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• 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.

• Serve as primary point-of-contact and escalation point for clients, coordinating functional services and vendors to meet quality, scope, cost, and time objectives.
• Manage study budget and financial health, ensuring projects remain within scope and identifying out-of-scope activities, while overseeing billing and forecasting.
• Develop robust project plans with timelines and risk management, ensure quality management including eTMF inspection readiness, and lead internal and client meetings.

Precision for Medicine is a CRO that integrates clinical trial execution with scientific expertise and data sciences to accelerate life-changing therapies, focusing on Oncology and Rare Disease. It is a growing organization that values employee contributions and fosters a collaborative culture.

• 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.

• 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.

• 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.

• Build and maintain excellent client relations to ensure high-quality service.
• Work closely with internal teams and third-party partners to support clinical trial materials projects.
• Assist in financial management and produce regular status updates for clients.

MEDiSTRAVA is a leader in medical communications, providing targeted solutions across strategy, patient engagement, and clinical trial optimization. They have a dynamic team and offer a friendly, informal working environment with growth opportunities.

• 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 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.

• Manage end-to-end clinical studies ensuring on-time and on-budget delivery with high quality standards.
• Lead multifunctional study management teams and serve as primary point of contact for client study teams.
• Oversee project planning, resource allocation, and financial management while ensuring regulatory compliance.

Science 37 is a clinical research organization focused on decentralized clinical trials. They value employee well-being and provide an equal opportunity workplace.

• 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.

• Manage projects from brief to delivery, ensuring timelines, budgets, and quality standards are met.
• Build trusted client relationships and coordinate cross-functional teams for seamless project delivery.
• Manage project finances including estimates, tracking, reconciliation, and forecasting.

Nucleus Global is a global leader in medical communications with locations across Europe, US, and APAC, serving over 90 clients. It is part of the Inizio Medical group, which includes three top medical communications companies, offering unmatched scale and expertise.

• 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.

• 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.

• 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.

• Serve as the primary clinical point of contact for clients and lead the operational conduct of clinical studies.
• Develop study-related clinical documents, train CRAs, and drive site feasibility and recruitment strategies.
• Oversee study submissions, monitoring, data quality, and vendor management, ensuring compliance with GCP and regulatory requirements.

Precision for Medicine is a CRO that integrates clinical trial execution with scientific expertise and advanced data sciences, focusing on Oncology and Rare Disease. They leverage new technologies and operational scale to improve the speed and cost of bringing therapies to patients.

• Responsible for executing one or more elements of clinical studies in compliance with quality standards and regulations.
• Supports the Study Project Manager in leading cross-functional study teams and developing study protocols.
• Manages vendor selection, oversight, and study-related training, and proactively resolves issues.

AbbVie is a biopharmaceutical company focused on discovering and delivering innovative medicines and solutions for serious health issues. It is a large global organization with a diverse workforce and a commitment to integrity and innovation.

• 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.

• Lead end-to-end clinical data review activities across complex trials, ensuring data accuracy and quality for analysis.
• Serve as primary contact for internal and external stakeholders, managing timelines, budgets, and resources.
• Mentor junior team members and provide subject matter expertise in clinical data science and analytics.

• Oversee global clinical trial execution, including site selection, activation, enrollment, and closeout, while ensuring compliance with GCP and regulatory requirements.
• Partner with CROs to drive robust trial management, data monitoring, and patient enrollment strategies, and review study-related plans and documents.
• Mentor and guide clinical operations team members, track performance metrics, and ensure inspection readiness across all study phases.

Summit Therapeutics is a biopharmaceutical oncology company focused on improving quality of life and resolving unmet medical needs through innovative clinical studies. With multiple global Phase 3 trials and offices across the US, UK, and Ireland, the company is committed to a collaborative, people-driven culture.

• Leads and oversees global clinical trials from inception through closure, ensuring quality and efficiency.
• Manages external vendors, recruitment strategies, and cross-functional team coordination.
• Maintains inspection readiness and contributes to risk management and process improvement.

AbbVie discovers and delivers innovative medicines and solutions for serious health issues across immunology, oncology, and neuroscience. The company is a global biopharmaceutical leader with a focus on making a remarkable impact.