development
Can you explain your approach to leading a clinical development strategy?

When tackling clinical development strategies, I focus on aligning goals with patient needs, utilizing data to inform decisions, and fostering collaboration across teams to identify and address challenges effectively.

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Describe a challenging clinical trial you managed. What were the key learnings?

One notable challenge was navigating regulatory requirements in a multi-regional trial. Key learnings included the importance of proactive communication with regulatory bodies and how adaptability leads to better outcomes.

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How do you ensure safety oversight in clinical trials?

Safety oversight is paramount; I ensure robust monitoring by developing comprehensive risk management plans, conducting regular safety evaluations, and fostering an open environment for team collaboration on patient safety concerns.

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What key qualities do you believe are essential for success as an Executive Director in Clinical Development?

Essential qualities include strategic vision, strong communication skills, resilience in navigating challenges, and an unwavering commitment to patient-centric development practices.

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How do you approach collaboration with cross-functional teams?

Collaboration is built on transparent communication, mutual respect, and shared objectives. I prioritize regular meetings and create an inclusive atmosphere for input from team members at all levels.

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What strategies do you employ to identify unmet medical needs?

To pinpoint unmet medical needs, I leverage a combination of literature reviews, discussions with healthcare professionals, and feedback from patients to ensure our developments are addressing real-world gaps in treatment.

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How do you handle conflicts in a team setting?

In conflict situations, I promote open dialogue to understand differing perspectives, facilitate problem-solving sessions, and work towards consensus to maintain team cohesiveness and productivity.

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What experience do you have working with KOLs and research sites?

I have extensive experience nurturing relationships with KOLs and research sites by engaging in regular communications, aligning interests, and ensuring that the designed studies address critical research questions.

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In your opinion, what is the future of clinical development in biopharmaceuticals?

The future will be shaped by personalized medicine, technology integration such as AI in trial designs, and a strong emphasis on patient engagement throughout the clinical development process.

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How do you stay current with regulatory changes impacting clinical trials?

Staying updated requires continuous education through attending conferences, subscribing to key industry publications, and actively engaging with regulatory bodies to anticipate shifts that affect clinical trial processes.

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