The Medical Coding Specialist performs accurate and timely coding of clinical trial data, including adverse events and medical history, using MedDRA. They also collaborate with study teams to resolve coding queries and ensure data quality and consistency throughout the clinical development process.
The Senior Quality Manager provides functional and project-level quality oversight to ensure compliance with GCP and GxP regulations. They are responsible for managing vendor quality, overseeing CAPA processes, and conducting audits of systems and clinical trials.
The Senior Medical Director provides medical oversight and monitoring for oncology and hematology clinical trials while ensuring scientific credibility and regulatory compliance. They also partner with business development to support growth through bid strategy, proposals, and building relationships with key opinion leaders.
The Senior Director is responsible for developing business strategies, managing client relationships, and meeting annual sales goals within the DIID therapeutic area. They will coordinate RFI/RFP responses, lead bid defense meetings, and mentor junior business development staff.
The Drug Safety Officer manages local pharmacovigilance activities, including the collection, processing, and reporting of adverse events in compliance with regulatory requirements. They also collaborate with internal and external stakeholders to support safety documentation, audits, and process improvements.
The Senior Project Manager is responsible for managing multidisciplinary clinical study teams to ensure projects are delivered on time, within scope, and in compliance with regulatory requirements. They also manage project budgets, client relationships, and provide leadership and mentorship to project staff.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will provide unmasked support for ophthalmology studies, ensuring data integrity, subject safety, and protocol compliance.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with company SOPs and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data quality and protocol compliance throughout the study.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data quality and protocol compliance.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites while ensuring data integrity and subject safety. They will collaborate with study teams and sponsors to manage investigational products and maintain compliance with GCP and regulatory standards.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of study sites while ensuring adherence to GCP, ICH guidelines, and regulatory requirements. They will collaborate with study teams and sponsors to maintain data integrity and study blinding throughout the clinical development process.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will provide unmasked support, manage investigational product accountability, and ensure data integrity and protocol compliance throughout the study.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with SOPs and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data quality and protocol compliance throughout the study.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. They collaborate with study teams and sponsors to maintain protocol compliance and manage investigational product accountability.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with company policies and regulatory requirements. They will manage investigational product accountability, oversee unblinded site activities, and ensure data integrity and protocol compliance throughout the study.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with regulatory requirements and SOPs. They will ensure subject safety, data integrity, and protocol compliance while collaborating with study teams and sponsors.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. They will collaborate with study teams and sponsors to manage investigational products and maintain compliance with GCP and regulatory requirements.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. They will collaborate with study teams and sponsors to manage investigational products and maintain compliance with regulatory requirements and SOPs.
The role is responsible for developing and sustaining a consistent, scalable, and high-quality clinical database programming capability across the organization. Key tasks include managing improvement roadmaps, ensuring compliance and inspection readiness, and providing technical leadership for complex database programming issues.
The Proposals and Contracts Process Lead is responsible for developing and leading global proposals and contracts capability across Clinical Development Services. This role involves managing governance, process excellence, Salesforce/CRM expertise, and providing senior commercial support for strategic customer opportunities.
Lead end-to-end delivery of cross-functional clinical projects, ensuring adherence to timelines, budgets, and quality standards. Act as the primary point of contact for global pharmaceutical or biotechnology clients while managing multidisciplinary teams.
The Director of Business Development is responsible for developing sales strategies and managing client retention within the Oncology sector in Germany. This includes identifying new business opportunities, leading the RFP/RFI process, and coordinating bid defense meetings.
