2,591 Clinical Research jobs available for remote work from home. Apply for positions such as Site Budgeting and Contracting Specialist - FSP, Principal Biostatistician, Site Management Associate II, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The specialist is responsible for preparing country site budgets, managing clinical trial agreement negotiations, and ensuring all financial exhibits are executed in compliance with legal standards. They will also act as a primary liaison between clinical trial sites, legal departments, and internal clinical operations teams to facilitate study start-up and ongoing budget maintenance.
The Principal Biostatistician will lead statistical efforts for clinical trials and provide expert guidance for regulatory submissions and product development. They are responsible for interpreting complex clinical data, mentoring junior staff, and ensuring the standardization of biostatistical processes.
The Site Management Associate II is responsible for investigative site recruitment, feasibility assessments, and remote clinical monitoring to ensure compliance with study protocols and regulatory standards. They also manage essential document collection, maintain the Trial Master File, and provide mentorship to junior staff members.
The Oncology Data Specialist is responsible for abstracting cancer cases into the registry database and ensuring compliance with state and national reporting standards. They also manage follow-up information, resolve data errors, and maintain accurate records for cancer patients.
The Clinical Payments Specialist manages end-to-end investigator payments, including setup, deployment, and reconciliation for assigned clinical studies. They act as a liaison between investigative sites and internal teams while ensuring payments align with clinical trial agreements and budgetary forecasts.
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The Chief Pharmacy & Procurement Officer is responsible for the enterprise-wide strategy, performance, and advancement of pharmacy operations, procurement, and medically integrated dispensing. This executive leader collaborates with cross-functional teams to ensure regulatory integrity, financial growth, and high-quality clinical outcomes across the organization.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while performing data review to maintain high-quality clinical study documentation.
The Senior Data Scientist will develop and implement machine learning models and analytical tools to support business intelligence and clinical research strategies. They will collaborate with functional teams to interpret data, monitor model performance, and provide innovative solutions to meet complex data modeling requirements.
The In-house CRA manages and supports clinical sites from approval through close-out to ensure trial data integrity. They are responsible for maintaining regulatory documentation, reviewing eCRF data, and ensuring protocol compliance in collaboration with field CRAs.
The Key Account Manager will drive sales growth and product adoption for genomic testing assays within the Lombardia Ovest region by engaging with oncologists, surgeons, and pathologists. They are responsible for developing local account plans, managing stakeholder relationships, and differentiating the product in a competitive market.
The Recall Analyst manages and coordinates recall projects by handling inbound and outbound calls with healthcare professionals. They are also responsible for maintaining project documentation and ensuring compliance with industry standards and regulations.
The Recall Analyst manages and coordinates recall projects by handling inbound and outbound calls with healthcare professionals. They are also responsible for maintaining project documentation and ensuring compliance with industry standards and regulations.
The Senior Clinical Research Associate executes clinical monitoring activities at trial sites, ensuring compliance with ICH-GCP guidelines and study protocols. They are responsible for site management, data quality oversight, and collaborating with clinical study teams to meet project timelines.
The Regulatory and Start Up Specialist is responsible for managing site activation readiness, including regulatory submissions, contract negotiations, and budget management. They ensure compliance with international and local regulations while maintaining project trackers and facilitating communication across clinical teams.
The Regulatory and Start Up Specialist is responsible for managing site activation readiness, including regulatory submissions, contract negotiations, and budget management. They act as a subject matter expert to ensure clinical trials comply with international and local regulations while maintaining audit readiness.
The Senior Quality Manager provides functional and project-level quality oversight to ensure compliance with GCP and GxP regulations. They are responsible for managing vendor quality, overseeing CAPA processes, and conducting audits of systems and clinical trials.
The Project Administrative Assistant will manage the administrative and financial aspects of COA licensing projects, including budget tracking and invoice coordination. They will also maintain project data, generate status reports, and liaise with internal and external stakeholders to ensure timely project delivery.
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The specialist is responsible for the timely and high-quality delivery of site activation readiness, including the preparation of clinical trial applications and submission dossiers. They will also manage communication with competent authorities and ethics committees while maintaining project trackers and regulatory intelligence tools.
The Regulatory and Site Start Up Specialist is responsible for managing site activation readiness, including preparing clinical trial applications and submission dossiers for regulatory bodies. They also facilitate communication between clinical teams and site stakeholders to ensure compliance with international and local regulations.
The Senior Medical Writer will lead the development of complex clinical documents such as regulatory submissions, protocols, and clinical study reports. They will also act as a primary technical contact for clients and provide senior-level review and guidance to junior staff.
The Medical Science Liaison serves as a field-based scientific expert, engaging with healthcare providers to provide education on investigational products and supporting research collaborations. They are responsible for identifying clinical research opportunities, maintaining relationships with oncology leaders, and contributing to medical strategy and internal cross-functional projects.
The Clinical Sales Specialist provides clinical and sales support by educating customers on structural heart products and providing technical assistance during procedures. They collaborate with territory managers to ensure optimal patient outcomes and support the implementation of product marketing strategies.
The Coder Inpatient is responsible for reviewing medical records and assigning accurate diagnostic and procedural codes for reimbursement and statistical analysis. They must maintain compliance with regulatory standards while ensuring high-quality data abstraction and documentation within specified systems.
The Associate Director will engage in the exchange of scientific data with key opinion leaders and healthcare providers to support medical strategy. They are responsible for identifying research gaps, supporting evidence generation, and reporting medical insights to inform internal partners.
The Coder Physician is responsible for abstracting, coding, and interpreting clinical information from various medical records to ensure accurate reimbursement and compliance. They must maintain productivity levels and quality ratings while adhering to HIPAA and regulatory standards.
The SMAO Line Manager is responsible for leading a regional team of Study Management Associates to ensure best-in-class clinical study execution. They provide mentorship, performance management, and strategic resource planning to support the professional growth of their team and organizational deliverables.
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The Regulatory Project Assistant provides administrative support for regulatory and eTMF operations, including managing documentation in the CTIS portal. They are responsible for tracking project timelines, preparing regulatory submissions, and maintaining trackers for clinical studies.
The manager will develop professional relationships with Key Opinion Leaders and provide regional scientific support for Shockwave Medical products. They will also oversee investigator-initiated studies and collaborate with cross-functional teams to ensure scientific evidence is effectively communicated.
The Senior Trial Manager oversees the planning, execution, and completion of clinical trials while ensuring compliance with ICH/GCP regulations. They lead the clinical operations team, manage vendor relationships, and monitor project deliverables to ensure quality and timely completion.
The Field Clinical Specialist provides procedural case support to physicians and hospital staff for intravascular lithotripsy technology. They also manage clinical study investigators, conduct device training, and ensure accurate data collection for clinical programs.
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