Cabaletta Bio

Manager or Sr. Manager of Translational Medicine

Cabaletta Bio$100K — $130K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • MS/PhD with 3+ years or BS with 5+ years in pharma/biotech.
  • Strong grasp of drug development and clinical trial design.
  • Hands-on experience in vendor management and financial planning.
  • Basic knowledge of US and EU regulatory processes preferred.
  • Excellent leadership and interpersonal communication skills.

Responsibilities

  • Lead vendor selection and manage relationships for clinical trials.
  • Establish and manage vendor contracts for ongoing trials.
  • Identify and evaluate novel translational vendors for assay development.
  • Manage vendor relations to ensure regulatory compliance across locations.
  • Support regulatory submissions for early-phase clinical programs.
  • Facilitate technology transfer and oversee validation of assays.
  • Collaborate with clinical teams for successful study execution.
  • Attend conferences to stay updated on trends in translational medicine.

Benefits

  • Competitive benefits and paid time off (PTO).
  • Stock option plans.
Full Job Description
Manager or Sr. Manager, Translational Medicine

Hybrid - Philadelphia

Manager or Sr. Manager, Translational Medicine

Hybrid - Philadelphia

About the position:

The Manager or Sr. Manager, Translational Medicine will report to the Director, Translational Medicine and will be responsible for leading key external vendor relationships, budgeting for external workstreams, and planning for new translational workflows within existing or new clinical programs. They will work closely with the operations team within the Translational group to support ongoing testing requests at external vendors. Additionally, they will assist in the authoring, data verification, and timeline management of early phase regulatory submissions.

Responsibilities:

  1. Lead new vendor selection and manage ongoing vendor relationships necessary to support early phase and registrational clinical trials in the United States and within ex-US countries. Align heavily with Clinical Operations, Clinical Development, Regulatory Affairs and Quality Assurance on these partnerships.
  2. Establish new and manage existing vendor contracts and alliance to drive development of ongoing and future trials.
  3. Identify and vet novel translational vendors to support assay transfer and manage bespoke assay development.
  4. Manage translational vendor relations and strategy across US and ex-US sites to ensure compliance and consistency across regulatory and quality.
  5. Support bespoke and annual regulatory submissions supporting early Phase clinical programs within the US and ex-US. Where necessary, support new clinical trial protocol development alongside the Clinical Development and Regulatory teams at Cabaletta.
  6. Working closely with subject matter experts within the Translational Medicine scientific team, facilitate technology transfer of key correlative assays from Cabaletta to external vendors. Oversee timelines and execution of assay validation, data generation, data transfer processes, and data interpretation.
  7. Collaborate with cross-functional clinical operation study teams to ensure the successful execution of clinical studies and the timely delivery of high-quality study results.
  8. Attend scientific conferences, meetings, and workshops to keep up to date with the latest developments in the field of translational medicine, vendor management and contribute to scientific publications.


Qualifications:

  • MS/PHD in a relevant field along with a minimum of 3+ years of relevant experience in the pharmaceutical or biotech industry or BS with a minimum of 5+ years of relevant experience.
  • Strong understanding of drug development and clinical trial design, as well as experience in the interpretation and analysis of translational data.
  • Prior hands-on experience with vendor management, contracting, legal discussions, and financial planning.
  • A basic understanding of the regulatory process in the US and EU, is preferred.
  • Excellent leadership, communication and interpersonal skills, and the ability to work effectively in a cross-functional team environment.Top of Form
  • Strong team orientation, collaborative skills, and passion for continuous self-development.
  • Experience in industry or in a startup industrial setting is preferred.
  • Background or relevant work experience in immunology or cell therapy is preferred.
  • High level of flexibility to support various other activities the ability to learn new techniques outside of existing field of expertise is ideal.
  • Highly motivated self starter


Our name - Cabaletta - is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression.

For more information, please visit https://www.cabalettabio.com/join-our-crew

Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans.

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About Cabaletta Bio

Size
56 employees
Market Cap
$243.8 million
Industry
Net Income
-$29.4 million
Founded
2017
NASDAQ

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