The role involves directly administering assessments to clinical trial participants or evaluating the quality of assessments performed by others, providing feedback on interview technique and scoring to ensure data reliability. Responsibilities also include evaluating case data, conducting live interactions with raters for guidance, and completing all assigned tasks and documentation timely.
Remote Clinical Research Jobs (612)
Tags = clinical-research
The Senior Manager, Clinical Partner Outsourcing ensures seamless execution of clinical studies by developing robust supplier contracts through commercial negotiations and resolving commercial and operational challenges. This role is responsible for maintaining fiscal discipline, enhancing cross-functional collaboration, and ensuring studies start on time aligned with business requirements and Takeda standards.
The role involves conducting comprehensive nutritional assessments and providing ongoing counseling and motivational support to participants in international clinical studies focused on metabolic diseases. Responsibilities also include monitoring participant progress and collaborating with the clinical research team to ensure adherence to study protocols.
Associate Director, Clinical Trial Management
NewAmsterdam Pharma Corporation
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Full Time
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21 Weeks Ago
NewAmsterdam Pharma Corporation
This role supports the planning, initiation, execution, and closeout of clinical trials, ensuring compliance with regulatory standards, timelines, and budget while maintaining patient safety. Key duties involve coordinating operational activities, managing vendors like CROs, and ensuring high-quality data collection and reporting.
Head of R&D and Scientific Strategy, Rare Disease
Syneos Health
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Full Time
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22 Weeks Ago
Syneos Health
The Head of R&D and Scientific Strategy supports or leads matrix teams to drive value by leveraging scientific capabilities, often focusing on cross-functional initiatives and developing innovative solutions for customers under the CSO's guidance. This role involves contributing to scientific communications, engaging with customers, potentially interacting with C-level personnel, and coordinating resources to craft tailored scientific solutions.
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The Regulatory Analyst 1 conducts on-site audits, reviews consolidated records, and designs/tests treatment matrices to identify potential cancers from claims data. Responsibilities also include overseeing the accurate and timely processing, tracking, and filing of federally mandated submissions.
The specialist will be responsible for identifying and engaging potential clients such as medical practices, hospitals, and research centers to expand the clinical trials network. This includes building strong relationships with decision-makers and developing strategic sales plans to drive growth.
The Site Management Associate I will assist in monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP guidelines. This role involves supporting site management activities such as documentation, data entry, tracking performance metrics, and collaborating with teams to resolve site-related issues.
The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will assess site performance, manage site-level activities, and support patient recruitment and retention strategies.
Lead technical pre-sales engagements with prospective customers and serve as the primary solution consultant. Collaborate with various teams to design tailored solutions and demonstrate Medable’s platform through live demos and technical deep dives.
Medical Director/Clinical Trial Physician(Rheumatology)
Thermo Fisher Scientific
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Full Time
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22 Weeks Ago
Thermo Fisher Scientific
Provide medical leadership to study teams and ensure the medical validity of clinical studies. Contribute to the creation and review of clinical trial protocols and ensure compliance with medical aspects.
Principal CRA – Lead Monitor (m/w/d)
Thermo Fisher Scientific
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Full Time
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22 Weeks Ago
Thermo Fisher Scientific
The Principal CRA will lead and coordinate all aspects of clinical monitoring and site management for complex trials, ensuring adherence to protocols, ICH-GCP, and regulatory requirements while acting as a subject-matter expert and escalation point. Key duties involve leading monitoring activities, performing site visits, overseeing data review, managing essential documents, and driving corrective actions.
Assistant CRA (m/f/d) (Open)
Thermo Fisher Scientific
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Full Time
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22 Weeks Ago
Thermo Fisher Scientific
The Assistant CRA will perform remote site management and monitoring activities, reviewing study data remotely and contacting sites to resolve issues and collect documentation. Responsibilities include maintaining communication with site staff regarding protocol conduction, enrollment, and performance indicators, and tracking study data in the EDC.
This role involves conducting day-to-day operations for clinical research recruitment and retention, supporting clinical studies from initiation through completion. The coordinator will collaborate closely with Principal Investigators, co-investigators, supervisors, other coordinators, clinic staff, and the HQ team.
Director, Medical Science Liaison, North Central
Celcuity Inc.
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Full Time
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22 Weeks Ago
Celcuity Inc.
The Director, MSL will be responsible for scientific exchange with healthcare providers and key decision-makers regarding Celcuity’s products and relevant disease states. They will also assist in identifying clinical trial sites and provide scientific training to internal colleagues.
The Director, MSL will be responsible for scientific exchange with healthcare providers and key decision-makers regarding Celcuity’s products and relevant disease states. They will also assist in identifying clinical trial sites and provide scientific training to internal colleagues.
Clinical Trial Manager (Associate Director) - London
Medpace, Inc.
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Full Time
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22 Weeks Ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain oversight of project team deliverables.
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The Flex Nurse Educator delivers essential remote educational support and medication training to patients with chronic diseases using various virtual platforms. This role also provides in-person education exclusively during territory vacancy coverage while maintaining high educational standards and compliance.
The Clinical Research Manager is accountable for end-to-end performance and project management for assigned protocols, ensuring compliance with regulations and quality standards. They serve as the main point of contact between country operations and the clinical trial team, leading local study teams and managing project deliverables.
Senior Clinical Research Associate
Translational Research in Oncology
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Full Time
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23 Weeks Ago
Translational Research in Oncology
Responsibilities include conducting various site visits such as pre-study, initiation, monitoring, and termination, while confirming adherence to all FDA, ICH-GCP, and local regulations. The role also involves ensuring the completion and collection of regulatory documents and performing data verification of source documents.
The Proposal Manager leads proposal teams in developing high-quality proposals for the U.S. government and other organizations. They manage the proposal process, ensuring compliance and timely submissions while collaborating with various stakeholders.
The Senior Clinical Informatics Sales Specialist will drive customer adoption and sales growth of Informatics products by providing technical guidance and expertise. They will consult with customers on informatics requirements and develop presentations to facilitate sales.
Account Manager, Language Services
Thermo Fisher Scientific
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Full Time
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23 Weeks Ago
Thermo Fisher Scientific
The Account Manager maintains relationships with key clients, serves as the initial communication point, and gathers complex client requirements. They also collaborate with production teams, advise clients on best practices, and troubleshoot issues during project processes.
The Flex Nurse Educator delivers remote patient education and medication training, primarily through virtual channels. They also provide in-person support during territory coverage, ensuring compliance and maintaining educational standards.
- Consulting Psychologist/Neurologist/Psychiatrist - General Interest
Cogstate
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Full Time
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23 Weeks Ago
Cogstate
Cogstate Clinicians are responsible for delivering remote clinical interviews and cognitive assessments to subjects with preclinical dementia. They also participate in regular clinical skill recalibration activities and review neuropsychological test batteries for data accuracy.
(Remote) Senior Research Scientist - Rockefeller Neuroscience Institute
West Virginia University
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Full Time
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23 Weeks Ago
West Virginia University
As a Senior Scientist, you will drive research projects and clinical trials focused on neurodegenerative diseases. You will design and oversee clinical studies, supervise researchers, and present findings at conferences.
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Clinical Research Associate (Home-based, Sydney)
Medpace, Inc.
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Full Time
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23 Weeks Ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols. Responsibilities also include communication with site staff, verifying investigator qualifications, and assessing patient recruitment success.
The Clinical Trial Manager will oversee the planning, execution, and successful completion of clinical trials while ensuring adherence to timelines, budgets, and regulatory guidelines. This role involves collaborating with cross-functional teams and managing site relationships to drive successful clinical trial outcomes.
The Senior Advisor guides regulatory and clinical strategies to ensure optimized, successful, timely commercialization of the product portfolio in the United States, involving various FDA submissions like 510(k)s, PMAs, and IDEs. This role also provides expert advice and support for necessary clinical research, contributing significantly to study design and acting as a subject matter expert for US regulatory and clinical questions across global product development centers.
Senior Patient Recruitment & Engagement Lead
Thermo Fisher Scientific
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Full Time
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23 Weeks Ago
Thermo Fisher Scientific
The Senior Patient Recruitment and Engagement Lead is responsible for leading multiple global studies and implementing strategies for recruitment and retention. This includes developing patient recruitment strategies, managing third-party vendors, and ensuring compliance with diversity requirements.
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