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Sr. Associate Scientist, In Vivo Pharmacology

Why join us?

Parabilis Medicines is a highly distinctive young biopharmaceutical company whose intention is to grow over time into the ranks of major therapeutics companies.  Our foundational platform of Helicon™ therapeutics are peptides capable of efficient cell entry and modulation of both protein-protein and protein-DNA interactions. Through Helicon therapeutics, Parabilis is poised to revolutionize the medical possibilities for patients by precisely drugging intracellular targets long understood to be significant drivers of disease but never before drugged due to the limitations of existing drug modalities to act within the cell.

An important distinctive element of Parabilis is our lead program FOG-001, the company’s first-in-class TCF-blocking β-catenin inhibitor.  This compound is approximately 18 months and ~50 patients into our early development program for patients with advanced solid tumors, most importantly colorectal cancer. There are few products in the ecosystem with the medical and economic potential of FOG-001. Parabilis is fully leveraging the unprecedented potential Helicons present by deploying proprietary, custom-built machine learning and computational methods as part of its discovery and development process. Parabilis Medicines has raised more than $500 million to date from leading life sciences investors. Parabilis Medicines is headquartered in Cambridge, Mass.

What’s the opportunity?

The successful candidate will be part of our dedicated, dynamic thinking, and team-driven in vivo pharmacology group that is strongly engaged in the design and execution of pre-clinical activities to evaluate Helicon peptide therapeutics in oncology. It will require key hands-on technical execution and collaboration with external CROs to execute oncology preclinical studies. While acting as an individual contributor, this role has exciting opportunities to grow and develop as a drug hunter, as you will be a key cross-functional team member. As part of this growth, you will learn how to support pre-clinical expansion across oncology indications and communicate preclinical findings to senior leaders across the company. You will work within the existing pharmacology team framework and report directly to the AD of Pharmacology. Success in this role will require an industry understanding of pharmacology with a willingness to understand the scientific background in biology, the ability to manage multiple efforts in parallel, excellent communication skills, and an eagerness to grow as a drug hunter.

 

Key abilities of this role include

  • Execute in vivo studies to support a variety of research efforts, including target validation, therapeutic lead development, and Helicon platform advances
  • Support Parabilis in vivo pharmacology studies, both internally and externally
  • Participate in biological experiments (-omics, tissue culture, ex vivo) that support our in vivo initiatives
  • Perform in vivo PK/PD Efficacy studies to understand Helicon peptide on tumor growth inhibition, MOA, and metabolism
  • Act as a dynamic and collaborative in vivo team member who works closely with key stakeholders across our interdisciplinary research group
  • Identify and evaluate new in vivo models and technologies to enable novel genetic target validation and screening (transgenic, disease-relevant models, PDX)
  • Manage interactions with vendors and CROs
  • Prepare clearly articulated experimental reports and data presentations

What you’ll need to be successful:

  • BS with 5+ years of experience or MS with 3+ years of experience in the biotech or pharmaceutical industry
  • Expertise in human xenograft, PDX, mouse syngeneic, and mouse genetically engineered tumor models
  • Experience with multiple modes of drug delivery, including IP, IV, PO, and osmotic pump.
  • Experience with in vivo data analysis in support of preclinical and translational studies
  • Experience with minor and major surgical techniques, such as animal castration in oncology tumor models
  • Experience in drafting and implementing IACUC protocols
  • Experience in training and supervision of research associates in the design, execution, and data analysis of in vivo studies
  • The candidate must be self-motivated, able to lead and thrive in a team environment, and be comfortable working on and prioritizing multiple projects
  • Excellent written and oral communication skills
  • Able to work on-site and attend in-person meetings
  • Ready to undertake a “moonshot mission,” and work in a fast-paced, highly collaborative, and matrixed environment

Core Values

Parabilis Medicines is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit.

  • Creative. We are creating a whole new class of medicine requiring creativity to solve challenges as they arise, which we have successfully done since the inception of the company.
  • Patient-focused. We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.
  • Execution-oriented. As we begin clinical development and large-scale manufacturing, the team is balancing creativity and nimbleness with relentless, rigorous and flawless execution.
  • Humble. We fully appreciate that science and technology and policy are in flux, and we balance deep experience with humility to ask fundamental questions and seek newly available solutions.

As an equal opportunity employer, Parabilis Medicines values diversity and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

30 Acorn Park Drive    |     Cambridge, MA 02140    |    www.parabilismed.com

Average salary estimate

$100000 / YEARLY (est.)
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$80000K
$120000K

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What You Should Know About Sr. Associate Scientist, In Vivo Pharmacology, Parabilis Medicines

Join Parabilis Medicines as a Sr. Associate Scientist in In Vivo Pharmacology and be a part of a groundbreaking biopharmaceutical company in Cambridge, MA. At Parabilis, we are on a mission to redefine therapeutic landscapes through our innovative Helicon™ platform, which enables effective cell entry and modulation of protein interactions that have long been out of reach for traditional therapies. You will be a key player in our in vivo pharmacology group, driving preclinical research aimed at advancing our lead program, FOG-001—a revolutionary β-catenin inhibitor with immense potential for treating advanced solid tumors, including colorectal cancer. With approximately 50 patients already involved in our early development phase, the opportunities for impact are vast. In this role, you will design and execute in vivo studies, collaborate with external CROs, and engage in biological experiments while developing your skills as a drug hunter. From target validation to therapeutic lead development, you will manage and coordinate multiple projects amidst a dynamic team. Your input will be vital in communicating findings to senior leaders and shaping the future of our research endeavors. We’re looking for someone with a solid background in pharmacology, excellent communication skills, and a passion for teamwork. Parabilis offers an inspiring work environment committed to patient-focused innovation, where your creativity and execution-oriented mindset will thrive. Are you ready to embark on this exciting journey?

Frequently Asked Questions (FAQs) for Sr. Associate Scientist, In Vivo Pharmacology Role at Parabilis Medicines
What are the responsibilities of a Sr. Associate Scientist in In Vivo Pharmacology at Parabilis Medicines?

As a Sr. Associate Scientist in In Vivo Pharmacology at Parabilis Medicines, your primary responsibilities will include executing in vivo studies to support various research efforts related to Helicon peptide therapeutics. You'll collaborate closely with both internal teams and external CROs, contributing to the design and implementation of studies aimed at target validation and therapeutic lead development. You'll also engage in biological experiments, manage data analysis, and prepare detailed reports to present your findings to senior leadership.

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What qualifications are needed for the Sr. Associate Scientist, In Vivo Pharmacology position at Parabilis Medicines?

Candidates for the Sr. Associate Scientist, In Vivo Pharmacology position at Parabilis Medicines should possess a BS with at least 5 years or an MS with 3 years of experience in the biotech or pharmaceutical industry. Expertise in various tumor models including human xenografts and PDX, along with experience in drug delivery methods, IACUC protocol compliance, and surgical techniques for oncology models is essential. Strong communication skills and the ability to manage multiple projects are crucial for success in this role.

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What type of projects will I work on as a Sr. Associate Scientist at Parabilis Medicines?

In your role as a Sr. Associate Scientist in In Vivo Pharmacology at Parabilis Medicines, you will work on projects that focus on evaluating Helicon peptide therapeutics in oncology. This includes conducting target validation studies, assessing the pharmacokinetics and pharmacodynamics of new compounds, and developing novel in vivo models for validating genetic targets. Each project will require innovation and collaboration as you contribute to the broader goal of advancing potential therapies for cancer patients.

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How does the team dynamics work for the Sr. Associate Scientist at Parabilis Medicines?

At Parabilis Medicines, the team dynamics for the Sr. Associate Scientist role are characterized by a collaborative and interdisciplinary approach. You will work closely with cross-functional teams, including biology, chemistry, and clinical research, to drive your projects forward. Communication is key, and you'll be expected to present your findings to other team members and senior leadership. The supportive environment encourages sharing of ideas and fosters professional development.

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What is the career growth potential for a Sr. Associate Scientist in In Vivo Pharmacology at Parabilis Medicines?

The career growth potential for a Sr. Associate Scientist in In Vivo Pharmacology at Parabilis Medicines is significant. This role not only offers the chance to deepen your expertise in pharmacology but also provides pathways to take on more leadership responsibilities as you navigate and contribute to essential preclinical and translational research. By being actively involved in high-impact projects and collaborating with various departments, you’ll have opportunities to advance within the organization as you develop as a drug hunter.

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Common Interview Questions for Sr. Associate Scientist, In Vivo Pharmacology
Can you describe your experience with human xenograft and PDX models in oncology research?

When answering this question, provide specific examples of studies you've conducted using human xenograft or PDX models. Discuss the methodologies employed, the outcomes of these studies, and how they contributed to your understanding of tumor biology and treatment options. Highlight any relevant skills and techniques that you mastered, emphasizing your ability to apply these models to support preclinical research.

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How do you approach experimental design in in vivo studies?

In your response, explain your step-by-step process for designing in vivo experiments. Discuss how you define your objectives, select appropriate models, determine dosing regimens, and establish endpoints. Include how you ensure compliance with IACUC protocols and your strategies for analyzing data to draw meaningful conclusions from your experiments.

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What strategies do you use to manage multiple ongoing projects effectively?

To manage multiple projects, I prioritize tasks based on urgency and impact, ensuring that I allocate sufficient resources and time to each effort. I use project management tools to track progress and communicate with team members about deadlines and responsibilities. Keeping open lines of communication with my team members is crucial, as it allows for flexibility in shifting priorities when necessary and ensures we stay aligned with our goals.

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Can you provide an example of a challenging problem you faced in an in vivo study and how you resolved it?

Think of a specific instance involving a setback in an in vivo study. Describe the nature of the challenge, the steps you took to analyze the situation, and any innovative solutions you implemented. Highlight your ability to remain focused and proactive, showcasing your problem-solving skills and resilience as a researcher.

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How do you keep up-to-date with the latest developments in pharmacology and oncology?

Convey your commitment to continuous learning by mentioning the journals, conferences, and online platforms you regularly follow. Discuss any professional networks or associations you’re part of which help you stay informed about recent breakthroughs and emerging technologies in pharmacology and oncology, and how this knowledge influences your research.

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What collaboration experiences have you had with external CROs, and what did you learn?

Share insights about your previous collaborations with CROs by detailing specific projects, your role, and the outcomes. Discuss the lessons learned, including best practices for communication, project management, and setting expectations. Emphasize any skills you gained in navigating these relationships and how they have shaped your approach to teamwork in a research setting.

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How do you ensure that your in vivo studies are conducted in compliance with relevant regulations?

I prioritize compliance by staying well-versed in IACUC guidelines and other relevant regulations before initiating any study. This includes thorough planning, preparation of the necessary protocols, and obtaining all required approvals. Regular training sessions and review of compliance standards with my team help reinforce these practices, ensuring our studies are conducted ethically and responsibly.

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What do you think is the most exciting aspect of working in in vivo pharmacology?

The most exciting aspect of my work in in vivo pharmacology is the opportunity to make a tangible difference in patients' lives by contributing to the discovery of novel therapeutics. Being at the forefront of translating innovative scientific ideas into real-world treatments compels me. I enjoy the challenge of finding solutions to complex biological questions and the thrill of collaboration with diverse teams to drive research forward.

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Describe your experience in training and mentoring junior staff in research techniques.

When asked this question, provide specific examples of how you have trained or mentored junior researchers or interns in your previous roles. Discuss the techniques you taught, how you customized your approach based on their skill levels, and the outcomes of your mentorship. Emphasize your belief in the importance of knowledge transfer in scientific research.

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How do you communicate complex scientific findings to a non-scientific audience?

To communicate complex findings effectively, I focus on simplifying the key concepts and using analogies or relatable terms. Visual aids such as graphs, infographics, or charts can also help convey the message clearer. Practice in this area allows me to tailor my explanations according to the audience's expertise, ensuring that they grasp the essential points without overwhelming them with technical jargon.

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EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
December 9, 2024

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