Director / Senior Director, Clinical Operations

ZAG BIO INC

Director / Senior Director, Clinical Operations

Cambridge, MA
Full Time
Paid
  • Responsibilities

    Benefits:

    401(k)

    401(k) matching

    Bonus based on performance

    Competitive salary

    Dental insurance

    Flexible schedule

    Health insurance

    We are seeking an experienced and highly motivated Director / Senior Director of Clinical Operations to lead the operational execution of the Company’s first clinical program in Type 1 diabetes as it advances into early-phase clinical trials. Reporting to the Chief Medical Officer, this individual will play a critical role in building and executing clinical operations strategy in a fast-paced, start-up environment.

    The successful candidate will embrace a hands-on ethos, thrive in ambiguity, and bring a pragmatic, detail-oriented approach to trial execution. This role will work closely with cross-functional colleagues across clinical development, regulatory, translational science, and external partners.

    Job Responsibilities

    Reporting to the Chief Medical Officer, the incumbent will be responsible for the planning, execution, and oversight of early-phase clinical trials, with responsibilities including:

    Lead clinical operations strategy and execution for first-in-human and early-phase clinical studies in Type 1 diabetes

    Develop and maintain integrated clinical trial plans, timelines, budgets, and risk mitigation strategies

    Provide operational input into clinical development plans, study protocols, and investigator brochures

    Select, manage, and oversee CROs, vendors, and other external partners to ensure delivery against scope, timeline, budget, and quality expectations

    Oversee site feasibility, selection, initiation, monitoring, and close-out activities

    Ensure trials are conducted in compliance with GCP, SOPs, and applicable regulatory requirements

    Support preparation of clinical sections of regulatory submissions, including INDs, amendments, and interactions with regulatory authorities

    Additional responsibilities include:

    Day-to-day operational oversight of clinical trial conduct, including issue resolution and proactive risk management

    Development and implementation of clinical operations processes, templates, and SOPs appropriate for a growing organization

    Management of clinical trial budgets, forecasts, and vendor invoices

    Contribution to clinical governance activities, including internal reviews, data reviews, and study team meetings

    Support investigator engagement and communication, including KOL interactions as appropriate

    Maintain accurate and inspection-ready trial documentation (eTMF, trial master files, vendor records)

    Participate in cross-functional planning to support pipeline expansion and future clinical programs

    Required Qualifications and Experience

    Bachelor’s degree in life sciences or related discipline; advanced degree preferred

    10+ years of progressive clinical operations experience in biotech and/or pharmaceutical industry, with increasing responsibility for trial execution

    Hands-on experience leading early-phase (Phase 1 and/or Phase 1b/2) clinical trials

    Strong working knowledge of GCP, ICH guidelines, and FDA regulatory requirements

    Demonstrated experience managing CROs and external vendors in a sponsor-oversight role

    Ability to operate independently in a small company environment with limited infrastructure

    Excellent organizational, communication, and problem-solving skills

    Willingness to be both strategic and highly execution-focused

    Preferred Qualifications:

    Prior experience supporting clinical programs in immunology, autoimmunity, endocrinology, or metabolic diseases

    Experience contributing to IND submissions and early regulatory interactions

    Prior experience in a start-up or emerging biotech environment

    Zag Bio values the diversity of our workforce and maintains a deeply respectful, values-driven working environment. We are committed to equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law.

    We are not accepting unsolicited resumes from employment agencies for any employment opportunities at this time.

    Flexible work from home options available.