Remote Clinical Research Jobs

606 Clinical Research jobs available for remote work from home. Apply for positions such as Community IBC Member (Augusta), Informed Consent Writer, CRA II and SR CRA, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.

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Remote Clinical Research Jobs (606)

Tags = clinical-research
Sitero LLC is hiring for remote Community IBC Member (Augusta)

Community IBC Member (Augusta)

Sitero LLC · Full Time · 3 Days Ago
Sitero LLC
🌎 United States πŸ’΅ $110 - $125 per day ⭐ 5-10 yrs exp πŸ’Ό Others
The member reviews research protocols and monitors regulatory compliance to ensure the protection of participants, animals, and biosafety standards. They provide recommendations for the approval or termination of studies and assess risks associated with hazardous biological work.

Vice President, Imaging

ICON plc · Full Time · 3 Days Ago
ICON plc
🌎 Ireland, United States ⭐ 10+ yrs exp πŸ’Ό Others
Serve as a senior strategic leader driving business growth and strengthening sponsor relationships within medical imaging and cardiac safety services. Provide expert guidance on study strategy, operational delivery, and scientific innovation for global clinical development programs.

FSP Principal Biostatistician, Safety Analytics

IQVIA · Full Time · 3 Days Ago
IQVIA
🌎 United States πŸ’΅ $111K - $309K per year ⭐ 5-10 yrs exp πŸ’Ό Software Development
Provide statistical leadership and support for safety endpoints and outcomes in Phase 1, 2, and 3 pharmaceutical clinical trials. Develop ADaM/TFL standards, write statistical sections of protocols, and contribute to regulatory documents such as NDAs and DSURs.

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Thermo Fisher Scientific is hiring for remote Partnership Solutions Lead, Director -US Remote

Partnership Solutions Lead, Director -US Remote

Thermo Fisher Scientific · Full Time · 3 Days Ago
Thermo Fisher Scientific
🌎 United States ⭐ 10+ yrs exp πŸ’Ό Others
The Strategic Partnership Director is responsible for architecting and leading strategic partnership pursuits across Biopharma and Biotech. This includes developing governance frameworks, operating models, and executive-level narratives to differentiate the company in competitive environments.

Sr Clinical Research Associate

Veranex, Inc. · Full Time · 3 Days Ago
Veranex, Inc.
🌎 United States πŸ’΅ $98400 - $140K per year ⭐ 5-10 yrs exp πŸ’Ό Healthcare
The Sr. CRA is responsible for monitoring clinical trials to ensure adherence to protocols, regulations, and SOPs while acting as the primary liaison to clinical sites. Key duties include conducting site visits, verifying source data, and contributing to the development of study plans and regulatory reports.

Senior Statistical Programmer

Everest Clinical Research · Full Time · 3 Days Ago
Everest Clinical Research
🌎 United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Software Development
Design and specify study data tabulation and analysis models for clinical trials in accordance with industry standards. Develop SAS programming codes to generate accurate statistical output reports and provide technical guidance to junior programmers.

Project Manager, Contracts & Operations

Lupus Research Alliance Inc. · Full Time · 3 Days Ago
Lupus Research Alliance Inc.
🌎 United States πŸ’΅ $75000 - $85000 per year ⭐ 2-5 yrs exp πŸ’Ό Product Project Manager
The role involves managing cross-functional projects and administering the contracting process for Lupus Therapeutics. Key duties include preparing agreements, tracking budgets, and coordinating with biopharmaceutical partners and outside counsel.
UOMUOMUS is hiring for remote Regulatory Analyst 1

Regulatory Analyst 1

UOMUOMUS · Full Time · 3 Days Ago
UOMUOMUS
🌎 United States ⭐ 0-2 yrs exp πŸ’Ό Legal
The Regulatory Analyst conducts on-site audits and manages the submission of regulatory documents to the Institutional Review Board (IRB) for various clinical trials. They are responsible for maintaining regulatory binders, ensuring protocol compliance with federal regulations, and supporting investigators with research compliance.

Senior Proposals Development Associate

ICON plc · Full Time · 3 Days Ago
ICON plc
🌎 United States ⭐ 5-10 yrs exp πŸ’Ό Others
Facilitate the development and preparation of high-quality proposals for clinical trials by collaborating with cross-functional teams and subject matter experts. Manage timelines, ensure compliance with client requirements, and mentor colleagues in the proposal process.

Senior Site Contract Associate - IQVIA Biotech

IQVIA · Full Time · 3 Days Ago
IQVIA
🌎 Bulgaria, Hungary, Oman, Romania ⭐ 5-10 yrs exp πŸ’Ό Others
Manage start-up contracting activities, including the development of investigator grant estimates and proposal text for biotech sponsors. Ensure overall contracting efficiency and adherence to project timelines while maintaining internal systems like CTMS.
Thermo Fisher Scientific is hiring for remote Site Recruiter - CorEvitas

Site Recruiter - CorEvitas

Thermo Fisher Scientific · Full Time · 3 Days Ago
Thermo Fisher Scientific
🌎 United States πŸ’΅ $83300 - $125K per year ⭐ 5-10 yrs exp πŸ’Ό Recruitment Recruiter
Support the identification, recruitment, and activation of investigator sites across multiple clinical registries to meet study timelines. Manage site feasibility assessments, onboarding documentation, and maintain recruitment metrics using Salesforce and other BI tools.

Auditor/Educator Physician

Omega Healthcare Solutions · Full Time · 3 Days Ago
Omega Healthcare Solutions
🌎 United States πŸ’΅ $35.5 - $51.5 per hour ⭐ 5-10 yrs exp πŸ’Ό Finance Auditor
The Auditor/Educator Physician reviews medical records for coding accuracy and provides feedback and education to improve documentation. They also create action plans and training materials to address coding problems and documentation gaps.

Auditor/Educator In/Outpatient

Omega Healthcare Solutions · Full Time · 3 Days Ago
Omega Healthcare Solutions
🌎 United States πŸ’΅ $38.5 - $58 per hour ⭐ 5-10 yrs exp πŸ’Ό Finance Auditor
Review medical records for coding accuracy and provide feedback to coders and providers. Deliver education to improve documentation and coding practices.

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Akero Therapeutics is hiring for remote Clinical TMF Operations Administrator

Clinical TMF Operations Administrator

Akero Therapeutics · Full Time · 3 Days Ago
Akero Therapeutics
🌎 Worldwide πŸ’΅ $99600 - $155K per year ⭐ 2-5 yrs exp πŸ’Ό Software Development
Lead TMF activities across all trial phases, ensuring inspection readiness and compliance with the TMF Reference Model. Oversee eTMF health, manage quality issue workflows, and collaborate with CROs and clinical trial teams to maintain accurate records.

Medical Science Liaison, Global Rare Diseases - Midwest

Chiesi Group · Full Time · 3 Days Ago
Chiesi Group
🌎 United States πŸ’΅ $142K - $173K per year ⭐ 2-5 yrs exp πŸ’Ό Healthcare
The Medical Science Liaison (MSL) is responsible for building partnerships with key opinion leaders and engaging in scientific exchanges with external stakeholders. This includes providing medical support, delivering education, and fostering collaborations in the assigned therapeutic areas.

Senior CRA

ICON plc · Full Time · 3 Days Ago
ICON plc
🌎 Poland ⭐ 5-10 yrs exp πŸ’Ό Others
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.
🌎 Italy πŸ’΅ €33000 - €61400 per year ⭐ 2-5 yrs exp πŸ’Ό Others
As a Regulatory & Start-Up Specialist, you will lead complex projects and serve as the Single Point of Contact for investigative sites and project teams. You will prepare submission documents, perform site activation activities, and ensure adherence to regulations and project timelines.

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🌎 Poland πŸ’΅ 171K - 404K per year ⭐ 2-5 yrs exp πŸ’Ό Others
The Global Trial Manager will oversee critical aspects of late-phase clinical trials, ensuring they meet timelines, budgets, and quality standards. Responsibilities include drafting clinical documentation, managing project leadership tasks, and coordinating vendor and stakeholder management.
🌎 Canada πŸ’΅ 99500 - 132K per year ⭐ 5-10 yrs exp πŸ’Ό Writing Medical Writer
Acts as Lead Medical Writer on various writing projects, preparing documents according to SOPs and customer requirements. Provides feedback to junior staff and manages timelines and client communications.
🌎 France, Netherlands, Spain, Ukraine, United Kingdom ⭐ 5-10 yrs exp πŸ’Ό Software Development
The Senior Statistical Programmer is responsible for reviewing datasets and ensuring submission readiness of clinical data. They will collaborate with study teams to design data structures and oversee the development of SAS programs for clinical data analysis.

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