Program Manager II- Site Activations - Cambridge

We are seeking a Program Manager II, Site Activations to own and scale the site activation process across the organization. This role is responsible for driving on-time site activations within SLAs, proactively identifying and resolving blockers, · Maintain clear activation plans ...

· Manage all project team activities related study start up, conduct and close out activities. · Work with Outsourcing and Contracts Management to ensure Site Contracts reflect trial activities and related budget. · ...

The Senior Clinical Monitoring Lead will serve as the lead CML for complex studies involving multiple Clinical Monitoring Leads. · Ensure efficient and thorough study feasibility,Ensure timely site initiation,Clinical study set up activities coordination oversight responsibilitie ...

When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives. · All candidates should make sure to read the following job description and information carefully before applying. · Physician Hospitalist Job Description: Ready to jo ...

We are pioneering the application of powerful artificial intelligence tools to the practice of cardiology and drug development. · Demonstrate advanced knowledge of clinical research processes and tools. · Serve as a subject matter expert on clinical research workflows. · ...

We are seeking a Clinical Regulatory Specialist to join our team at Iterative Health. · Working alongside research sites on essential regulatory document completion. · Facilitating clinical trial regulatory activity from study start-up through closeout. · ...

+The Director Regulatory Site CMC ensures efficient and compliant management of regulatory change control and post-approval activities at the site level. · Lead site-specific post-approval change management activities... · ...

We are seeking an experienced Strategic Account Liaison to lead the development and execution of strategies that support site selection, readiness and site activation to deliver our transformative CRISPR therapy to patients. · ...

We are seeking a Clinical Regulatory Specialist to join our team. The Clinical Regulatory Specialist will work under the direction of the Chief of Staff with the primary responsibility of assisting research sites with the conduct and compliance of Phase 2-4 pharma-sponsored resea ...

Coverage Needed · March 16, August 28, 2026 · Schedule: Monday through Friday, Clinic hours between 7am and 5pm, Variable clinic sessions · Coverage Type: Locum · Clinical Details · Call: 1/3 weekend and rotating evening coverage · EMR: EPIC · Support Staff: Two rheumatologists a ...

The Site Relationship Manager will be responsible for overall US site management training and quality oversight of assigned studies exploring new technologies to generate collect and present patient data within clinical practice setting. · ...

We want all of our people to go beyond what is possible. · We aren't constrained by typical end rails, · and we aren't out to just treat people. · We're all in this for something more. · We're driven to cure and motivated for change.Beyond our science, · we live our four core val ...

We are seeking an experienced and visionary National Strategic Accounts Team Lead to lead the enablement and optimization of treatment sites delivering our transformative CRISPR therapy to patients. · Build, lead, and mentor a high-performing team of Strategic Account Managers fo ...

We want all of our people to go beyond what is possible. We aren't constrained by typical end rails, and we aren't out to just “treat” people. · We're all in this for something more. We're driven to cure and motivated for change. ...

· Why Join Intellia?  · Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.  · Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel s ...

Support the Clinical Operations Study Leader and team in managing clinical trials. · ...

Clinical Research Associate Lead for Ipsen in Cambridge MA. Responsibilities include coordinating and monitoring clinical studies, ensuring timely delivery and quality standards. · Minimum experience of 2 years in clinical monitoring activities of international clinical developme ...

Su función será apoyar al líder operativo de estudios clínicos y su equipo en la gestión y supervisión de ensayos clínicos. Reporta a un director asociado de operaciones clínicas (o superior). · Asistirá en la ejecución diaria del ensayo: inicio del sitio, inscripción, monitoreo ...

Support the design execution and regulatory submission of clinical studies for hospital monitoring devices to ensure safety effectiveness and compliance. · Provide strategic guidance on clinical study protocol design. · Develop and implement clinical development plans and data co ...

Clinical Development Lead to focus on study design strategy for the development of clinical study protocols and support the clinical operations team with study execution. · ...