Senior Director, Head of Clinical Operations

ABOUT US

There are more than 9 million immunocompromised people in the United States. Almost half a million of those represent a population that are moderately to severely immunocompromised and at highest risk for severe COVID-19, including stem cell and solid organ transplant patients as well as those with hematologic cancers.

At Invivyd, Inc., we take those numbers very seriously and we come to work each day on a mission to deliver protection from serious viral infectious diseases, beginning with SARS-CoV-2. Invivyd deploys a proprietary integrated technology platform unique in the industry designed to assess, monitor, develop, and adapt to create best in class antibodies.

In March 2024, Invivyd received emergency use authorization (EUA) from the U.S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates.

In October 2025, the FDA cleared the company's Investigational New Drug (IND) application and provided feedback to advance the company's REVOLUTION clinical program, Invivyd's development program for VYD2311, a vaccine alternative monoclonal antibody being investigated for the prevention of COVID-19.

Be part of making a difference. Be part of Invivyd.

Location: New Haven, CT (Northeast preferred)

Invivyd's headquarters is in New Haven, CT. This role will be hybrid with a mix of both onsite (New Haven, CT) and remote working.

Position Summary:

The Head of Clinical Operations reporting to the Head of Clinical Development will provide strategic operational guidance to ensure that clinical trials are properly planned and executed across all clinical stage programs. In addition, the incumbent will oversee all aspects of clinical trial execution, including GCP compliance on studies supporting the development of novel monoclonal antibodies aimed at preventing the transmission of and/or treating of infectious diseases, including SARS CoV-2.

Responsibilities:

• Oversee study management activities for global monoclonal antibody clinical research studies

• Responsible for clinical trial management activities on specified study in addition to local and global CRO oversight

• Lead selection and management / oversight of external vendors; develop standard vendor specifications; review vendor reports, budgets and forecasts, and metrics

• Review and negotiate contracts

• Forecast costs for clinical studies

• Review and approve invoices against approved budget/contract

• Monitor subject accrual and study progress via standard reports

• Oversee clinical monitoring from site qualification to site closure visits and ensure integrity of clinical data with respect to accuracy, accountability, and documentation through review of monitoring reports and completed case report forms

• Update program team and Clinical Operations management on timelines and progress toward milestones

• Apply Invivyd and industry standards across research program(s)

• Provide guidance to Clinical Operations Leads in oversight of vendors and investigators to ensure compliance with the study protocol and overall clinical objectives

• Collaborate with study leads to establish performance and quality metrics for the study and report metrics and that drive quality and efficiency

• Work with Clinical Operations/Development management to support timely and in-budget completion of department goals by ensuring compliance and continuity with relevant SOPs and organizational work instructions

• Support departmental initiatives aimed at innovation, process improvement, and efficiency

• Develop or contribute to key vendor oversight plans and processes

• Assist with the development of standard operating procedures (SOPs), work instructions (WIs), and standardized forms to define Clinical Department processes

• Collaborate with Clinical, Regulatory, Safety, Quality, and other functional team members to ensure compliance of department/study activities with FDA regulations, guidelines, and principles of ICH GCP and Invivyd SOPs

• Ensure GCP compliance by providing guidance and support to Clinical study leads and Clinical Study Teams

• Support activities associated with QA audits: as needed, assist the clinical trial teams in responding to audit findings, ensuring appropriate root cause is performed and CAPAs are created; ensure all items are documented appropriately

• Manage direct reports, as applicable

• Limited travel (<20%) for site and vendor oversight

Requirements:

• Minimum education and experience: Bachelor’s degree with 10-15 years relevant experience

• Global study management at sponsor company

• Strong oral and written communication skills

• Experience with development and maintenance of study timelines and budgets

• Highly adaptable, proactive, deadline and detail-oriented

• High level of professional expertise through recent industry training and familiarity with good clinical practice and risk-based quality management best practices

• The candidate will work in a fast-paced and dynamic environment

• Ability to accommodate hybrid schedule with a mix of both onsite (New Haven, CT once a month) and remote working

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At Invivyd we strive to create a welcoming and inclusive environment. Here all applicants will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics.

Invivyd is proud to be an equal opportunity employer.

We do not accept unsolicited resumes from agencies.