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 and payments.
Remote Clinical Research Jobs (1,576)
Tags = clinical-research
The CRA II acts as the primary liaison between the project team, sponsor, and clinical sites to ensure high-quality study conduct. Responsibilities include performing site selection, initiation, routine monitoring, and close-out visits while ensuring data integrity and compliance.
Provide strategic leadership in the design and implementation of eCOA clinical systems and technologies for a pharmaceutical sponsor. Manage eCOA vendor relationships, lead study-specific technology deployment, and ensure deliverables meet quality and timeline expectations.
The Clinical Development Trial Lead manages cross-functional teams to execute clinical trials on time, within scope, and within budget. They are responsible for trial enrollment strategies, risk mitigation, and maintaining the Trial Master File for inspection readiness.
The Senior CRA is responsible for investigative site management and monitoring activities throughout the clinical trial lifecycle for Oncology trials. Key duties include ensuring data integrity, subject safety, and maintaining a continuous state of inspection readiness.
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Oversee the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies. Coordinate contract management workstreams and serve as the primary escalation point for contract issues.
Provides scientific and medical guidance to operational teams and contributes expert input on RFPs, RFIs, and study execution strategies. Responsible for reviewing medical data and delivering therapeutic training materials.
Clinical Research Specialist Operations Manager
N-Power Medicine
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Full Time
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1 Week Ago
N-Power Medicine
Lead the daily operations, performance, and compliance of Clinical Research Specialist staff across designated health system accounts. Serve as the primary operational liaison to ensure high-quality service delivery and maintain strong customer relationships with health system partners.
The Clinical Project Manager II is responsible for the operational strategy, budget, and timeline of Phase I clinical trials. They lead high-performing matrixed teams to ensure project delivery meets quality standards and customer needs.
Senior Pharmacovigilance System Architect (Argus Administrator) India, Remote (5pm to 2am IST)
MMS
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Full Time
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1 Week Ago
MMS
Serves as the Database Administrator for Argus Safety, managing configuration, maintenance, and E2B reporting via gateway technologies. Provides technical leadership for system upgrades, case migrations, and ensures alignment with global regulatory requirements.
Responsible for overseeing site management, clinical monitoring, and data integrity to ensure patient safety and regulatory compliance. Collaborates with functional leaders to manage study milestones, risk mitigations, and the development of clinical study tools.
Manage and grow client relationships to drive revenue growth and ensure client satisfaction within the eClinical industry. Develop annual business plans and execute strategies to penetrate pharmaceutical, biotechnology, and medical device companies.
Leads data management operations across a multi-site research network to ensure data quality, integrity, and operational visibility. Supervises a remote team of Data Entry Specialists and collaborates with clinical operations to optimize source documentation and data capture workflows.
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.
Country Activation and Submission Representative (Home-Based, Poland) - IQVIA Biotech
IQVIA
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Full Time
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1 Week Ago
IQVIA
Manage country-level regulatory and site activation activities for clinical studies in Poland, including EU CTR submissions and amendments. Coordinate with investigative sites and regulatory authorities to ensure compliance and timely study start-up and maintenance.
Senior Clinical Research Associate - Oncology - Florida (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.
Clinical Team Manager, Respiratory
Thermo Fisher Scientific
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Full Time
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1 Week Ago
Thermo Fisher Scientific
The Clinical Team Manager oversees all clinical operational and quality aspects of respiratory studies in compliance with ICH-GCP. This includes developing monitoring strategies, managing project financials, and leading clinical teams to ensure deliverables are met within contractual timelines.
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The Project Support Specialist provides cross-functional support to ensure efficient management of clinical studies, including maintaining timelines and managing study documentation. Key tasks include coordinating meetings, managing CTMS data, and overseeing study-specific training and supplies.
Project Support Specialist
Precision Medicine Group
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Full Time
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1 Week Ago
Precision Medicine Group
The Project Support Specialist provides cross-functional support for clinical studies, including managing project timelines, scheduling meetings, and maintaining the Trial Master File. They are also responsible for CTMS updates, training record management, and coordinating study supplies and communications.
Lead the initiation and activation of clinical trials by managing site-related essential document collection and review. Collaborate with internal teams and CROs to improve start-up metrics and ensure eTMF accuracy.
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.
Facilitate site start-up and activation by managing essential document collection and reviewing site-level Informed Consent Forms. Collaborate with internal teams and CROs to improve SSU metrics and ensure study timelines are achieved.
The role involves coordinating the setup and monitoring of clinical trials, ensuring accurate study status reports and documentation. It also requires maintaining strong relationships with stakeholders and ensuring compliance with regulatory requirements and patient safety.
The Clinical Risk Manager I will lead risk-based monitoring strategies, including the development of Integrated Quality Risk Management Plans and the identification of critical data and processes. They will serve as a subject matter expert to support cross-functional teams in mitigating protocol execution risks throughout the project life cycle.
Country Operations Lead - FSP, Germany (m/w/d)
Thermo Fisher Scientific
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Full Time
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1 Week Ago
Thermo Fisher Scientific
The role involves managing and mentoring Clinical Team Managers to ensure the successful execution of clinical deliverables within assigned projects. It also requires overseeing budgeting, resource allocation, and the implementation of performance metrics for the clinical management group.
Clinical Research Patient Phone Recruiter
Thermo Fisher Scientific
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Full Time
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1 Week Ago
Thermo Fisher Scientific
Conduct phone-based pre-screening interviews with prospective clinical trial participants to assess eligibility based on study protocols. Coordinate scheduling for qualified patients and maintain accurate medical records within clinical databases.
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Responsible for the design, scientific oversight, and execution of clinical research studies for new and marketed drugs. The role involves developing clinical development plans, managing medical monitoring, and collaborating on regulatory strategies for global submissions.
The Senior CRA manages communication with project stakeholders and maintains relationships with clinical sites to ensure research standards and timelines are met. Key duties include conducting onsite monitoring visits, performing data verification, and supervising study activities at the country level.
Lead the initiation and activation of clinical trials by managing essential document collection and review. Collaborate with internal teams and CROs to improve start-up metrics and ensure eTMF accuracy.
Spécialiste, rédaction de propositions/Proposal Writer Specialist
Indero
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Full Time
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1 Week Ago
Indero
Responsible for developing and writing scientific and technical content for study proposals and responding to RFIs. Coordinates with internal subject matter experts and external KOLs to ensure accurate, compelling, and compliant proposal delivery.
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