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Senior Scientist

Company Summary: Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform. Korro is generating a portfolio of differentiated programs that are designed to harness the body’s natural RNA editing process to effect a precise yet transient single base edit. By editing RNA instead of DNA, Korro is expanding the reach of genetic medicines by delivering additional precision and tunability, which has the potential for increased specificity and improved long-term tolerability. Using an oligonucleotide-based approach, Korro expects to bring its medicines to patients by leveraging its proprietary platform with precedented delivery modalities, manufacturing know-how, and established regulatory pathways of approved oligonucleotide drugs. Korro’s lead program is Alpha-1 Antitrypsin Deficiency (AATD). Korro is based in Cambridge, Massachusetts.


We are collaborative and united by a common mission. We are building a company with extraordinary people with an audacious vision to create transformative genetic medicines for prevalent diseases. Our values - Rewrite the future, On the Cutting Edge, Better Together, Dynamically Different, Kindness and Integrity form the fabric of the organization. They are reinforced daily and serve as key dimensions in the hiring process to help us ensure that Korro is a magnet for outstanding talent and a great place to work. Join us as we redefine what's possible in genetic medicine and work to make a lasting impact on human health.


The Position:

We are seeking a motivated, innovative and collaborative Sr. Scientist with expertise in Drug Metabolism and Pharmacokinetics (DMPK) supporting the discovery and development of oligonucleotide-based drug therapeutics (ONT). This candidate will play a key role in understanding the delivery, distribution, metabolism, excretion and PK/PD relationships of drug candidates against therapeutically relevant targets. The key contributions for this position will be the bioanalysis and biotransformation of ONTs to help advance our early research efforts to preclinical development. The candidate should have a proven track record in the field of DMPK with extensive hands-on experience and thorough understanding of oligonucleotide bioanalysis and different delivery systems. This position will have the opportunity to work as the DMPK expert within cross-functional high performing teams to translate research findings into novel therapeutic strategies to support clinical drug development. The successful candidate will join an interdisciplinary DMPK team within a growing biotech company at the cutting edge of RNA research. This candidate will have potential for significant career growth at Korro and will contribute positively to its developing culture. This position reports to the Head of DMPK and will be based in our Cambridge, MA.


Job Responsibilities:
  • Contribute to the bioanalytical and biotransformation strategy.
  • Design, plan, and execute assays to understand the biodistribution, pharmacokinetic and metabolic properties of novel ONTs with multiple mechanisms of delivery.
  • Be proficient in ligand binding assays, LC-MS/MS, HRAM and automation platforms.
  • Actively keep up to date with the ongoing research in the field and apply novel assays to achieve goals related to building DMPK understanding from Research through Development.
  • Cross-functional collaboration with Biology, Delivery, Chemistry, and In Vitro and In Vivo Pre-clinical Pharmacology teams to advance Korro Bio’s early research activities to preclinical development.
  • Independently run laboratory experiments to support and advance discovery efforts.
  • Mentor and train junior scientists.
  • Multi-task across several projects and manage time effectively to achieve results.
  • Design and write protocols, perform experiments, organize and analyze data, interpret results, record experiments in an electronic lab notebook, and summarize work in presentations and technical reports.
  • Adhere to all laboratory safety requirements and standard operating procedures, help maintaining general laboratory functionality, including lab equipment maintenance and the ordering, and receiving of lab supplies. 
  • Other duties as assigned. 


Qualifications:
  • Degree in pharmaceutical sciences, analytical chemistry, molecular biology or related discipline.  BS or MS with at least 6-8 years of experience in the pharmaceutical industry or PhD with at least 4 years of experience working with bioanalysis of oligonucleotide therapeutics.
  • Hands on-assay development experience with different bioanalytical assay formats and broad in-depth knowledge of regulatory requirements.  Strong assay troubleshooting, data analysis and interpretation skills.
  • Knowledge and experienced in bioanalysis within ADME/DMPK, metabolite identification, biodistribution and how DMPK fits into the larger picture of drug discovery and development.
  • Experience conducting cellular assays with cell culture.
  • Relevant project representation experience in cross-collaborative program teams as a DMPK expert.
  • Excellent interpersonal and communication skills in a variety of settings, ability to share and discuss scientific data clearly to peers and to senior leadership.
  • Team oriented and collaborative approach to work across multiple teams.
  • Attention to detail, critical analysis of data/reports, and troubleshooting abilities.
  • Proven ability to achieve results, keep projects on timeline, and find solutions as needed to ensure that project deliverables are met.
  • Experience managing direct reports and CRO resources is a plus.


Benefits:  Korro offers competitive compensation, including equity-based compensation, and a comprehensive benefits package that includes medical, dental, vision, 401(k) retirement plan, life insurance, a dependent care flexible spending account and a Company-funded health savings account and free parking.

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Average salary estimate

$135000 / YEARLY (est.)
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$120000K
$150000K

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What You Should Know About Senior Scientist, Korro Bio

Are you ready to make waves in the world of genetic medicine? Join Korro as a Senior Scientist, and be part of a dynamic team pushing the boundaries of drug metabolism and pharmacokinetics (DMPK) in Cambridge, MA. At Korro, we are on a mission to develop innovative RNA editing therapies for both rare and prevalent diseases, revolutionizing the way we think about genetic treatments. As a Senior Scientist, you will dive deep into the bioanalysis and biotransformation of oligonucleotide-based therapeutics, working collaboratively across high-performing teams to translate research into impactful clinical strategies. Your hands-on expertise in DMPK will be pivotal as you plan and execute assays, analyze pharmacokinetic properties, and mentor junior scientists. Here, we actively cultivate an environment where creativity and collaboration thrive, all underpinned by our core values of Kindness, Integrity, and striving to Rewrite the Future. If you have a proven track record in the pharmaceutical field and a passion for advancing genetic medicine, Korro is the perfect place to take your career to the next level. Join us as we embark on this transformative journey, empowering patients and redefining what’s possible in healthcare.

Frequently Asked Questions (FAQs) for Senior Scientist Role at Korro Bio
What are the responsibilities of the Senior Scientist at Korro?

The Senior Scientist at Korro is responsible for contributing to the bioanalytical and biotransformation strategy, designing and executing assays, and understanding the pharmacokinetic and metabolic properties of oligonucleotide therapeutics. Additionally, the role involves cross-functional collaboration, mentoring junior scientists, and maintaining laboratory safety and operational standards.

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What qualifications do I need for the Senior Scientist position at Korro?

To qualify for the Senior Scientist role at Korro, candidates should possess a degree in pharmaceutical sciences, molecular biology, or a related field. A BS or MS with at least 6-8 years of experience or a PhD with 4 years of relevant bioanalysis expertise in oligonucleotide therapeutics is required. Strong communication, teamwork, and project management skills are essential, alongside a proven ability to troubleshoot and analyze complex data.

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What skills are important for a Senior Scientist at Korro?

Key skills for a Senior Scientist at Korro include proficiency in various bioanalytical assay formats, strong assay troubleshooting abilities, in-depth knowledge of ADME/DMPK principles, and experience in collaborating cross-functionally. Competence in laboratory techniques like LC-MS/MS and HRAM, as well as excellent interpersonal skills, are crucial for success in this role.

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What kind of work environment can I expect at Korro as a Senior Scientist?

At Korro, the work environment is collaborative and innovation-driven. As a Senior Scientist, you will engage with interdisciplinary teams focused on breakthrough genetic research. The company values individual contributions and fosters a culture of open communication, respect, and kindness, ensuring that everyone’s input helps shape the future of genetic medicine.

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How does the Senior Scientist role at Korro contribute to drug development?

The Senior Scientist role at Korro is crucial in the early stages of drug development, focusing on the bioanalysis and pharmacokinetics of oligonucleotide therapies. By executing complex assays and collaborating with diverse teams, the Senior Scientist helps translate research findings into actionable strategies that assist in bringing innovative medicine to patients.

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Common Interview Questions for Senior Scientist
Can you describe your experience with bioanalytical assays related to oligonucleotide therapeutics?

When answering this question, highlight specific techniques and assays you've developed or supported in your past roles. Emphasize your hands-on experience and any successful projects that demonstrate your expertise and understanding of oligonucleotide bioanalysis.

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How do you stay updated with current research in pharmacokinetics and drug metabolism?

Discuss your strategies for continuous learning, including reading scientific journals, attending conferences, or being part of professional organizations. Mention any specific research topics or findings that have influenced your work.

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What strategies do you use for effective collaboration in cross-functional teams?

Highlight your communication skills and collaborative strategies, focusing on how you facilitate discussions and share insights among diverse teams. Provide examples of successful teamwork that led to significant outcomes in your projects.

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How do you approach designing experiments for pharmacokinetic studies?

In your response, detail the steps you take to plan an experiment, including hypothesis formulation, method selection, and how you ensure rigorous data collection and analysis. Showcase a specific experiment you designed and what you learned from it.

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Can you provide an example of a challenging project you led and how you overcame obstacles?

Share a detailed story of a past project, outlining the challenges encountered and the innovative solutions you implemented. Emphasize your leadership skills and how you guided your team towards success.

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What experience do you have with LC-MS/MS and other analytical platforms?

Explain your hands-on experience with LC-MS/MS systems, detailing specific applications in studies you've conducted. If applicable, mention any troubleshooting you performed and improvements you made to streamline data collection.

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How do you prioritize tasks when managing multiple projects?

Describe your time management techniques, perhaps using tools like project management software or to-do lists. Provide an example where you successfully managed multiple projects and kept them on schedule.

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What do you consider critical when interpreting data from DMPK studies?

Discuss the important factors in data interpretation, such as acknowledging variability, understanding biological relevance, and ensuring statistically sound conclusions. Provide insights on how you've applied these principles in your work.

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How do you mentor junior scientists in DMPK-related tasks?

Talk about your mentoring philosophy, how you approach teaching complex concepts, and the methods you use for training. Share a memorable mentoring experience that resulted in noticeable improvement in a junior colleague's skills.

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What do you believe is the future of oligonucleotide therapeutics?

Offer your perspective on advancements in oligonucleotide therapies based on current trends and research. Discuss how you envision these innovations impacting patient care and the pharmaceutical landscape.

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DATE POSTED
December 23, 2024

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