Lead clinical data system projects from initiation to closeout, ensuring alignment of timelines and deliverables.
Serve as key contact for internal and external teams, facilitating communication and coordination.
Support business development activities and quality reviews to maintain high standards.
Our partner is a company that provides clinical trial data systems and services. They operate in an international, collaborative environment focused on clinical research and innovation.
Lead clinical data risk management and central monitoring across multiple clinical studies.
Evaluate clinical trial data to identify risks, trends, and emerging issues affecting study outcomes.
Develop key risk indicators and analytical approaches to support risk-based quality management.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. They operate globally but focus on efficient and fair candidate review processes.
Lead full-lifecycle clinical data management across all trials, ensuring data quality and integrity from eCRF builds to database locks and submission readiness.
Build and scale a high-performing Data Management organization, driving talent development and operational excellence.
Ensure strict compliance with global regulatory standards and manage CRO relationships to deliver high-quality results.
Kailera Therapeutics is a biotechnology company developing novel therapies for obesity and related conditions. The company fosters an entrepreneurial, team-oriented culture and is committed to creating an inclusive workplace.
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.
Create and maintain Study Trackers and monitor screening deadlines.
Review study visits and sweeps for readiness using page status and query reports.
Monitor review progress, identify issues and risks, and report to Lead Central Review Manager.
ICON is a global healthcare intelligence and clinical research organization that accelerates drug development. It is a large, values-driven organization with a focus on integrity, collaboration, agility, and inclusion.
Ensure operational efficiency and excellence in clinical data management services.
Manage team performance, budgeting, and process improvements.
Collaborate with stakeholders to optimize data management technology and standards.
Alimentiv is a clinical research organization specializing in data management services for clinical trials. The company has a global presence and emphasizes operational excellence, team leadership, and regulatory compliance.
Serve as primary contact for data management timelines, deliverables, and technical issues across clinical projects.
Oversee database design, UAT testing, data validation, and quality reviews to ensure compliance.
Train study teams, manage project resources, and support audits and bid defense meetings.
The company is a partner firm managing clinical data for life sciences research. They foster a collaborative, quality-focused culture and support professional development.
Lead clinical trial execution and operational delivery across internal and external stakeholders from start-up through execution.
Provide oversight of CROs, vendors, and clinical trial partners to ensure quality, compliance, timelines, and budget objectives are achieved.
Serve as the Clinical Operations leader for the team of CTMs, CRAs, and CTAs for each assigned project.
Immatics is a global leader in precision targeting of PRAME for cancer immunotherapy, with a robust clinical pipeline spanning TCR T-cell therapies and TCR bispecifics. The company fosters a collaborative and innovative culture focused on making a meaningful impact on patients.
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.
Independently manages significant aspects of clinical trials and research projects.
Trains and provides guidance to less experienced staff, and oversees data management.
Ensures compliance with regulations, monitors IRB submissions, and interfaces with study sponsors.
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate and prepare leaders for the future. The university is committed to diversity and inclusion, providing a supportive environment for staff and faculty.
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.
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.
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.
Build and scale clinical quality management programs and processes.
Coordinate day-to-day patient safety operations and incident review.
Collaborate with cross-functional teams to improve quality and safety of care.
InStride Health delivers specialty anxiety and OCD care for children and families. It is a growing organization that values heart, smart work, humility, and community.
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 execution of study-level activities, including creating trial documents and overseeing vendor delivery and budgets.
Coordinate country and regional trial management, aligning feasibility strategies and mitigating local risks.
Support program-level compound training and mentor new team members in Trial Management.
Johnson & Johnson is a global healthcare innovator focused on preventing, treating, and curing complex diseases through Innovative Medicine and MedTech. With a large workforce, they emphasize an inclusive work environment guided by their Credo, respecting diversity and dignity.
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.
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.
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.