Conduct standardized remote clinical interviews and psychiatric assessments for participants in a PTSD clinical research study. Ensure protocol compliance, data quality, and the accurate scoring of study-specific rating scales.
Remote Clinical Research Jobs (1,576)
Tags = clinical-research
The specialist is responsible for the definition, set-up, and ingestion of external data streams in alignment with clinical trial protocols. This includes developing Data Transfer Agreements and performing UAT to ensure data accuracy and consistency.
Site Contracts Lead - Europe - Remote
Worldwide Clinical Trials
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Full Time
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1 Week Ago
Worldwide Clinical Trials
Serve as the primary point of contact for project teams and sponsors regarding study site contracting activities. Lead and mentor site contracts specialists while negotiating and finalizing clinical trial agreements and budgets.
Lead performance and compliance for assigned clinical trial sites, ensuring rigorous adherence to ICH/GCP and local regulatory requirements. Perform site management, monitoring activities, and maintain strong relationships with investigators throughout all study phases.
The role involves negotiating clinical trial agreements, budgets, and payment terms directly with assigned sites. It also requires collaborating with internal teams to improve SB&C metrics and ensuring standards are applied across projects.
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Acts as the primary point of contact for clients regarding live eCOA studies and manages project scope, plans, and schedules. Leads client update meetings, manages system change efforts, and handles project documentation and budgeting.
Territory Manager, Structural Heart – Structural Interventions (New York City)
Abbott
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Full Time
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1 Week Ago
Abbott
The Territory Manager is responsible for meeting sales objectives for Structural Heart products by identifying market opportunities and developing sales strategies. This includes conducting sales calls, observing clinical procedures in labs, and educating healthcare professionals on product usage.
Director, Medical Science Liaison, GI (IL, IN)
Revolution Medicines
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Full Time
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1 Week Ago
Revolution Medicines
The Medical Science Liaison will cultivate professional relationships with key opinion leaders and healthcare providers to advance scientific knowledge in GI oncology. They will also serve as a therapeutic expert, providing scientific support for clinical development, medical congresses, and internal cross-functional teams.
The MSL serves as the external scientific face of the company, developing relationships with Thought Leaders to facilitate information exchange and education on therapies. They are responsible for gathering field insights to refine company strategies and supporting clinical research activities.
The specialist serves as the single point of contact for site activation activities, ensuring adherence to regulations and project timelines. Responsibilities include preparing regulatory documents, tracking approvals, and performing quality control on site deliverables.
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.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and collaborate with cross-functional teams for accurate data collection.
The role involves managing invoicing, account reconciliation, and contract progression for a portfolio of accounts. It also requires negotiating clinical trial agreements and budgets with sites while collaborating with internal study startup and revenue teams.
Senior Clinical Research Associate - Oncology - Northeast/Midwest (Remote)
Worldwide Clinical Trials
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Full Time
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1 Week Ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with informed consent and regulatory requirements.
Senior Clinical Research Associate - CNS - Midwest (Remote)
Worldwide Clinical Trials
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Full Time
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1 Week Ago
Worldwide Clinical Trials
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Provide logistical and administrative support for site preparedness and remote monitoring in accordance with SOPs and regulatory guidelines. Assist CRAs with site management tasks, document collection, and the reconciliation of study data.
Clinical Safety Data Associate
Everest Clinical Research
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Full Time
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1 Week Ago
Everest Clinical Research
Develop and execute safety data review plans for clinical trials, focusing on AEs, SAEs, and laboratory data. Perform medical coding using MedDRA and WHODrug dictionaries while coordinating with data managers to ensure high-quality data collection.
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Lead the growth and success of commercial eClinical and Clinical services by generating new leads and nurturing long-term client relationships. Manage the full customer lifecycle from onboarding and procurement to financial management and issue escalation.
Lead and oversee end-to-end study start-up activities, including site identification, regulatory submissions, and site activation. Manage a team of professionals while collaborating with sponsors and regulatory teams to ensure compliance and timely trial initiation.
Oversees domestic and global Phase I clinical projects, managing scope, schedule, cost, and quality to meet client expectations. Leads cross-functional teams and handles risk assurance, regulatory documentation, and potential line management duties.
Clinical Team Manager/Sr. (CTM) - FSP
Thermo Fisher Scientific
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Full Time
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1 Week Ago
Thermo Fisher Scientific
Accountable for achieving final clinical deliverables and clean data within contract timelines and budgets. Manages monitoring operations, quality compliance, and coordinates with study sites and sponsors.
Responsible for the design, execution, and scientific oversight of clinical research studies for new or marketed drugs. This includes developing clinical development plans, authoring regulatory documents, and managing medical monitoring to ensure patient safety.
Provide logistical and administrative support for clinical trial site preparedness and remote monitoring activities. Assist CRAs with site management, document verification, and the coordination of study supplies and payments.
Provide logistical and administrative support for clinical trial site management and remote monitoring activities. Assist CRAs with site preparedness, document collection, and the reconciliation of study data in accordance with SOPs.
Provide logistical and administrative support for clinical trial site preparedness and remote monitoring in accordance with SOPs. Assist CRAs with site management tasks, document collection, and the reconciliation of study data.
Provide logistical and administrative support for site preparedness and remote monitoring in accordance with SOPs and regulatory guidelines. Assist CRAs with site management tasks, document collection, and the reconciliation of study data.
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Coordinate site-level document collection and maintenance to ensure compliance and efficiency during clinical study start-up. Act as an operational liaison for site staff and provide guidance to junior Site Specialists.
Independently manage the negotiation and execution of clinical trial agreements and budgets for various studies. Collaborate with internal stakeholders and investigator sites to ensure compliant and efficient study start-up.
Manage Site Enrollment and Engagement Lead (SEEL) teams to optimize clinical trial enrollment and ensure compliance with regulations. Provide operational delivery of team strategies, conduct performance reviews, and deliver regular project updates to stakeholders.
Serve as a scientific liaison to the medical community by building relationships with thought leaders and clinicians. Communicate scientific information and manage external clinical research collaborations and investigator-initiated trials.
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