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Vice President/ Senior Vice President, Clinical Development

Boston, MA

The Organization

What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible.

Our Endosomal Escape Vehicle (EEV™)-therapeutics are designed to enable the efficient intracellular delivery of a wide range of therapeutics into a variety of organs and tissues, resulting in an improved therapeutic index. Through this proprietary, versatile and modular approach, Entrada is advancing a robust development portfolio of RNA-, antibody- and enzyme-based programs for the potential treatment of neuromuscular, ocular, metabolic and immunological diseases, among others.

Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne who are exon 44, 45 and 50 skipping amenable. We have also partnered to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1.

We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.

Responsibilities

  • Provide oversight and leadership of clinical programs including strategic planning, execution, and completion of clinical trials according to all applicable regulations and guidance, ICH/GCP, and Entrada SOPs.
  • Support growth and management of Clinical Development function, including oversight of clinical leads, biostatistics, clinical pharmacology and biomarkers.
  • Partner with Clinical Operations to ensure all clinical study activities are completed in accordance with applicable regulations and guidance; ICH/GCP, and Entrada SOPs.
  • Review clinical data from all phases of development and assist in generating study reports and publications.
  • Serve as study medical monitor, as needed.
  • Develop and maintain relationships and serve as the main medical liaison with key opinion leaders and Principal Investigators.
  • Represent Entrada’s clinical team in interactions with regulatory agencies.
  • Provide management personnel with timely updates on progress and changes in scope, schedule, and resources as required.
  • Ensure compliance with all applicable regulatory standards related to global clinical trials and interactions with physicians.
  • Collaborate closely with internal research team to integrate translational research into development and clinical strategies, and regulatory submissions.
  • Responsible for the clinical content of all clinical and regulatory documents, including protocols, INDs, CTAs, investigator brochures, CRF’s, annual IND reports, CSR’s, ISS’s, ISE’s, and clinical expert reports.
  • Organize and present at relevant clinical advisory boards, data monitor committees and medical/scientific meetings.
  • Travel nationally and internationally, as needed.

The Necessities

At Entrada, our passion for science, our devotion to patients and our values drives our behavior:

  • Humanity - We genuinely care about patients and about one another.
  • Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.
  • Creativity - We are creative problem solvers.
  • Collaboration - We are more than the sum of our parts.
  • Curiosity - We have a growth mindset and push conventional thought and theory.

To thrive on our team, you will need to come with:

  • MD or DO (physician) required, preferences for formal training in neuromuscular disease.
  • 10+ years of industry experience.
  • Experience with clinical development in Neurology/Neuromuscular disorders.
  • Strong scientific background.
  • Strong project planning, leadership, negotiation and presentation skills as well as an ability to contribute creative yet practical solutions to problems.
  • Experience with all aspects of management of clinical trials from inception to completion across all phases of development including study design.
  • Experience in communicating/presenting key/complex information to department/functional lead(s)/senior management.
  • Strong knowledge of FDA and ICH regulations.
  • Expert knowledge of Good Clinical Practice (CGP).
  • Ability to multi-task and manage several projects in parallel, paying attention to detail.
  • Ability to forge cross-functional working relationships with internal teams and external project partners.
  • Ability to be proactive in identifying issues and hurdles that may hinder the effective implementation of the trial and resolve the issues in a timely fashion.

The Perks

By becoming a team member here at Entrada, you’ll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. We also offer a generous transportation stipend to commute as you wish. Our location in the vibrant and growing Seaport District is close to all the best that the city of Boston has to offer.

Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.

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