2,265 Clinical Research jobs available for remote work from home. Apply for positions such as Site Contracts Negotiator II, Senior Associate I, TMF Operations Fix term, Associate I, TMF Operations, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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You will independently manage the negotiation and execution of clinical trial agreements and budgets with UK investigator sites. This involves collaborating with cross-functional teams to ensure study start-up is efficient, compliant, and timely.
The Senior Associate will manage complex TMF studies, provide subject matter expertise, and oversee quality control processes to ensure regulatory compliance. They will also prepare TMF performance metrics and support project teams during audits and sponsor interactions.
The Associate will process, review, and resolve Trial Master File (TMF) documents while ensuring compliance with SOPs and industry regulations. They will also provide administrative support to the RMC Lead, including maintaining quality control checklists and tracking study documentation.
The Medical Writer will author, edit, and finalize high-quality expert reports and statistical analysis plans for cardiac safety studies. They will collaborate with cross-functional teams to interpret clinical data and ensure all documentation aligns with regulatory expectations.
The Coder Physician is responsible for abstracting, coding, and sequencing clinical information from various medical records to ensure accurate billing and reimbursement. They must maintain compliance with regulatory standards while meeting productivity and quality requirements.
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The Contract Analyst will negotiate site-related contracting items, including clinical trial agreements, budgets, and payment terms. They will also manage invoicing, reporting activities, and collaborate with internal teams to improve site budget and contract metrics.
You will lead clinical research tasks by creating data management plans, ensuring regulatory compliance, and resolving data discrepancies. Additionally, you will collaborate with cross-functional teams and mentor junior staff to maintain high data quality standards.
Perform site selection, initiation, monitoring, and close-out visits while ensuring compliance with regulatory requirements. Manage study progress by tracking regulatory submissions, recruitment, and data query resolutions.
The Clinical Project Manager is responsible for driving project performance, managing budgets, and ensuring adherence to timelines and quality standards throughout the clinical trial lifecycle. They will lead cross-functional teams, manage client relationships, and implement risk management strategies to ensure successful project delivery.
Lead and manage clinical project feasibility processes to support proposal teams and business development operations. Act as a technical expert for internal and external clients while ensuring adherence to regulatory standards and ICH-GCP principles.
The Contract Analyst will prepare and verify invoicing while managing a portfolio of clinical trial contracts and budgets. They will negotiate site-related agreements and collaborate with internal teams to ensure project timelines and metrics are met.
The SB&C Lead manages the development, negotiation, and execution of clinical trial agreements and site budgets to ensure timely study startup. They also act as an escalation point for budget issues and collaborate with internal teams to improve delivery metrics and processes.
The Clinical Research Associate coordinates clinical monitoring and site management processes to ensure trial compliance with protocols and regulatory standards. They perform risk-based monitoring, manage documentation, and facilitate communication between investigative sites and the project team.
The Senior Site Specialist serves as the primary operational contact for investigator sites, managing site start-up, maintenance, and close-out activities. They are responsible for ensuring accurate documentation, mentoring junior staff, and streamlining site workflows to improve clinical trial efficiency.
The Director, Safety Scientist leads the detection, evaluation, and management of safety signals for assigned compounds while ensuring compliance with global regulatory requirements. They provide clinical and scientific expertise to cross-functional teams and represent the safety department in regulatory interactions and governance meetings.
You will lead negotiations with investigative sites regarding clinical trial agreements, budgets, and payment schedules to ensure timely study activation. Additionally, you will collaborate with cross-functional teams to monitor progress, identify risks, and ensure all contracting activities align with regulatory standards and study timelines.
You will lead clinical trial initiation activities, including site essential document collection and review to ensure regulatory compliance. Additionally, you will collaborate with internal teams and CROs to track site activation timelines and resolve escalated issues.
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Develop and maintain C++ applications and database processes for payment and billing management in the healthcare sector. Implement legal requirements, automate testing, and refactor existing processes using modern technologies and agile methods.
The role involves monitoring investigator sites using a risk-based approach to ensure data accuracy and regulatory compliance. Responsibilities include conducting site initiations, close-outs, and mentoring new team members while maintaining communication between sites and clients.
The role involves managing contract activities, including negotiating clinical trial agreements and budgets with assigned sites. It also requires coordinating with internal teams to improve SB&C metrics and ensuring adherence to industry standards and fair market value guidance.
The Medical Director oversees the execution of clinical trials in Neuroimmunology, specifically focusing on Lupus SLE, for a top-5 pharma client. Responsibilities include developing clinical development plans, overseeing medical writing for protocols, and managing clinical teams and scientific risks.
Conduct study site monitoring visits to ensure compliance with protocols, GCP, and regulatory requirements. Manage the full site lifecycle from initiation to closeout while supporting patient safety and data integrity.
The CRA Level II is responsible for monitoring investigator sites to ensure protocol and regulatory compliance through on-site and remote visits. They manage site documentation, conduct data verification, and maintain collaborative relationships with investigative sites to guarantee subject safety and data reliability.
The CRA Level II is responsible for monitoring investigator sites to ensure protocol and regulatory compliance using a risk-based approach. They manage site documentation, conduct remote and on-site visits, and maintain collaborative relationships with investigative sites to guarantee data reliability.
Conduct remote and on-site monitoring visits to ensure clinical trials comply with protocols, ICH-GCP guidelines, and regulatory requirements. Manage site documentation, perform data verification, and maintain collaborative relationships with investigational sites.
The role involves negotiating clinical trial agreements, budgets, and payment terms directly with assigned sites. It also requires collaborating with internal teams to improve SB&C metrics and ensuring standards are applied across projects.
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Conduct standardized remote clinical interviews and psychiatric assessments for participants in a PTSD clinical research study. Ensure protocol compliance, data quality, and consistency while administering specific rating scales.
Conduct standardized remote clinical interviews and psychiatric assessments for participants in a PTSD clinical research study. Ensure protocol compliance, data quality, and the accurate scoring of study-specific rating scales.
Serve as the primary point of contact for project teams and sponsors regarding study site contracting activities. Lead and mentor site contracts specialists while negotiating and finalizing clinical trial agreements and budgets.
The Territory Manager is responsible for meeting sales objectives for Structural Heart products by identifying market opportunities and developing sales strategies. This includes conducting sales calls, observing clinical procedures in labs, and educating healthcare professionals on product usage.
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