Source Job

• Oversee evidence-generation strategy and manage research studies for the da Vinci Cardiac Surgery Program.
• Collaborate with stakeholders to identify evidence gaps, align priorities, and develop evidence-generation plans.
• Manage CROs, research partners, and publications while ensuring regulatory compliance and audit readiness.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, with technologies like the da Vinci system transforming care for millions worldwide. We are a team of engineers, clinicians, and innovators united to make surgery smarter, safer, and more human.

• Lead clinical research project planning, execution, and delivery, ensuring regulatory compliance and quality.
• Coordinate cross-functional teams and manage timelines, budgets, and study documentation.
• Serve as the primary sponsor and client contact, providing regular project updates and resolving issues.

Alimentiv is a global CRO advancing therapies for gastrointestinal diseases, with deep expertise in IBD drug development. With about 700 employees across multiple countries, it is a private, profit-with-purpose company focused on scientific research and its people.

• Support the planning, coordination, and delivery of clinical research studies.
• Collaborate with sponsors, cross-functional teams, vendors, and clinical sites to ensure studies meet timeline, budget, and quality targets.
• Manage project milestones, site activation, patient recruitment, and risk mitigation in a remote working environment.

Jobgether is an AI-powered job matching platform connecting candidates with hiring companies. The hiring partner is a science-driven clinical research organization offering a collaborative remote environment.

• Serve as primary point-of-contact liaison with clients and oversee all aspects of clinical trials.
• Manage study budgets, project timelines, risk, and cross-functional teams to ensure quality and compliance.
• Drive bid defense preparation, client presentations, and continuous process improvement across assigned portfolios.

Precision for Medicine supports clinical research and development for biopharmaceutical and life science companies. It is a global, collaborative organization that emphasizes quality, innovation, and professional growth.

• Coordinate planning, implementation, and delivery of device logistics projects for eCOA clinical trials.
• Oversee budgets, deployment plans, and risk mitigation while collaborating with clinical teams and stakeholders.
• Ensure inventory management, mobile device management, and global shipping are completed on schedule and within scope.

The hiring company is a life sciences organization specializing in device logistics and electronic clinical outcome assessments for clinical trials. They foster a collaborative, cross-functional remote culture aligned with US East Coast time zones.

• Direct and manage a team of Project Directors and Project Managers in global project delivery.
• Provide leadership and oversight for clinical programs and act as primary escalation point for sponsors.
• Optimize profitability, manage resources, and ensure compliance with quality standards and regulations.

Precision Medicine Group provides clinical research and project management services for global clinical trials. The company promotes a culture centered on quality, people, clients, and performance.

• Collaborate with project teams to support study startup and serve as primary point of contact for clinical sites.
• Provide training on Beacon's devices and protocols, monitor progress, and maintain GCP/ICH compliance.
• Address operational issues via Zendesk and Asana and deliver actionable site feedback for workflow improvements.

Beacon Biosignals is transforming precision medicine for the brain with at-home EEG and cardiopulmonary monitoring platforms for clinical development and diagnostics. They foster a remote-first culture with hubs in Boston, New York, and Paris, emphasizing curiosity, simplicity, and empathy.

• Drive SimNow 2 simulator implementations and upgrades, coordinating cross-functional activities.
• Interface between customer IT/OR staff and Intuitive service teams to schedule and execute upgrades.
• Ensure documentation and clear status/risk communication to stakeholders and EU leadership.

Intuitive is a pioneer in robotic-assisted surgery, expanding physicians' potential to heal through intelligent technology. With a diverse, inclusive team of over 25 years, we work globally to solve healthcare's hardest challenges.

• Lead the development and execution of industry-sponsored research and quality improvement programs.
• Collaborate with internal and external stakeholders to drive strategic partnerships and evidence generation.
• Oversee project budgets, timelines, and cross-functional teams to ensure successful delivery.

The American Heart Association is a nonprofit organization dedicated to fighting heart disease and stroke through research, education, and advocacy. It is a large national organization with a culture focused on work-life harmonization and employee well-being.

• Manage integrated CMC timelines and drive alignment across technical, clinical, and regulatory teams.
• Coordinate CDMO/CMO deliverables, budgets, and regulatory submission milestones.
• Facilitate cross-functional meetings, track risks and action items, and provide clear program visibility.

Pulmovant is a clinical-stage biotechnology company focused on developing treatments for pulmonary diseases, with a lead candidate for pulmonary hypertension associated with interstitial lung disease. As part of the Roivant family, it fosters a collaborative and innovative culture, leveraging resources to advance its pipeline.

• Coordinate participant recruitment start-up activities for assigned clinical trials.
• Manage sponsor-funded marketing budgets and track expenditures to optimize ROI.
• Liaise with vendors, sponsors, and regulatory bodies to ensure compliant campaign launches.

Headlands Research is a leading network of advanced clinical trial sites that leverages technology and support services to enhance clinical trial delivery and community outreach. Founded in 2018, the company operates 20+ sites across the US and Canada and is rapidly growing.

• Develop and maintain integrated project plans for global regulatory submissions, ensuring adherence to scope, timelines, budgets, and quality standards.
• Act as the primary regulatory timeline contact across Clinical, Nonclinical, CMC, Quality, and Commercial functions, fostering collaboration and alignment.
• Identify and mitigate project risks, prepare teams for agency meetings, and lead responses to regulatory queries from global health authorities.

Centessa Pharmaceuticals is a clinical-stage company developing orexin receptor 2 agonists for narcolepsy and other sleep-wake disorders. As a wholly owned subsidiary of Eli Lilly and Company, it shares a culture of caring and impact with over 50,000 employees.

• Lead end-to-end project lifecycle for multiple global market research projects, from bid to invoice, ensuring on-time, on-budget delivery.
• Serve as client partner, managing expectations, providing proactive recommendations, and identifying risks or opportunities.
• Oversee operational execution including survey programming, vendor management, field reporting, and quality control.

Konovo is a global healthcare intelligence company on a mission to transform research through technology. With a workforce of over 300 employees across 5 countries, we collaborate to support some of the most prominent names in healthcare.

• Manage an assigned portfolio of clinical research technology customers, building trust and driving strategic account plans.
• Lead onboarding, adoption, and training to help research sites maximize value from the clinical trial management platform.
• Drive retention and revenue growth through renewals, expansion opportunities, and cross-functional collaboration.

This partner company provides innovative clinical trial management technology for healthcare and clinical research organizations. They foster a collaborative, inclusive, and technology-driven culture with multidisciplinary teams.

• Lead global clinical study delivery, overseeing project management and finance teams to execute full-service trials.
• Drive operational planning, resource allocation, and financial risk oversight as part of senior leadership.
• Represent project operations with sponsors and business development, ensuring quality, compliance, and best practices.

Alimentiv is a global contract research organization focused exclusively on advancing therapies for gastrointestinal diseases, supporting over 70% of IBD compounds in development. With approximately 700 employees across multiple countries, it operates as a private, profit-with-purpose company investing in research, technology, and its people.

• Execute global clinical trials from inception through closure, supporting study-level oversight and cross-functional collaboration.
• Manage external vendors, including RFP/initiation, scope of work, deliverable oversight, and risk management.
• Drive recruitment management, study materials development, and system management for CTMS, eTMF, EDC, IRT, and ePRO.

AbbVie discovers and delivers innovative medicines and solutions across key therapeutic areas like immunology, oncology, and neuroscience. As a global biopharmaceutical company, it operates with integrity, drives innovation, and fosters a collaborative culture to transform lives.

• Work with RPI teammates to translate research initiatives into actionable project plans.
• Manage full project life cycles including scope, resources, risks, issues, and timelines.
• Drive multiple concurrent research and process-improvement projects across the RPI portfolio.

ESO is a data, technology, and research company passionate about improving community health and safety through the power of data. We are a fast-paced, growing organization serving thousands of EMS, fire, and hospital customers across the US, Canada, and Northern Ireland, with a culture that is nimble, fun, and committed to bringing your true self to work.

• Manage regulatory submissions and site activation readiness across the UK.
• Negotiate budgets and contracts with sites and vendors.
• Coordinate with ethics committees and competent authorities for approvals.

Precision for Medicine is a global Clinical Research Organization that combines novel clinical trial designs, operational and medical experts, advanced biomarker and data analytics, and a passion for rare diseases and oncology. The company values growth and innovation, fostering a collaborative and inclusive environment.

• Manage global, multi-center clinical research projects across therapeutic areas.
• Deliver projects on time, within budget, and to high quality standards.
• Lead and mentor multi-functional project teams and serve as the primary client contact.

PSI is a leading Contract Research Organization with 30 years of industry experience, offering a balance of stability and innovation to clients and employees. The company focuses on delivering quality, on-time services across therapeutic indications and invests in the professional development of its people.

• Own and maintain multiple program execution and partner pilot trackers, ensuring accurate milestones and status updates.
• Develop and distribute recurring biweekly program status reports consolidating information from multiple stakeholders.
• Coordinate partner working sessions, manage scheduling across time zones, and prepare meeting documentation.

Linda Werner & Associates is a staffing and recruiting firm that connects professionals with leading technology organizations. They offer a supportive culture with benefits including health insurance, paid time off, and retirement plans.