Virtual Family Nurse Practitioner - CO Licensed
Provide virtual clinical care through telephonic triage, video visits, and email follow-ups. Collaborate with in-office and virtual teammates to deliver evidence-based primary care.
Remote Clinical Research Jobs (2,591)
Virtual Nurse Practitioner - WA Licensed
Provide virtual clinical care through tele-health visits, including telephonic triage, video appointments, and email follow-ups. Collaborate with virtual and in-office teammates while participating in weekly clinical rounds to ensure high-quality patient outcomes.
Virtual Family Nurse Practitioner - MA Licensed
Treat patients through tele-health visits, including telephonic triage, video appointments, and email follow-ups. Collaborate with virtual and in-office teammates while participating in continuous clinical learning.
Virtual Family Nurse Practitioner - IL Licensed
Provide virtual clinical care through telephonic triage, video visits, and email follow-ups to patients. Collaborate with virtual and in-office teams while participating in continuous learning through clinical rounds.
Virtual Physician Assistant - GA Licensed
The physician assistant will provide virtual clinical care through tele-health visits, including triage calls, video appointments, and email follow-ups. They will collaborate with a multidisciplinary team to deliver evidence-based primary care to patients.
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Virtual Family Nurse Practitioner - GA Licensed
Treat patients through tele-health visits, including video appointments, telephonic triage, and email follow-ups. Collaborate with virtual and in-office team members to provide evidence-based primary care.
Coder Inpatient
The Coder Inpatient is responsible for abstracting, coding, and sequencing clinical information from medical records to ensure accurate reimbursement and compliance. They must maintain high quality standards while utilizing coding software to process inpatient, outpatient, and emergency department records.
Clinical Data Risk Analyst
You will conduct risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies. Additionally, you will monitor data quality throughout the trial process and collaborate with cross-functional teams to implement risk management plans.
Imaging Research Associate I
The Imaging Research Associate coordinates site and operational activities throughout the clinical study lifecycle to ensure high-quality data delivery. They are responsible for managing site communications, processing study data, resolving discrepancies, and supporting project managers with administrative tasks.
Vice President, Medical Affairs
The Vice President of Medical Affairs will provide unified leadership for Medical Monitoring and Pharmacovigilance functions, overseeing strategy, P&L, and regulatory compliance. The role involves driving business development, managing client relationships, and advising the Chief Medical & Scientific Officer on medical and safety risks.
Associate Director, MedTech Delivery & Customer Success
The Associate Director oversees end-to-end delivery, governance, and optimization of IQVIA information assets for key MedTech accounts. They serve as the primary point of accountability for client satisfaction, issue resolution, and driving incremental growth through expanded solution utilization.
Senior Clinical Project Manager
The Senior Clinical Project Manager drives clinical ophthalmic projects by managing cross-functional teams, budgets, and timelines to ensure compliance with regulations. They also provide operational oversight, mentor junior staff, and coordinate with various internal and external stakeholders to deliver high-quality clinical trials.
Senior Clinical Research Associate
The Senior Clinical Research Associate manages clinical site relationships and ensures protocol compliance through monitoring activities and site oversight. They are responsible for site readiness, data accuracy, and maintaining regulatory documentation throughout the clinical trial lifecycle.
Clinical Research Associate II or Senior Clinical Research Associate
The Clinical Research Associate is responsible for managing clinical site relationships, ensuring protocol compliance, and maintaining data integrity throughout the trial lifecycle. They will conduct site visits, oversee patient safety, and drive recruitment strategies to meet project timelines.
Senior Clinical Research Associate - Spain - Remote
The Senior Clinical Research Associate is responsible for site qualification, initiation, monitoring, and study close-out visits to ensure clinical programs are executed with quality. They also provide mentoring to less experienced staff and ensure site compliance with protocols and data integrity.
Director Project Management - Rare Disease & Pediatrics - Europe
Acts as the primary client lead for complex clinical studies, driving operational delivery and managing risk across multiple vendors. Oversees project teams, ensures adherence to regulatory standards, and provides mentorship and talent development for project management staff.
Senior Clinical Trial Specialist (Contract)
The Senior Clinical Trial Specialist supports the planning and execution of clinical studies by managing site start-up, tracking study metrics, and coordinating team meetings. They also assist in the oversight of study vendors, maintenance of the Trial Master File (TMF), and data cleaning processes.
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CRA II
Manage site qualification, initiation, monitoring, and close-out activities for early-phase clinical studies. Build strong partnerships with investigators to ensure patient safety, protocol compliance, and data integrity.
Pharmacovigilance Regulatory Reporting Specialist
The specialist will process, assess, and submit safety reports to regulatory authorities in compliance with SOPs and project requirements. They will also liaise with functional team members and healthcare professionals to address project-related issues and report quality findings to senior staff.
Senior CRA level II
You will perform and coordinate clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory standards. Additionally, you will manage site relationships, conduct risk-based monitoring, and mentor junior team members to ensure data reliability and audit readiness.
Clinical Research Associate II
The Clinical Research Associate acts as the primary liaison between the project team and clinical sites to ensure study conduct meets quality and regulatory standards. Responsibilities include performing site monitoring visits, managing data integrity, and overseeing the accountability of investigational products.
Site Start-up Specialist - FSP
The Site Start-up Specialist coordinates site start-up activities, manages essential regulatory documents, and ensures compliance with ICH/GCP guidelines. They serve as the primary contact for investigative sites and assist in the negotiation of site contracts and budgets.
Clinical Research Associate - FSP - Sweden
The Clinical Research Associate monitors investigator sites using a risk-based approach to ensure data accuracy, protocol compliance, and regulatory adherence. They are responsible for site initiation, ongoing monitoring, issue resolution, and trial close-out activities while maintaining effective communication with investigative sites.
Regulatory and Start Up Specialist 1 (m/w/d) Home Based Germany
The Regulatory and Start-Up Specialist manages site identification, regulatory documentation, and contract negotiations to ensure clinical trial start-up activities are completed on time. They serve as the primary point of contact for investigative sites and ensure all activities adhere to SOPs and project requirements.
Clinical Data Coordinator - Senior
You will lead clinical research tasks by creating data management plans and ensuring compliance with regulatory standards. Additionally, you will collaborate with cross-functional teams to resolve data discrepancies and mentor junior staff on data cleaning procedures.
Clinical Research Billing Analyst
The Clinical Research Billing Analyst oversees the financial aspects of clinical trials, including Medicare Coverage Analysis and budget alignment. They manage research funds, conduct financial data analysis, and provide education to staff regarding billing processes and regulatory compliance.
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Senior Clinical Research Associate (CRA) - Remote in Sao Paulo
The Clinical Research Associate conducts qualification, initiation, monitoring, and closeout visits for research sites to ensure protocol compliance. They also manage communication with site staff, verify investigator qualifications, and ensure accurate data reporting in accordance with regulatory requirements.
CTC-L II
Provides administrative and technical support to the project team, including site activation activities and audit readiness. Manages clinical trial documentation, ensures system databases are current, and coordinates with internal departments to meet project deadlines.
CRA II
Performs and coordinates all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance. Conducts remote or on-site visits to assess data accuracy, manage documentation, and maintain collaborative relationships with investigational sites.
ACRA
The Assistant Clinical Research Associate provides logistical and administrative support for clinical trial site management and remote monitoring activities. Responsibilities include verifying document collection, managing site supplies, and assisting with study-specific systems and vendor coordination.
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