The Director of Business Development is responsible for creating and executing sales strategies to meet annual goals and ensure client retention within assigned territories. They lead the proposal process, manage client relationships, and coordinate internal teams to respond to RFIs and RFPs effectively.
The Scientific Communications Project Manager will oversee the creation and review of scientific and medical assets in collaboration with internal and external stakeholders. They are responsible for managing tactical plans, tracking timelines, monitoring budgets, and developing process guidelines to ensure operational efficiency.
The Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with GCP and ICH guidelines. They ensure subject safety and data integrity by reviewing documentation, managing investigational products, and reporting findings through monitoring visit reports.
The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in accordance with GCP, ICH guidelines, and company SOPs. They ensure subject safety and data integrity while managing site documentation and reporting findings to project teams.
The Clinical Database Programming Process Lead is responsible for the strategy, development, and governance of high-quality clinical database programming capabilities across the organization. This role involves providing senior technical leadership, managing process improvements, and ensuring compliance with global standards and inspection readiness.
The Project Manager will plan and manage multidisciplinary study teams to ensure clinical trials are delivered on time, within scope, and within budget. They are responsible for maintaining client relationships, managing project risks, and ensuring compliance with quality standards.
The Director of Business Development is responsible for driving sales strategies, identifying new business opportunities, and managing client relationships within the Internal Medicine and Neuroscience sector. They will coordinate proposal processes, lead bid defense meetings, and monitor competitor activities to ensure company growth.
The Manager, Vendor Management will lead governance, oversight, and performance management activities for an assigned vendor portfolio. They are responsible for ensuring vendor quality, compliance, and cost optimization while managing the full vendor lifecycle.
The Clinical Research Associate is responsible for supporting clinical development projects and ensuring that customer goals are achieved. They work alongside innovative professionals to deliver tailored clinical research services across various therapeutic areas.
The Clinical Research Associate is responsible for the initiation, monitoring, and close-out of clinical study sites in compliance with SOPs, GCP, and ICH guidelines. They ensure subject safety and data integrity by reviewing documentation and managing investigational products.
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 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 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.
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.
