The Clinical Trial Liaison supports clinical trials by providing scientific and clinical support to investigators and site staff. They also function as recruitment specialists to develop and optimize strategies for successful patient enrollment.
Remote Clinical Research Jobs (1,605)
Tags = clinical-research
Territory Manager, Structural Heart – Surgical Valves (St. Louis Missouri)
Abbott
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Full Time
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41 Weeks Ago
Abbott
Promote and support Abbott Structural Heart through business growth strategies and risk mitigation plans. Collaborate with healthcare providers to generate referrals and ensure good clinical outcomes for patients.
Agent de centre d'appels / Call Center Agent Bilingual French/English
IQVIA
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Full Time
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41 Weeks Ago
IQVIA
The Call Center Agent will conduct inbound and outbound calls to notify potentially affected facilities and maintain a high level of professionalism and confidentiality. They will also manage data entry and perform general clerical duties.
The Project Manager III will write requirements for assigned IRT studies and manage their implementation to ensure patients receive the correct study drug according to the Sponsor’s protocol. This role involves consulting with clients, managing timelines, and overseeing user acceptance testing.
The intern will assist in identifying, sourcing, and organizing public clinical datasets, as well as maintaining and updating internal dashboards. This role involves cataloging datasets and performing light preprocessing and data curation.
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The Site Payments Analyst ensures accurate and timely payments to clinical trial sites by monitoring payable items and validating invoices against completed services. They also participate in trial oversight meetings and coordinate with contract managers to maintain accurate payment terms.
Assist project managers in planning, execution, and monitoring of clinical trials. Coordinate study activities including site selection, patient recruitment, and data collection.
The Site Specialist II will work with Site Partners and internal stakeholders to optimize study performance and ensure successful site activation. They will support the collection and organization of start-up documentation and ensure compliance with applicable regulations and guidelines.
French speaking Medical information Specialist- graduate opportunity 11 APPLICANTS
ProPharma
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Full Time
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41 Weeks Ago
ProPharma
The role involves responding to medical and safety-related inquiries from healthcare professionals and patients, using approved product information to provide accurate responses. Additionally, the specialist will document adverse events and support service quality through checks and training of new team members.
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials while ensuring protocol compliance and patient safety. Collaborate with investigators and site staff to facilitate smooth study conduct and maintain high-quality clinical data.
Global Lead Credit Controller 11 APPLICANTS
Cerba Research
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Full Time
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42 Weeks Ago
Cerba Research
As the Global Credit Controller, you will own and optimize the global credit and collections process, ensuring timely cash collection and reduced DSO. You will develop and implement global credit control policies and procedures to minimize risk and strengthen financial discipline.
The Clinical Country Site Lead (CCSL) provides local operational and scientific expertise to support global clinical development strategy and ensures the delivery of local clinical trials. This role acts as a primary contact for CRO staff and global teams, focusing on quality, patient safety, and oversight of monitoring activities.
Lead and coordinate software delivery across IQVIA Connected Devices’ product teams, ensuring alignment of timelines, dependencies, risk management strategies, and release milestones. Act as a central point of contact for delivery status, blockers, and escalation across teams.
The Clinical Trial Liaison supports clinical trials by providing scientific and clinical support to investigators and site staff. They also function as recruitment specialists, developing strategies to drive successful patient enrollment.
Lead clinical trial start-up activities and oversee day-to-day delivery of site activation in assigned projects. Ensure adherence to sponsor timelines and compliance with regulatory standards.
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