2,268 Clinical Research jobs available for remote work from home. Apply for positions such as Senior Clinical Project Manager, Clinical Research Associate - Cross TA, Clinical Research Associate - Start up - Cross TA, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The Senior Clinical Project Manager will lead and manage clinical projects, ensuring successful execution and delivery of objectives, particularly for radiopharmaceutical and radioligand-based programs. Responsibilities include developing project plans, leading cross-functional teams, and mentoring staff to foster a culture of excellence.
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting monitoring visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for maintaining clinical documentation, monitoring patient safety, and overseeing site-level recruitment and data integrity.
The Clinical Research Associate will manage site selection, activation, and regulatory compliance for clinical trials across various therapeutic areas. They will act as the primary point of contact for sites and study teams to ensure project milestones are met while maintaining high-quality documentation.
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, conduct site visits, and manage essential documentation to guarantee data reliability and subject well-being.
The role involves building and executing real-world evidence analyses using large-scale healthcare data to answer complex biopharma questions. You will also collaborate with AI and product teams to improve clinical research agents while serving as an embedded data scientist for partner institutions.
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The Clinical Information Specialist will design and implement virtual training programs for clinical staff while managing database reporting and clinical research. They are responsible for maintaining medical records and ensuring data integrity across the healthcare system.
You will contribute to financial and business objectives by monitoring and analyzing budgets and resource data for a project portfolio. You will also collaborate cross-functionally to oversee financial aspects of projects and prepare estimates for contract modifications.
The Clinical Project Manager leads clinical study operations, including strategic planning, budget oversight, and site management from inception to completion. They are responsible for managing and motivating the study team while ensuring compliance with GCP, regulatory requirements, and project-specific plans.
The Inside Sales Specialist will focus on lead generation and prospecting by making high-volume calls to pharmaceutical and healthcare decision-makers. They will also manage the sales pipeline, set qualified appointments for the outside sales team, and maintain accurate records in the CRM.
The Associate Business Development Director is responsible for prospecting, qualifying, and closing new business opportunities within medical specialty societies. This role involves developing comprehensive sales plans, managing the full sales cycle, and serving as a liaison between customers and internal technical teams.
The IT Support Services Manager oversees daily Service Desk operations, endpoint management, and vendor relationships to ensure high-quality service delivery. They lead a team of support personnel while driving continuous improvement, automation, and compliance with regulatory standards.
The IT Support Services Manager oversees daily Service Desk operations, endpoint management, and vendor relationships to ensure high-quality IT support. They are responsible for driving continuous improvement, managing IT support personnel, and ensuring compliance with security and regulatory standards.
The Patient Recruiter acts as the primary contact for potential study participants, managing recruitment, education, and pre-screening processes. They are responsible for maintaining accurate patient records, scheduling study visits, and collaborating with clinical research teams to ensure study success.
The Project Operations Analyst coordinates clinical project activities, ensuring adherence to timelines, quality standards, and performance metrics. They also support project planning, milestone tracking, vendor oversight, and data quality management to ensure successful project delivery.
The General Manager will lead the strategy, performance, and growth of a significant Functional Service Provider (FSP) customer account. They are responsible for ensuring operational excellence, financial profitability, and strengthening executive-level client relationships.
You will manage day-to-day site start-up and activation activities while providing guidance and mentoring to the FSP Site Start Up team. Additionally, you will partner with Clinical Operations teams to improve study start-up metrics and ensure adherence to project timelines.
The Site Activation Lead designs and executes study start-up plans to ensure clinical trials move from planning to reality without delays. They oversee regulatory submissions, site contracts, and budget negotiations while leading cross-functional teams to maintain performance and data accuracy.
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The Therapeutic Strategy Director leads cross-functional teams to design innovative, data-driven solutions for CVRM programs to secure new business. They act as a strategic expert throughout the project lifecycle, ensuring client-centric proposals and effective delivery strategies.
Process and assess safety data and adverse events in accordance with regulatory requirements and internal SOPs. Collaborate with functional team members and healthcare professionals to ensure accurate reporting and project compliance.
The Medical Director serves as the medical lead for clinical trials in immunology, overseeing study execution and scientific risk. They are responsible for developing clinical protocols, managing clinical teams, and collaborating with key opinion leaders to ensure regulatory compliance.
The Senior Director is responsible for executing patient services strategy and overseeing the performance of call center programs for pharmaceutical and medical device clients. They will lead leadership teams, manage client relationships, and ensure operational excellence to meet revenue and profit targets.
The Senior Manager, Clinical Trial Liaison is responsible for site-facing engagement, operational support, and risk mitigation to ensure successful study execution. This role involves building strong relationships with investigative sites, overseeing CRO performance, and collaborating with cross-functional teams to drive recruitment and data quality.
The Clinical Research Associate will conduct site monitoring activities, including qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. They will also collaborate with site staff and investigators to maintain high-quality clinical data and prepare essential study documentation.
The Senior Pharmacovigilance Associate manages adverse event reporting, signal detection, and the preparation of regulatory documents like PSURs. They also oversee database integrity, provide mentorship to junior staff, and ensure compliance during regulatory audits.
The Senior Medical Writer will author, review, and manage clinical and regulatory documents to support global drug development programs. They will also coordinate cross-functional reviews and serve as the primary medical writing representative on project teams.
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The Medical Advisor will lead pre-launch medical affairs strategy and establish scientific relationships with key opinion leaders across the UK. They will provide medical oversight to cross-functional teams and support clinical research activities to ensure scientific integrity and alignment with global objectives.
The Clinical Trial Associate manages the delivery of the Rater Training Program by acting as a liaison between internal scientific teams, site staff, and study sponsors. They are responsible for maintaining study records, overseeing project deliverables, and providing operational support throughout the clinical trial lifecycle.
Collaborate on the design of clinical research studies and develop biostatistical analysis plans for research proposals and grants. Manage, analyze, and interpret study data while educating research team members on statistical methods.
The role is responsible for driving operational excellence and process optimization within the Program and Study Management function. It involves leading strategic initiatives, managing cross-functional collaborations, and ensuring clinical studies are executed efficiently and in compliance with regulatory standards.
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