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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 Clinical Operations Manager oversees a team of clinical staff, ensuring monitoring activities meet sponsor requirements and quality standards. They are responsible for resource allocation, performance management, and driving process improvements through innovation and technology adoption.
The Clinical Territory Associate will provide technical and clinical support to surgical teams while training to become an expert in da Vinci robotic surgery. They will also contribute to sales goals by leading product demonstrations, in-services, and managing regional sales activities.
The Clinical/Medical Scientist will develop medical plans and perform regular medical data reviews to identify risks and trends in infectious disease studies. They will also serve as a primary interface between internal teams, customers, and vendors to ensure project milestones and quality deliverables are met.
The associate will track rater experience qualification data and coordinate logistical matters for investigator meetings. They are also responsible for managing scale licenses, translations, and ensuring adherence to rater training and data surveillance plans.
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Conduct health surveys to collect data on patient well-being, medical history, and risk factors. Ensure accurate transcription of health information and assist patients with understanding their medical backgrounds.
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.
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.
The Senior Clinical Data Manager will oversee the end-to-end data management process for clinical trials, ensuring accuracy, security, and compliance with protocols. Responsibilities include database setup, data cleaning, vendor oversight, and providing regular status reports to clients and project teams.
Perform site monitoring visits to ensure compliance with regulatory requirements and Good Clinical Practice guidelines. Manage study progress by tracking regulatory submissions, subject recruitment, and data integrity across assigned clinical sites.
The Senior Clinical Research Associate II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and act as a primary liaison to ensure project objectives and timelines are met.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and regulatory standards. Additionally, you will coordinate study setup activities including investigator identification, regulatory submissions, and site initiation visits.
The Clinical Scientist collaborates with the Medical Director to develop medical plans and perform regular reviews of clinical data to identify trends and safety risks. They serve as the primary interface between internal teams and customers to ensure project milestones and quality deliverables are met.
The Clinical/Medical Scientist will collaborate with the Medical Director to develop medical plans and perform regular medical data reviews to ensure subject safety and data integrity. They will also serve as a primary interface between internal teams, customers, and vendors to manage project deliverables and timelines.
Provide medical advice and guidance to patients through telematics such as phone, video, or chat. Assess clinical severity, prescribe medication when necessary, and coordinate emergency medical resources.
The Associate Manager is responsible for interviewing, selecting, and onboarding CRA/IHCRA candidates while ensuring they are properly trained and mentored. They also manage performance, review quality metrics, and act as a point of escalation for project-related issues.
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The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects and caregivers. They will also provide central monitoring by reviewing neuropsychological test data to ensure accuracy and provide feedback to other raters.
You will oversee clinical trial management workstreams, ensuring all deliverables meet quality, timeline, and regulatory standards. This includes collaborating with cross-functional teams to implement protocols, manage budgets, and optimize study outcomes through data analysis.
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.
The Senior Clinical Trial Manager is responsible for executing clinical studies in compliance with quality standards and global regulations. They support the study project manager in leading cross-functional teams, managing external vendors, and ensuring study documentation and systems are up to date.
The role involves leading clinical trial start-up activities, including site activation and the preparation of essential regulatory documents. You will collaborate with cross-functional teams to streamline processes and provide guidance to study teams to ensure compliance and project success.
The Clinical/Medical Scientist supports the Medical Director in developing medical plans and performing regular medical data reviews to identify risks and trends. They serve as the primary interface between internal teams, customers, and vendors to ensure project milestones and data integrity are maintained.
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, manage customer in-services, and contribute to regional sales goals.
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.
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The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. The consultant will also provide feedback on methodology and scoring while maintaining accurate documentation for all assigned tasks.
Perform manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles involve clinical decision-making regarding site performance and overseeing targeted site interventions.
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 administrative tasks, and contributing to regional sales goals.
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