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Clinical Program Lead

Company Overview
TwoStep Therapeutics is at the forefront of innovation in cancer treatment, pioneering a multi-targeting platform aimed at advancing a pipeline of targeted therapies applicable to a wide range of solid tumors. Our mission is to transform cancer care by extending precision medicine to diverse tumor types and patient populations, particularly those with limited options. Founded by industry leaders including CEO Caitlyn Miller, Stanford Professors Jennifer Cochran, Ronald Levy, and Nobel Laureate Carolyn Bertozzi, TwoStep Therapeutics emerged from Stanford in March 2024 and is backed by NFX and other prominent biotech investors.

 

Position Overview
We are seeking a dynamic Clinical Program Lead to spearhead the delivery of our tumor-targeted therapies to patients. In this pivotal role, you will be responsible for the design and implementation of clinical stage programs, making this an exciting opportunity for a driven drug developer eager to influence the future of cancer treatment and enhance patient outcomes.

 

Key Responsibilities

  • Lead clinical development activities within a cross-functional team, from early to late-phase clinical studies.

  • Develop comprehensive clinical development plans and study designs, including the creation of study concepts, protocols, and essential regulatory documentation.

  • Conduct medical monitoring and ensure timely execution of clinical trials.

  • Establish and maintain relationships with Key Opinion Leaders (KOLs) and act as the primary clinical representative in all regulatory and external communications.

 

Essential Qualifications

  • Master’s degree or equivalent in a related field, or a combination of education and relevant experience.

  • 5+ years of experience in clinical development with a PhD or MD; 8+ years with a Master’s; 10+ years with a Bachelor’s degree.

  • Extensive experience in both early and late-phase clinical development.

  • Proficiency in authoring regulatory documents and a strong understanding of the drug development process.

  • Solid grasp of clinical research methodologies and biostatistics principles.

  • Comprehensive knowledge of FDA, EMA, MHRA, and ICH GCP guidelines.

  • Exceptional attention to detail, a commitment to high-quality work, and a strong sense of urgency to achieve team objectives.

  • Proven leadership in managing complex projects and a track record of delivering results.

  • Excellent verbal and written communication skills.

  • Strong analytical, problem-solving, and strategic planning abilities.

Preferred Qualifications

  • Experience in clinical oncology drug development, particularly with tumor-targeted drug conjugates (e.g., peptide-drug conjugates, antibody-drug conjugates, etc.), immunotherapy, or radioligand therapy.

 

What We Offer
At TwoStep Therapeutics, we envision a future where every cancer patient has access to targeted, safe, and effective therapeutic options. We prioritize a diverse, inclusive work environment that fosters personal and professional growth. Our comprehensive benefits include:

  • Competitive base salary and equity compensation

  • Unlimited Paid Time Off (PTO)

  • Comprehensive medical, dental, and vision benefits for individuals and families

  • 401(k) plan

  • Company-paid basic life insurance

 

Job title and compensation are dependent on the candidate’s experience and skillset.

 

Equal Opportunity Employer
TwoStep Therapeutics is an equal opportunity employer. We prohibit unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law. If you require assistance in submitting an application due to incompatible assistive technology or a disability, please contact us at hiring@twosteptx.com. We are committed to accommodating your needs promptly.

 

Join Us
If you are passionate about advancing cancer therapies and want to make a meaningful impact in the field, we invite you to apply for the Clinical Program Lead position at TwoStep Therapeutics. Together, we can shape the future of cancer treatment.

Average salary estimate

$150000 / YEARLY (est.)
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$120000K
$180000K

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What You Should Know About Clinical Program Lead, TwoStep Therapeutics

Are you ready to make a transformative impact in the world of cancer treatment? Join us at TwoStep Therapeutics as a Clinical Program Lead! Based in San Carlos, we are on a mission to revolutionize cancer care with our pioneering multi-targeting platform aimed at developing effective therapies for a variety of solid tumors. As our Clinical Program Lead, you'll be at the forefront of this innovation, playing a vital role in designing and implementing clinical stage programs that can change lives. You'll lead an energetic, cross-functional team through the intricacies of early to late-phase clinical studies, ensuring that our tumor-targeted therapies reach patients who need them most. Your expertise will guide the creation of comprehensive clinical development plans, protocols, and crucial regulatory documents. Building relationships with Key Opinion Leaders and representing our clinical interests externally will also be key aspects of your role. If you have at least 5 years of clinical development experience, preferably with a PhD or MD, and are set to make a lasting impact in oncology, we would love to hear from you. At TwoStep Therapeutics, we celebrate diversity and creativity, offering competitive salaries, unlimited PTO, comprehensive benefits, and a collaborative work environment. Let's shape the future of cancer treatment together!

Frequently Asked Questions (FAQs) for Clinical Program Lead Role at TwoStep Therapeutics
What are the responsibilities of a Clinical Program Lead at TwoStep Therapeutics?

The Clinical Program Lead at TwoStep Therapeutics is responsible for leading clinical development activities within a diverse team, spanning both early and late-phase clinical studies. This includes crafting and executing clinical development plans, study protocols, and regulatory documentation, as well as managing medical monitoring to ensure timely trial execution.

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What qualifications are needed for the Clinical Program Lead role at TwoStep Therapeutics?

To qualify for the Clinical Program Lead position at TwoStep Therapeutics, candidates should possess a Master's degree or higher in a relevant field and have a minimum of 5 years of experience in clinical development. A deep understanding of the drug development process and regulatory requirements is essential.

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How does the Clinical Program Lead contribute to patient outcomes at TwoStep Therapeutics?

The Clinical Program Lead plays a crucial role in ensuring that tumor-targeted therapies are thoughtfully developed and executed. By guiding clinical trials and fostering essential collaborations with Key Opinion Leaders, this role directly impacts the effectiveness and accessibility of cancer treatments for patients in need.

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What kind of team environment can a Clinical Program Lead expect at TwoStep Therapeutics?

At TwoStep Therapeutics, the Clinical Program Lead will work within a dynamic and collaborative team environment. The company emphasizes a culture of diversity and inclusivity, encouraging creative thinking and professional growth among team members focused on advancing cancer therapies.

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What benefits does TwoStep Therapeutics offer to its Clinical Program Lead?

TwoStep Therapeutics provides a comprehensive benefits package that includes a competitive salary, equity compensation, unlimited Paid Time Off, health benefits for individuals and families, and a 401(k) plan. The company is committed to fostering a supportive work environment where employees can thrive both personally and professionally.

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Common Interview Questions for Clinical Program Lead
Can you describe your experience with clinical development?

When answering this question, focus on specific projects you've led, highlighting your role in developing study plans and protocols. Discuss any challenges you've faced and how you've navigated regulatory hurdles to ensure successful clinical trials.

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How do you ensure effective communication with cross-functional teams?

Share examples of how you've facilitated communication in past roles, perhaps through regular meetings, updates, or using collaboration tools. Highlight your interpersonal skills and ability to foster collaborative relationships across departments.

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What strategies do you use for developing regulatory documents?

Talk about your methodical approach to crafting regulatory documents, emphasizing your attention to detail and compliance with FDA, EMA, and ICH GCP guidelines. Provide examples of documents you've authored and how they contributed to successful clinical trials.

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How do you prioritize tasks when managing multiple projects?

Outline your approach to prioritization, whether through time management tools, project management software, or team input. Highlight the importance of aligning project goals with overall company objectives to maintain strategic focus.

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What is your experience with tumor-targeted therapies?

Discuss your relevant experience with tumor-targeted therapies, including any specific drug development projects. Emphasize your understanding of the intricacies involved in developing such therapies and your commitment to innovative approaches.

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How do you keep updated on industry developments?

Share your methods for staying informed, such as attending conferences, joining professional organizations, or following relevant publications. Demonstrating a proactive stance on continued learning will showcase your dedication to the field.

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Can you describe a challenging clinical trial you managed?

Use the STAR method (Situation, Task, Action, Result) to describe a specific example, focusing on the challenges faced, actions taken to address them, and the successful outcome. This will highlight your problem-solving and leadership skills.

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What role do Key Opinion Leaders play in clinical trials, and how do you engage with them?

Explain the significance of KOLs in providing insights and validating study designs. Share your strategies for building relationships with KOLs, such as regular communication, collaboration on research initiatives, and inviting them to participate in advisory boards.

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How do you approach analytical problem-solving in clinical development?

Discuss your method for assessing data, identifying trends, and applying analytical reasoning to inform decisions in clinical development. Offering specific examples of how your analytical skills have driven project success will strengthen your response.

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What motivates you to lead in the field of clinical oncology?

Express your passion for cancer research and improving patient outcomes, sharing any personal anecdotes that might have influenced your career choice. Highlight your commitment to teamwork and leading with empathy to foster a positive work environment.

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DATE POSTED
December 6, 2024

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