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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- and protein-based programs for the potential treatment of neuromuscular and ocular diseases, among others.
Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne who are exon 44, 45, 50 and 51 skipping amenable. Entrada has 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.
You’re a passionate patient advocacy professional with experience engaging, supporting, and collaborating with advocacy groups and the communities they represent. You love building relationships, hearing new perspectives, and finding ways to turn those insights into meaningful actions that can influence planning and decision-making company wide. You’re highly organized and eager to make initiatives come to life. You “sweat the details” to make sure work is credible, compliant, and compassionate. You thrive in a fast-paced, mission-driven environment and are ready to help build an industry-leading advocacy function.
We are unwavering in our in our dedication to engaging patient communities every step of the way, forging partnerships that allow us to deeply understand their perspectives and priorities and develop innovative medicines that truly address their needs.
With three distinct Duchenne programs moving into global clinical development by the end of 2025, another in 2026, and our expanding work in Ocular—these are exciting times for Entrada. Reporting directly to the Senior Director of Patient Advocacy, you’ll help develop and implement advocacy programs and partnerships across our programs that enable us to learn from patient communities and shape our decision-making.
At Entrada, our passion for science, our devotion to patients and our values drives our behavior:
To thrive on our team, you will need to come with:
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.
Entrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.
Entrada Therapeutics, Inc. (the “Entrada,” “we,” “us,” or “our”) respects your privacy and we want you to be familiar with how we collect, use, share, or otherwise process, your Personal Information. Please reference our privacy statement here to understand how and when your data is being used.
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