Director, Business Development
Drive revenue growth by securing new clients and expanding services for global clinical operations. Manage the full sales lifecycle from prospecting and relationship building to closing complex, high-value deals.
Remote Clinical Research Jobs (2,317)
Senior Site Contract Associate - IQVIA Biotech
Manage start-up contracting activities, including developing investigator grant estimates and maintaining contract templates for biotech sponsors. Ensure compliance with regulatory requirements and project timelines while collaborating with stakeholders and RSU regions.
Principal Statistical Programmer
The Principal Statistical Programmer leads clinical sub-teams by delegating tasks, providing technical support, and ensuring the accuracy of SAS code and output. They are responsible for creating necessary files and analyses for electronic submissions in eCTD format while ensuring compliance with FDA/ICH/GCP regulations.
Senior Clinical Research Associate (Level I)
The Senior CRA coordinates clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory requirements. Responsibilities include conducting remote or on-site visits, managing documentation, and maintaining collaborative relationships with investigational sites.
Clinical Research Financial Analyst II
Develop, coordinate, and negotiate financial budgets for NIH and pharmaceutical sponsored clinical research trials. Resolve issues related to billing, milestones, and payments while serving as a budgeting resource for clinical projects.
Be the one who applies first
We watch for new remote clinical research jobs and email you the matches. Free. Unsubscribe in one click.
Sr. CRA 2, FSP - Invitro Diagnostics
Responsible for all aspects of study site monitoring, including routine monitoring, close-out visits, and site management. Ensures the protection of study participants and the integrity of clinical trial data through rigorous verification and reporting.
Medical Director/Sr Medical Director - Pulmonary
Provide medical oversight for clinical trials to ensure compliance with SOPs, GCP, and regulatory requirements. Perform medical review of safety data, adverse events, and clinical trial deliverables such as CSRs and periodic safety reports.
Senior Account Executive
The Senior Account Executive is responsible for fostering client relationships and managing the end-to-end sales process to drive revenue growth. They collaborate with cross-functional teams to deliver high-quality services and monitor account performance to ensure client satisfaction.
CRA II / Sr CRA
Responsible for site management and monitoring of clinical trials, including conducting initiation, routine, and close-out visits. Ensures data integrity, subject protection, and adherence to ICH GCP guidelines and sponsor requirements.
Digital Experience & Web Development Specialist
Develop and maintain professional websites for Health Haven and Health Synergy Clinical Research to improve user experience and digital presence. Manage SEO, content updates, technical security, and integrations with business systems to drive patient and participant enrollment.
AI & Business Automation Specialist
The specialist will design and implement AI solutions and automated workflows to improve operational efficiency across clinical and administrative departments. They will also manage systems integrations, create business intelligence dashboards, and lead technology projects from concept to implementation.
AI & Business Automation Specialist
The specialist will design and implement AI solutions and automated workflows to improve operational efficiency across clinical and administrative departments. They will also manage systems integrations, create business intelligence dashboards, and lead technology projects from concept to implementation.
Digital Experience & Web Development Specialist
Develop and maintain professional websites for Health Haven and Health Synergy Clinical Research to enhance digital presence and user experience. Optimize website performance, SEO, and conversion pathways while managing integrations with business systems and ensuring brand consistency.
Site Engagement Manager
Act as a communication bridge between clinical sites, vendors, and sponsors to remove enrollment barriers and enhance study performance. Build strong relationships with principal investigators and site staff while monitoring performance metrics and implementing engagement strategies.
Clinical Project Manager / Senior Clinical Project Manager
Lead full-service clinical trials in Oncology, overseeing functional departments to ensure timelines, scope, cost, and quality are met. Act as the primary client liaison and manage the full study lifecycle from proposal and bid defense to completion.
Clinical Project Manager / Senior Clinical Project Manager
Lead and oversee full-service global clinical trials in Oncology, managing timelines, scope, cost, and quality. Act as the primary client liaison and coordinate cross-functional teams across data management, safety, and biostatistics.
Clinical Trial Manager
Manage day-to-day clinical trial operations, ensuring adherence to timelines, budgets, and quality standards. Collaborate with cross-functional teams and investigators to implement protocols and ensure regulatory compliance.
Be the one who applies first
We watch for new remote clinical research jobs and email you the matches. Free. Unsubscribe in one click.
Senior Director, Clinical Development
The Senior Director will provide clinical science leadership, managing the design, planning, and execution of clinical trial programs with minimal guidance, and leading study design, implementation, and execution for assigned programs. This role involves serving as a major contributor to protocols, data interpretation, final reports, and overseeing medical monitoring activities for all human clinical trials.
Clinical Research Associate / Senior Clinical Research Associate
The Clinical Research Associate will conduct and report all types of onsite and remote monitoring visits, perform CRF review, source document verification, and manage site communication. Responsibilities also include involvement in site identification and potentially assisting in training less experienced CRAs.
UN
Clinical Research Specialist II
The interventionist will conduct Cognitive Behavioral Therapy for Treatment-Seeking with Deaf Individuals (Deaf CBT-TS) intervention sessions remotely via Zoom with Deaf participants, ensuring participant well-being and adherence to ethical principles. Responsibilities also include coordinating scheduling, managing participant inquiries, recording session notes, and following up with written action plans and resources.
UN
Clinical Research Specialist II
The interventionist will conduct Cognitive Behavioral Therapy for Treatment-Seeking with Deaf Individuals (Deaf CBT-TS) intervention sessions remotely via Zoom with Deaf participants, ensuring participant well-being and adherence to protocol. This includes coordinating scheduling, maintaining rapport, recording sessions, and following up with resources and action plans.
Senior Manager, Clinical Partner Outsourcing
The Senior Manager, Clinical Partner Outsourcing ensures seamless execution of clinical studies by developing robust supplier contracts through commercial negotiations and resolving commercial and operational challenges. This role is responsible for maintaining fiscal discipline, enhancing cross-functional collaboration, and ensuring studies start on time aligned with business requirements and Takeda standards.
Business Development-Clinical Trials 13 applicants
The specialist will be responsible for identifying and engaging potential clients such as medical practices, hospitals, and research centers to expand the clinical trials network. This includes building strong relationships with decision-makers and developing strategic sales plans to drive growth.
Site Management Associate
The Site Management Associate I will assist in monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP guidelines. This role involves supporting site management activities such as documentation, data entry, tracking performance metrics, and collaborating with teams to resolve site-related issues.
CRA single-sponsor in Germany
The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will assess site performance, manage site-level activities, and support patient recruitment and retention strategies.
Medical Director/Clinical Trial Physician(Rheumatology)
Provide medical leadership to study teams and ensure the medical validity of clinical studies. Contribute to the creation and review of clinical trial protocols and ensure compliance with medical aspects.
Be the one who applies first
We watch for new remote clinical research jobs and email you the matches. Free. Unsubscribe in one click.
Principal CRA – Lead Monitor (m/w/d)
The Principal CRA will lead and coordinate all aspects of clinical monitoring and site management for complex trials, ensuring adherence to protocols, ICH-GCP, and regulatory requirements while acting as a subject-matter expert and escalation point. Key duties involve leading monitoring activities, performing site visits, overseeing data review, managing essential documents, and driving corrective actions.
Senior Clinical Informatics Sales Specialist, Pacific
The Senior Clinical Informatics Sales Specialist will drive customer adoption and sales growth of Informatics products by providing technical guidance and expertise. They will consult with customers on informatics requirements and develop presentations to facilitate sales.
Clinical Trial Manager(Sr.) - All Level
The Clinical Trial Manager will oversee the planning, execution, and successful completion of clinical trials while ensuring adherence to timelines, budgets, and regulatory guidelines. This role involves collaborating with cross-functional teams and managing site relationships to drive successful clinical trial outcomes.
Clinical Research Associate II
As a Clinical Research Associate, you will act as the main line of communication between the project team, sponsor, and site while ensuring quality standards in clinical studies. You will prepare and conduct monitoring visits, manage subject recruitment, and ensure compliance with study protocols.
Automatically Apply to the Best Remote Jobs
Stop the endless job search. Our AI finds and applies to the best jobs for you.
Browse Jobs by Role
Remote Data Analyst Jobs
Remote Management Consultant Jobs
Remote Account Executive Jobs
Remote Call Center Representative Jobs
Remote Graphic Designer Jobs
Remote Social Media Manager Jobs
Remote Proofreader Jobs
Remote Program Manager Jobs
Remote Video Editor Jobs
Remote Translator Jobs
Remote Technical Writer Jobs
Remote Customer Success Manager Jobs
Remote Software Engineer Jobs
Remote Content Creator Jobs
Remote Chief of Staff Jobs