The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
Remote Clinical Research Jobs (607)
Tags = clinical-research
Act as a strategic liaison between ICON and investigator sites to strengthen relationships and support study performance. Responsibilities include managing site communication, monitoring performance metrics, and collaborating with project teams to align site capabilities with study opportunities.
The role involves authoring clinical pharmacology trial protocols and performing PK/PD analyses using non-compartmental methods. The scientist will also develop analysis plans and contribute to the drafting of Clinical Study Reports.
Associate Director, Business Development – Real World Evidence (RWE), LATAM
IQVIA
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Full Time
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4 Days Ago
IQVIA
Lead business development and growth strategies for Real World Evidence solutions across LATAM, with a primary focus on Brazil. Manage the full sales cycle and lead a team of business development resources to secure and retain pharmaceutical and healthcare clients.
Clinical Project Manager / Senior Clinical Project Manager
Precision for Medicine
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Full Time
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4 Days Ago
Precision for Medicine
Lead full-service clinical trials in Oncology, overseeing functional departments to ensure timelines, scope, cost, and quality are met. Act as the primary client liaison and manage the full study lifecycle from proposal and bid defense to completion.
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Clinical Project Manager / Senior Clinical Project Manager
Precision Medicine Group
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Full Time
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4 Days Ago
Precision Medicine Group
Lead and oversee full-service global clinical trials in Oncology, managing timelines, scope, cost, and quality. Act as the primary client liaison and coordinate cross-functional teams across data management, safety, and biostatistics.
Manage day-to-day clinical trial operations, ensuring adherence to timelines, budgets, and quality standards. Collaborate with cross-functional teams and investigators to implement protocols and ensure regulatory compliance.
Manage day-to-day clinical trial operations, ensuring adherence to timelines, budgets, and quality standards. Collaborate with cross-functional teams and investigators to implement protocols and maintain regulatory compliance.
Lead the initiation of clinical trials by preparing and submitting regulatory documents and coordinating with stakeholders for study approvals. Manage accurate records of submissions and provide guidance to study teams on regulatory best practices.
Lead end-to-end data management for complex global clinical trials from setup to database lock. Serve as the primary client contact while managing timelines, budgets, and mentoring junior staff.
Design, develop, and validate statistical, machine learning, and AI models to analyze complex clinical trial data. Collaborate with cross-functional teams to transform business challenges into production-ready analytical solutions and communicate findings to stakeholders.
Lead study-level vendor set-up and readiness activities to ensure the quality and integrity of data generated by external clinical research vendors. Translate protocol requirements into vendor specifications and manage the interface between the study team and vendors.
Lead the design and implementation of advanced data science methodologies and statistical models to optimize clinical research and trial outcomes. Coordinate delivery, guide a team of data scientists, and communicate complex insights to senior leadership and stakeholders.
The Project Management Analyst supports clinical trial delivery by managing project schedules, finances, and risk mitigation strategies. They are responsible for maintaining performance dashboards, ensuring eTMF compliance, and coordinating communication between project leaders and customers.
CRA Level II 17 APPLICANTS
Thermo Fisher Scientific
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Full Time
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21 Weeks Ago
Thermo Fisher Scientific
The Clinical Research Associate (Level II) will conduct remote or on-site monitoring visits to assess protocol and regulatory compliance, manage required documentation, and ensure trials adhere to approved guidelines. Key duties include applying risk-based monitoring approaches, performing root cause analysis for site failures, and maintaining communication with investigative sites, clients, and the project team.
The Flex Nurse Educator delivers essential remote educational support and medication training to patients with chronic diseases via various virtual channels, providing in-person education only when covering territory vacancies. Key duties include facilitating connections to approved resources, encouraging dialogue between patients and healthcare providers, and maintaining accurate documentation while upholding compliance standards.
Project Leadership – Biotech (Clinical Trials) - GLP-1 / Obesity - Home Based
Parexel
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Full Time
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21 Weeks Ago
Parexel
Individuals selected for these roles will provide leadership to project teams and manage the day-to-day operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality.
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Clinical Research Manager (Neurology)
Johns Hopkins University
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Full Time
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21 Weeks Ago
Johns Hopkins University
The Clinical Research Manager will manage the administrative and scientific implementation of complex clinical protocols or multiple studies, collaborating with faculty to develop protocols and SOPs while supervising study-related activities. Key duties include accountability for grant submission, administration, and ensuring regulatory compliance across single or multi-center sites.
Senior Director, Clinical Development
Definium Therapeutics
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Full Time
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21 Weeks Ago
Definium Therapeutics
The Senior Director will provide clinical science leadership, managing the design, planning, and execution of clinical trial programs with minimal guidance, and leading study design, implementation, and execution for assigned programs. This role involves serving as a major contributor to protocols, data interpretation, final reports, and overseeing medical monitoring activities for all human clinical trials.
VP, Clinical Science
Telix Pharmaceuticals (AMER)
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Full Time
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21 Weeks Ago
Telix Pharmaceuticals (AMER)
This senior leadership role supports the design, strategy, and operationalization of clinical trials from Phase 0 to Phase 4 by leading a team of subject matter experts in physics, pharmacology, imaging, and biostatistics. The VP will also function as an expert facilitator to asset matrix teams and advise other parts of the organization through formal consultation.
Clinical Research Associate / Senior Clinical Research Associate
PSI CRO
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Full Time
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21 Weeks Ago
PSI CRO
The Clinical Research Associate will conduct and report all types of onsite and remote monitoring visits, perform CRF review, source document verification, and manage site communication. Responsibilities also include involvement in site identification and potentially assisting in training less experienced CRAs.
The manager will lead and coordinate program planning and development activities, providing technical guidance, identifying program needs, and recommending new research initiatives based on expertise in informatics, data science, and clinical research. Responsibilities also include conducting scientific reviews of proposals, managing grants/contracts, and disseminating information through organizing workshops and serving as a scientific liaison.
Clinical Research Specialist II
University of Rochester
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Full Time
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21 Weeks Ago
University of Rochester
The interventionist will conduct Cognitive Behavioral Therapy for Treatment-Seeking with Deaf Individuals (Deaf CBT-TS) intervention sessions remotely via Zoom with Deaf participants, ensuring participant well-being and adherence to ethical principles. Responsibilities also include coordinating scheduling, managing participant inquiries, recording session notes, and following up with written action plans and resources.
Clinical Research Specialist II
University of Rochester
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Full Time
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21 Weeks Ago
University of Rochester
The interventionist will conduct Cognitive Behavioral Therapy for Treatment-Seeking with Deaf Individuals (Deaf CBT-TS) intervention sessions remotely via Zoom with Deaf participants, ensuring participant well-being and adherence to protocol. This includes coordinating scheduling, maintaining rapport, recording sessions, and following up with resources and action plans.
The manager will lead regulatory activities and submissions independently, providing regulatory guidance and operational support across various stages of drug development, including agency interactions and clinical trial applications. They will also contribute to developing best practices within ICON Regulatory Affairs based on regulatory process insights.
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.
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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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