Associate Director Clinical Operations

Soufflé Therapeutics is a biotech company focusing on the cell-type specific delivery of genetic medicines. It's team of driven scientists is making a mark in delivery of oligonucleotides to extrahepatic tissues. We thrive in a purpose-building lab and office space in Watertown. Come and join us in our quest! Soufflé Therapeutics is launching a new clinical program, and we're looking for an Associate Director of Clinical Operations to help build it from the ground up. This is a rare chance to shape a study from first principles: you won't inherit someone else's playbook, you'll write it. As the second member of a growing Clinical Ops team, you'll partner directly with our Senior Director and cross-functional leaders across Preclinical, Regulatory, and CMC to take an early-phase study from start-up through close-out. If you thrive on ownership, love the scrappy energy of a "department of three," and want your fingerprints on every stage of a trial, this role is built for you. Key Responsibilities Own end-to-end execution of one or more early-phase clinical studies, serving as the operational lead from study start-up all the way through close-out and the final Clinical Study Report Build and manage day-to-day relationships with CROs, clinical sites, central labs, and vendors to keep deliverables high-quality and on schedule Lead site start-up, patient enrollment, monitoring, and protocol compliance with a hands-on, accountability-driven approach that keeps studies moving Author and/or review key clinical documents, including informed consent forms, pharmacy manuals, and other trial-related materials Ensure timely collection of clinical data, samples, and lab results across all active study sites What Success Looks Like In 3 months: You've gotten fluent in the protocol and study design, built relationships with key stakeholders, and are actively helping author and/or review core study documents and driving study start-up activities end to end, from site feasibility and selection through initiation and vendor onboarding In 6 months: You're leading independently every aspect of the study, including sites, CROs, and vendors like labs and imaging partners, with full command of the program In 12 months: You're managing all aspect of the study, including multiple sites, CROs, and vendor and supporting life cycle management studies, supporting next studies/other programs as needed Qualifications — Required 8+ years of experience in clinical operations, including 2-3 years in a Senior Manager or comparable role (Associate Director level at a similar-sized company) Broad working knowledge of global regulations and guidelines, including CFR, ICH GCP, HIPAA, and GDPR Excellent problem-solving, leadership, and communication skills. Ability to work in a fast paced cross-functional team. Demonstrated experience leading or starting the studies Experience leading global clinical trials (non-US EU/UK and Australia). Qualifications — Preferred Experience leading US clinical trials Early Clinical Trial Experience Education Bachelor's degree (BA/BS) required At Soufflé Therapeutics, we are intentional about building an equitable culture. How we treat our people is reflective of this focus. Our pay structure is base salary + bonus + equity. This is an onsite position in Watertown, MA (US) with flexibility as needed for collaboration and external engagements. We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. #J-18808-Ljbffr