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Lead and oversee site budget and contract activities across assigned countries to ensure timely clinical trial start-up. Negotiate Clinical Trial Agreements (CTAs) and manage budgets while acting as an escalation point for complex discussions.
The Site SSU Lead is responsible for leading site activation teams and shaping study start-up strategies to ensure clinical trials are ready to enroll participants on time. This includes developing country-specific Informed Consent Forms and using data-driven insights to optimize performance and timelines.
Lead and oversee site budget and contract activities across assigned countries to ensure timely clinical trial start-up. Negotiate Clinical Trial Agreements (CTAs) and manage budgets while collaborating with study teams and sponsors.
Lead and support site activation teams to ensure clinical studies are activated efficiently and ready to enroll participants on time. Partner with Clinical Operations to improve timelines and develop country-specific Informed Consent Forms.
Manage study deliverables and site payment targets while ensuring adherence to quality standards and procedural documents. Act as the primary liaison for functional leads to resolve risks, issues, and contract modifications.
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Set the vision and strategic direction for the Specialty Testing business area, overseeing product development, clinical research, and compliance. Act as the medical representative to external partners and lead global strategies for health economics, policy, and reimbursement.
The specialist coordinates site start-up activities and manages essential regulatory documents for clinical trials. They serve as the primary contact for investigative sites and ensure compliance with ICH/GCP guidelines and sponsor specifications.
The Biostatistician II implements statistical analysis plans for complex longitudinal registry data in autoimmune disease areas. They compile, analyze, and report statistical data to support research projects, pharmacovigilance, and registry coordination.
The role focuses on driving the adoption of AI and emerging technologies to improve operational efficiency and business outcomes across all service lines. It involves leading cross-functional strategies, establishing AI governance, and partnering with leadership to implement innovative technology solutions.
The Clinical Specialist ensures the integrity of clinical trial data by reviewing assessment scales and providing guidance to raters. Responsibilities include conducting live interactions to improve scoring techniques and supporting rater performance through functional assessments.
The role is responsible for driving sustainable topline growth and profitability in Vietnam through the development and management of channel partners. Key duties include owning the market P&L, formulating go-to-market strategies, and managing relationships with key opinion leaders and internal stakeholders.
Oversee the strategy, implementation, and optimization of Workday HR technology solutions to enhance employee experience. Manage day-to-day HRIS operations, functional team leadership, and governance across HCM, Recruiting, Compensation, and Absence modules.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing clinical project teams, tracking study progress against milestones, and ensuring regulatory compliance and data integrity.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing project milestones, budgets, and ensuring protocol and GCP compliance while leading clinical team members.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves tracking study progress against milestones, managing resource allocation for CRAs, and ensuring regulatory compliance and data integrity.
The Senior CRA will oversee clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. Key tasks include conducting site visits, collaborating with cross-functional teams, and providing guidance to site staff and other CRAs.
The role focuses on completing investigator payment reconciliations in adherence to contractual guidelines and country regulations. Responsibilities include compiling patient activity data, managing bi-annual and final reconciliations, and resolving payment-related issues.
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The role involves conducting various site monitoring visits and delivering quality reports to ensure data integrity and patient safety. It also requires maintaining the Trial Master File and ensuring all site documentation complies with ICH/GCP guidelines.
The role involves monitoring investigator sites using a risk-based approach to ensure protocol compliance and data reliability. Responsibilities include conducting site visits, managing essential documentation, and maintaining collaborative relationships with investigative sites.
The CRA II is responsible for monitoring investigator sites to ensure protocol compliance, data reliability, and subject safety. This includes conducting remote and on-site visits, managing essential documentation, and maintaining collaborative relationships with clinical sites.
Serve as a scientific exchange resource for internal and external stakeholders by communicating balanced product and disease information. Lead the evidence strategy and dissemination process for the Shockwave Medical portfolio, including the creation of scientific content and KOL relationship management.
The Director of Clinical Research will co-own the strategy and execution of the clinical research program to support product validation and regulatory goals. This includes leading the design of observational and interventional studies and managing the clinical research infrastructure.
Lead the execution of pre- and post-market TAVI clinical studies by managing site relationships and providing procedural expertise during interventions. Collaborate with cross-functional teams to support product innovation and deliver educational programs to healthcare professionals.
Lead the drafting and management of complex clinical regulatory documents such as protocols, CSRs, and NDA modules. Act as the primary medical writing contact for clinical development programs and mentor junior writers.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. This includes conducting site visits, collaborating with cross-functional teams, and providing training to site staff.
The Medical Writer is responsible for authoring and delivering high-quality, regulatory-compliant clinical documentation such as protocols, CSRs, and investigator brochures. They will collaborate with cross-functional teams to ensure all deliverables meet project objectives and global regulatory standards.
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The Medical Writer is responsible for developing high-quality scientific content, including scientific platforms, lexicons, and materials for global conferences. The role involves collaborating with cross-functional teams to ensure all deliverables meet project objectives and regulatory requirements.
The Site Enablement Lead supports clinical study execution by identifying and training qualified research staff to accelerate study deliverables. They also optimize patient referral flows using the Referral Hub platform and manage site-level service agreements and staffing.
Design and execute evaluations for production LLM pipelines to ensure accuracy and quality in clinical data extraction. Build and maintain production-grade data models and a semantic layer to provide reliable business intelligence reporting across the organization.
The BDM is responsible for driving profitable growth within the Linguistic Validation business by developing strategic relationships with life sciences organizations. This includes managing the full sales cycle, from discovery and tailored solution development to commercial negotiation and revenue achievement.
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