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• Lead and manage a team of Project Directors and Project Managers for global clinical trials.
• Oversee project delivery, sponsor interactions, and profitability across clinical programs.
• Ensure compliance with GCP/ICH and drive continuous improvement and KPIs.

Precision Medicine Group is a precision medicine company providing clinical research and development services. They emphasize quality, people, clients, and performance, with a collaborative team environment.

• Manage global, multi-center clinical research projects in a variety of therapeutic areas.
• Deliver projects on time, within budget, and in accordance with high quality standards.
• Lead and mentor project teams, and serve as the primary point of contact to clients on all project matters.

PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. They focus on delivering quality and on-time services across a variety of therapeutic indications.

• Manage global, multi-center clinical research projects in various therapeutic areas.
• Deliver projects on time, within budget, and to high quality standards while leading multifunctional teams.
• Serve as primary client contact, participate in bid defenses, and ensure compliance with procedures.

PSI is a leading Contract Research Organization with 30 years of experience in the industry, offering a balance between stability and innovation. We focus on delivering quality and timely services across various therapeutic indications, investing in our people's professional development.

• Oversee study start-up, site activation, and close-out activities while managing study plans and essential documents.
• Collaborate with cross-functional teams, sponsors, and vendors to ensure timely and compliant project execution.
• Mentor CTA team members and contribute to TMF quality, inspection readiness, and regulatory compliance.

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. They are a collaborative community committed to making a meaningful impact on global health, valuing team members and empowering them.

• Develop study budgets for bids and change orders, and manage budgets throughout clinical project duration.
• Manage sponsor contracts, payment schedules, and timesheet systems.
• Provide financial analysis and reporting for clinical projects.

PSI is a leading Contract Research Organization with more than 25 years on the market, offering a perfect balance between stability and innovation. They focus on delivering quality and on-time services across a variety of therapeutic indications.

• Take your career to the next level and lead challenging global clinical research projects.
• Manage the full scope of responsibilities and get hands-on involvement in every aspect of the study.
• Work remotely or hybrid while managing multi-functional project teams and client relationships.

PSI is a leading Contract Research Organization with 30 years of experience, offering a balance between stability and innovation. They focus on delivering quality and on-time services across various therapeutic indications, and invest in their people's professional development.

• Oversee clinical study operations from startup through close-out, ensuring quality and compliance.
• Act as primary operational partner to sponsors, project teams, and clinical sites.
• Foster a culture of quality by coaching peers on GCP compliance and documentation discipline.

Beacon Biosignals is transforming precision medicine for the brain, offering EEG and cardiopulmonary platforms for clinical development and diagnostics. The company has office hubs in Boston, New York, and Paris, and fosters a first-class remote work culture with a focus on diversity and impact.

• We oversee a team of Clinical Research Project Managers delivering clinical studies and observational research programs.
• We shape team performance, resource strategy, operational excellence, and talent development across a diverse project portfolio.
• We ensure delivery against scope, timelines, budgets, quality standards, client expectations, and business objectives.

Jobgether uses AI-powered matching to connect candidates with hiring companies. This position is listed on behalf of a partner company that manages all applications, and the role is within a clinical research organization focused on delivering clinical studies and observational research programs.

• Manage day-to-day clinical trial operations, including CRO/vendor oversight and site management.
• Lead cross-functional study teams, develop study documents, and implement risk mitigation strategies.
• Ensure high-quality deliverables within timelines and budget, from start-up through close-out.

Ultragenyx is a biopharmaceutical company dedicated to developing life-changing treatments for rare diseases. They foster a supportive and inclusive culture focused on learning and growth, with a global team committed to innovation.

• Oversee all aspects of planning and execution of client patient adherence and medical education projects.
• Communicate with clients and leadership, maintain client relationships, and drive implementation strategies.
• Develop project schedules, conduct data analysis, manage vendors, and lead internal and external status meetings.

Momentum Life Sciences helps the healthcare industry connect, motivate, and empower people to engage in their health. With more than 30 years of experience, they are a leading provider of patient and healthcare professional engagement solutions.

• Oversee day-to-day operations of clinical trials, ensuring compliance with GCP, FDA, and ICH guidelines while managing CROs and vendors.
• Serve as primary point of contact for CROs and trial vendors, tracking performance metrics, budgets, and timelines to ensure project success.
• Collaborate with cross-functional teams to prioritize data integrity, participant safety, and quality control, with travel required up to 30%.

Peptilogics is a surgical therapeutics company dedicated to curing and preventing medical device-related infections. They are a clinical-stage biotech with a small, agile team and a culture of proactive, independent thinking.

• Lead interdisciplinary oncology clinical research projects from study launch through closeout, ensuring quality, timelines, budgets, and compliance.
• Serve as the primary liaison between the organization and the sponsor, overseeing project deliverables, risk management, and financial performance.
• Maintain accountability for study documentation, inspection readiness, and accurate information across relevant databases and systems.

Jobgether uses AI to match job seekers with roles. They are a platform that partners with hiring companies to manage applications and next steps.

• Collaborate with project teams and clinical sites to support study startup, training, and device deployment.
• Ensure compliance with GCP, ICH guidelines, and regulatory standards while monitoring project progress.
• Address operational issues and provide feedback to improve devices and workflows.

Beacon Biosignals is transforming precision medicine for the brain by offering at-home EEG platforms for clinical development and diagnostics. The company fosters a remote-first culture with office hubs in Boston, New York, and Paris, emphasizing asynchronous work and collaboration.

• Oversee strategic planning and execution of global clinical studies.
• Manage internal and external resources, including CROs, to ensure quality and compliance.
• Lead cross-functional teams and contribute to trial design and budgeting.

Dianthus Therapeutics is a clinical-stage biotechnology company developing novel therapies for severe autoimmune diseases. The company values a culture centered on core principles and aims to elevate patient care.

• Serve as the primary point of contact for assigned protocols, linking Country Operations with the clinical trial team.
• Manage project timelines, deliverables, and performance for clinical studies from feasibility to close out.
• Ensure compliance with ICH/GCP, country regulations, and company policies while leading local study teams.

Merck is a global healthcare leader with a diverse range of prescription medicines, vaccines, and animal health products. With over 100 years of history, the company employs tens of thousands worldwide and fosters a culture of innovation and inclusivity.

• Oversee regional project management, ensuring high-quality delivery and compliance with global standards.
• Manage financial aspects including project margin, profitability, and reporting.
• Lead and develop project management team, including training and line management.

Brandtech+ is a global creative production company specializing in film, CGI, automation, AI, motion design, and digital/print content. They partner with over 300 clients in 40+ countries and are part of The Brandtech Group, focusing on innovation and high-quality solutions.

• Support operational execution of clinical studies from initial synopsis through final deliverables.
• Manage implementation, on-time execution, and conduct of clinical studies, including budget and vendor management.
• Oversee cross-functional study teams and ensure compliance with regulations and data integrity.

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. They are committed to continuous innovation in cell therapy.

• Manage clinical study vendors and ensure deliverables are on time, within budget, and compliant with FDA and ICH/GCP guidelines.
• Support CRO collaboration, site start-up, study documentation, and risk mitigation with cross-functional teams.
• Leverage AI tools and process improvements to enhance clinical operations productivity and quality.

This biotechnology company focuses on developing innovative oncology therapies. It offers a collaborative, multidisciplinary environment with opportunities to use AI-enabled tools and modern approaches to clinical operations.

• Lead and oversee global clinical trials from inception to closure, managing cross-functional teams and vendors.
• Ensure compliance with ICH/GCP and regulatory standards while driving recruitment and risk management strategies.
• Manage study materials, systems (EDC, IRT, CTMS), and provide training to stakeholders.

AbbVie is a biopharmaceutical company focused on discovering and delivering innovative medicines in immunology, oncology, neuroscience, and aesthetics. With a global presence, they emphasize integrity, innovation, and community service.

• Manage multiple medical communications publications projects throughout the project lifecycle.
• Develop and maintain project plans, timelines, budgets, and status reports.
• Coordinate cross-functional teams and serve as a key point of contact for clients and internal teams.

ApotheCom is a leader in medical communications, providing high-quality programs for pharmaceutical clients. They are a collaborative team with a focus on diversity and inclusion, offering a supportive environment.