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The coordinator manages the negotiation of confidentiality disclosure agreements and oversees the execution of site-level clinical trial agreements. They serve as the primary point of contact for investigative sites and vendors while ensuring all documentation meets quality and regulatory standards.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. You will provide feedback on methodology and scoring while maintaining accurate documentation for all assigned tasks.
The Clinical Territory Associate will provide technical and clinical support to surgical teams while training to become an expert in da Vinci surgical systems. They will also lead product demonstrations and contribute to regional sales goals through customer engagement and administrative reporting.
The Clinical Territory Associate will provide technical and clinical support to surgical teams while training to become an expert in da Vinci surgical systems. The role involves leading product demonstrations, managing customer relationships, and contributing to regional sales goals.
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.
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The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor-dedicated studies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical expertise to project teams throughout the clinical trial lifecycle.
Lead day-to-day clinical trial operations from start-up through close-out while managing study timelines and enrolment targets. Provide oversight of CRA activities, ensure protocol compliance, and manage relationships with sponsors and investigators.
The Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining high-quality study documentation. They will also manage site relationships, support patient recruitment, and validate study data throughout the clinical trial lifecycle.
The Clinical Trial Manager is responsible for leading and coordinating project activities to ensure delivery on time, within budget, and to high quality standards. Key tasks include managing project plans, leading cross-functional teams, and monitoring progress to mitigate risks.
You will own the delivery and people management for the engineering group, ensuring sprint predictability and high-quality software standards. You will also partner closely with product managers to align technical execution with strategic business goals.
The Senior Platform Engineer will own developer experience and application frameworks while bridging the gap between DevOps and data engineering. They will also build automation for data quality checks and mentor the engineering team through code and design reviews.
You will provide critical diagnostic information for veterinary patients while receiving mentorship and feedback from experienced radiologists. The role involves reading both known and live cases to prepare for board certification and maintain high reporting standards.
The Senior Clinical Research Associate will conduct countrywide monitoring visits to ensure data integrity and patient safety at investigator sites. They are responsible for maintaining Trial Master Files and delivering quality monitoring reports in accordance with clinical monitoring plans.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, conduct site visits, and manage essential documentation to guarantee data reliability and subject well-being.
The Medical Information Specialist is responsible for acquiring, organizing, and disseminating critical medical information to support healthcare professionals. This role involves staying updated on pharmaceutical advancements, clinical trials, and breakthrough therapies to provide accurate medical data.
Provide patient support through calls and emails regarding diabetes treatment technologies. Build meaningful relationships with customers while meeting quality and productivity targets.
Manage the performance and workload of medical writers while overseeing the preparation and quality of publication deliverables. Lead resource planning, budget preparation, and the development of departmental training programs and SOPs.
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The Clinical Territory Associate provides technical and clinical guidance to surgical teams on the use of the da Vinci Surgical System. The role evolves from a technical focus in the first year to include sales activities and program development in the second year.
Translate and edit content from English to Portuguese specifically within the logistics and supply chain niche. Ensure text readability, clarity, and grammatical accuracy while comparing translations against source files.
Serve as the senior scientific authority for Clinical Outcome Assessment (COA) and Patient Experience Data (PED) strategies for pharmaceutical and biotechnology clients. Lead the scientific quality of deliverables, mentor multidisciplinary teams, and represent the company as an external thought leader in COA science.
Provide high-quality mental health support through psychotherapy, counseling, or coaching sessions. Lead support groups and deliver Masterclasses to users across the Asia-Pacific and Europe regions.
Lead the full cycle of Clinical Data Management for oncology studies, serving as the primary point of contact for sponsors. Responsibilities include creating eCRFs, cleaning data, and managing vendor contracts and budgets.
Provide medical leadership and support for clinical trials, including the creation of protocols and real-time medical monitoring of study subjects. Serve as the primary medical liaison between the sponsor and internal departments to ensure study compliance and safety.
Provide scientific support for RWE/Epidemiology studies through literature reviews, data cleaning, and the development of scientific deliverables. Coordinate operational activities and oversee vendor deliverables to ensure high-quality study execution.
Respond to customer queries via phone and written channels regarding Nestlé product nutrition and dietary restrictions. Provide counseling on food intake and collaborate with stakeholders to support business decision-making based on health and nutrition topics.
The role involves providing technical expertise, training, and software demonstrations of medical imaging solutions to clients via webinars and on-site visits. Additionally, the specialist acts as a liaison between clients and the development team to provide feedback for product enhancements.
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Provide strategic medical and scientific expertise in hematology-oncology to support proposal development, protocol design, and clinical development plans. Act as a subject matter expert and consultant throughout the research and development lifecycle to guide project teams and sponsors.
Support the growth and engagement of the Brazilian nutritionist network and provide clinical expertise to improve the Nutrium software. Responsibilities include organizing webinars, onboarding providers, and creating nutrition education content for patients.
Design and implement statistical strategies and analysis plans for clinical trials across various therapeutic areas. Perform SAS programming to generate study reports and provide expert guidance on methodology and sample size calculations.
The Senior Clinical Data Manager provides leadership for assigned projects, ensuring global accountability and effective management of CDM deliverables. They oversee vendor performance, manage budgets, and ensure data quality compliance across complex clinical trial programs.
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