The Senior Clinical Trial Manager oversees clinical investigative sites and clinical monitoring deliverables to ensure study quality and adherence to timelines. They are responsible for mentoring Clinical Research Associates, identifying site performance issues, and implementing corrective action plans.
The Risk Manager develops and executes risk-based monitoring strategies to ensure data integrity and quality throughout the clinical trial lifecycle. They collaborate with cross-functional teams to identify, assess, and mitigate project risks while providing strategic guidance and training to study teams.
The Clinical Data Coordinator supports clinical data management activities to ensure accurate, secure, and compliant data collection for clinical trials. Responsibilities include data review, reconciliation, discrepancy management, and assisting with database design and documentation maintenance.
The Risk Manager is responsible for developing and executing risk-based monitoring strategies to ensure data quality and integrity throughout the clinical trial lifecycle. They collaborate with cross-functional teams to identify, assess, and mitigate risks while providing strategic input and training to study teams.
The Manager, Project Coordination provides leadership and oversight to project teams, ensuring adherence to processes, workflows, and project timelines. They are responsible for hiring, mentoring, and managing the performance of staff while identifying process improvements and maintaining quality standards.
The central monitor conducts holistic statistical reviews of clinical study data to identify risks and ensure data quality throughout the study lifecycle. They are responsible for proactive identification, escalation, and management of risks at the study, country, and site levels.
The Senior Statistical Programmer will lead clinical trials, developing and validating SDTM and ADaM datasets, TLFs, and submission packages. They will also collaborate with biostatistical teams to ensure deliverables meet regulatory standards and internal SOPs.
The Site Budget and Contract Lead manages the development, negotiation, and execution of investigator budgets and clinical trial agreements across global study sites. They act as the primary point of contact for sponsors and internal teams to ensure study budgets remain within scope and timelines.
The Site Budget and Contract Lead manages the development, negotiation, and execution of investigator budgets and clinical trial agreements across global studies. They act as the primary point of contact for sponsors and sites, ensuring all activities remain within scope and compliant with internal processes.
Lead assigned clinical trials from initiation through closeout, coordinating study teams, vendors, budgets, timelines, and deliverables while ensuring compliance with applicable regulations and quality standards. Serve as the primary sponsor contact, oversee study start-up and execution, manage risks and recruitment progress, and keep studies audit-ready.
The Senior CRA conducts site qualification, initiation, monitoring, and close-out visits in accordance with protocols and regulatory guidelines. They also build productive relationships with site staff and ensure accurate data collection and regulatory document maintenance.
The central monitor conducts holistic statistical reviews of clinical study data to identify risks and ensure data integrity from start to database lock. They proactively communicate and manage risks at the study, country, and site levels while following established clinical trial procedures.
The Site Budget and Contract Lead manages the development, negotiation, and execution of investigator budgets and clinical trial agreements across global sites. They act as the primary point of contact for sponsors and internal teams to ensure study timelines and budget scopes are maintained.
The Site Budget and Contract Lead manages the development, negotiation, and execution of investigator budgets and clinical trial agreements across global study sites. They act as the primary point of contact for sponsors and internal teams to ensure all contracting activities remain within scope and adhere to study timelines.
The Accounting Clerk will support daily financial operations for the Argentina entity, including bank reconciliations, vendor payments, and tax management. They will also coordinate with external accounting firms and auditors to ensure accurate, compliant financial reporting.
The Project Manager oversees the initiation, planning, and execution of clinical research projects while ensuring compliance with budgets, timelines, and regulatory standards. They act as a primary contact for stakeholders and coordinate tasks across various departments to ensure successful site activation and study delivery.
The Associate Director provides senior leadership and line management oversight for the Project Management function to ensure high-quality project delivery. They act as a strategic partner to senior leadership, driving operational excellence, resource planning, and the development of high-performing teams.
The Clinical Data Coordinator supports clinical data management activities to ensure data accuracy, security, and regulatory compliance. Responsibilities include data review, reconciliation, discrepancy management, and assisting with study documentation and database design.
The Senior Director is responsible for managing sales activities, key accounts, and business development strategies within the China territory. They will also represent the company at industry events and collaborate with management to define revenue growth strategies.
The Director of Vendor Management leads the enterprise vendor governance program, overseeing vendor qualification, performance, risk, and strategic partnerships. They collaborate cross-functionally to ensure vendor services support clinical trial delivery while managing VMO resources and budgets.
The Clinical Trial Delivery Trainer develops, maintains, and delivers training programs for clinical trial staff to ensure operational readiness and regulatory compliance. They also provide coaching, facilitate knowledge sharing, and collaborate with leadership to improve training effectiveness and organizational processes.
The Clinical Data Coordinator supports clinical data management activities to ensure data is collected, managed, and reported accurately and securely. Responsibilities include data review, reconciliation, discrepancy management, and assisting with study documentation and database design.
The Principal Central Monitor leads the development of tools and analyses for centralized statistical review to proactively identify and manage study risks. They act as a strategic lead across multiple studies, mentoring junior staff and ensuring monitoring approaches align with study data and processes.
Lead complex, high-risk validation initiatives across the lifecycle of GxP computerized systems, including strategy, risk assessment, documentation, execution, and release or retirement. Provide technical oversight, coordinate project schedules and stakeholders, mentor analysts, and support audits, inspections, and continuous improvement of CSV practices.
The Vice President of Medical Affairs will provide unified leadership for Medical Monitoring and Pharmacovigilance functions, overseeing strategy, P&L, and regulatory compliance. The role involves driving business development, managing client relationships, and advising the Chief Medical & Scientific Officer on medical and safety risks.
The Medical Monitor provides medical and scientific support to clinical research programs, ensuring data integrity and subject safety oversight. They act as the primary medical contact for investigators and project teams, managing safety reporting and protocol-related medical inquiries.
The Senior Statistical Programmer will lead clinical trials by developing and validating SDTM and ADaM datasets, TLFs, and submission packages. They will also collaborate with biostatistical teams to ensure deliverables meet regulatory standards and internal SOPs.
The Senior Statistical Programmer will lead clinical trials by developing and validating SDTM and ADaM datasets, TLFs, and submission packages. They will also collaborate with biostatistical teams to ensure deliverables meet quality standards and regulatory requirements.
The Senior Project Manager serves as the primary point of contact for sponsors, overseeing all phases of clinical trials from start-up to closure. They are responsible for managing project budgets, timelines, vendor deliverables, and leading cross-functional teams to ensure studies are audit-ready.
The Talent Acquisition Advisor manages the full-cycle recruitment process and acts as a business partner to hiring managers to identify and attract top talent. They are responsible for developing sourcing strategies, maintaining recruitment systems, and supporting employer branding initiatives.
