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The Clinical Success Manager will demo, install, and train clinics on automation software while proactively managing customer relationships and feedback. They will also collaborate with the sales team to support prospective customers and develop training materials to improve clinical efficiency.
The Workforce Coordinator is responsible for managing staffing schedules, resource allocation, and monitoring real-time workforce activity to ensure operational efficiency. They will collaborate with stakeholders to analyze performance metrics, identify staffing gaps, and provide actionable insights to management.
Execute manual and automated tests to validate application functionality and ensure high quality standards. Collaborate with cross-functional teams to identify, document, and resolve software defects throughout the development lifecycle.
The role provides scientific support for epidemiology studies by conducting literature reviews, data cleaning, and quality control activities. It also involves coordinating operational tasks across multiple studies to ensure high-quality execution and cross-functional alignment.
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.
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The Personal Assistant will manage calendars, communications, and travel arrangements while providing comprehensive administrative support to an executive. They are responsible for organizing documents, tracking expenses, and ensuring all professional and personal commitments are handled efficiently.
The Clinical Research Associate will conduct onsite monitoring visits, manage site communications, and ensure data quality and compliance with study protocols. They will also support study startup activities, regulatory submissions, and oversee project timelines and schedules.
The Senior Clinical Research Associate will conduct monitoring visits at investigator sites to ensure data integrity and patient safety in accordance with clinical monitoring plans. They are responsible for maintaining the Trial Master File and ensuring all site documentation is accurate and compliant with ICH/GCP guidelines.
The Operations Assistant will provide administrative and operational support to managers and internal teams to ensure daily business activities run smoothly. Responsibilities include coordinating workflows, maintaining operational documentation, managing schedules, and tracking key business metrics.
Respond to customer queries regarding pet nutrition, health, and behavior through phone and written channels. Maintain accurate records, handle consumer complaints, and build relationships with market stakeholders to support business decisions.
The Senior Manager will lead global Medical Affairs strategies, fostering partnerships with Key Opinion Leaders and managing scientific evidence generation. They will also provide medical leadership throughout the product lifecycle and ensure all communications comply with regulatory and ethical standards.
The Scheduling Coordinator will manage calendars, appointments, and meetings while ensuring efficient coordination across various stakeholders. Responsibilities include tracking scheduling changes, maintaining CRM data, and preparing reports to ensure service standards are met.
The Administrative Coordinator will manage daily operations, including calendar scheduling, document organization, and communication between internal and external teams. They are also responsible for preparing reports, tracking expenses, and identifying process improvements to enhance administrative efficiency.
The Project Assistant provides administrative and operational support to project teams throughout the project lifecycle. Responsibilities include tracking project milestones, scheduling meetings, maintaining documentation, and ensuring tasks are completed on time.
This role provides scientific and strategic leadership for real-world evidence and epidemiology studies, serving as the primary lead for assigned scientific workstreams. The incumbent ensures scientific rigor, operational feasibility, and quality across study protocols, publications, and analytical deliverables.
The Telesales Representative will generate sales through outbound and inbound calls while maintaining accurate records in the CRM. They are responsible for identifying customer needs, overcoming objections, and meeting or exceeding established sales targets.
The Medical Director will provide expert medical guidance to project teams and ensure clinical studies adhere to ethical and legal standards. They will also oversee safety data reviews, contribute to study documentation, and support business development efforts.
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The Administrative Specialist will provide comprehensive operational support by managing documentation, databases, and internal communications. They are responsible for maintaining accurate records, coordinating schedules, and ensuring administrative processes are followed efficiently.
The role involves administering, scoring, and reviewing psychiatric assessments such as MINI and MADRS for a depression study. You will act as a Central Independent Rater to support clinical trial data integrity.
The Clinical Education Representative will deliver high-quality training programs to healthcare professionals regarding Essity's healthcare solutions. They will also manage customer relationships, identify learning needs, and contribute to account development to improve patient outcomes.
The Document Processing Specialist is responsible for managing, verifying, and maintaining documents across internal systems to ensure accuracy and efficiency. They will perform data entry, conduct quality checks, and coordinate with internal teams to resolve document-related issues.
The Senior Medical Science Liaison acts as a field-based medical representative to build relationships with healthcare professionals and key opinion leaders. They are responsible for exchanging scientific information, collecting medical insights, and supporting clinical trial activities within their assigned territory.
The Senior Clinical Research Associate acts as a subject matter expert, providing mentorship and performance feedback while overseeing site monitoring and study integrity. They manage monitoring services for complex projects, ensure adherence to SOPs, and facilitate effective communication between site staff and sponsors.
The Medical Director provides medical leadership for clinical trials, including protocol development, medical monitoring, and safety evaluation. They serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and effective issue resolution.
The Appointment Setter will connect with potential customers to qualify leads and schedule meetings for the sales team. They are responsible for maintaining CRM records, managing calendars, and meeting consistent performance targets.
The Senior Decentralized Clinical Trial Study Lead is responsible for the strategic development and delivery of decentralized clinical trials, ensuring they meet quality, speed, and financial objectives. They act as the primary point of contact for customers and lead cross-functional teams to manage study milestones, risks, and project performance.
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The Senior Clinical Pharmacologist will lead clinical pharmacology strategies across early and late-phase drug development programs while partnering with cross-functional teams to drive decision-making. They will apply model-informed drug development principles to support dose selection, biomarker optimization, and regulatory submissions.
Provide expert clinical and technical support for the Farapulse system during medical procedures and educate hospital staff on its safe usage. Manage client relationships and identify clinical needs while traveling across the assigned territory to meet business goals.
The incumbent will lead medical science and strategy for metabolic clinical research, providing expert input on development plans, regulatory issues, and clinical trial protocols. They will also engage in business development, support client proposals, and mentor internal clinical teams to ensure high-quality delivery of research projects.
The incumbent will lead medical science and strategy for oncology, driving business outcomes through proposal development, client engagement, and strategic clinical trial design. They will also provide therapeutic expertise to internal teams, mentor clinical scientists, and contribute to innovative clinical research initiatives.
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