Coordinate project and programme management delivery for clinical trials, acting as the primary contact for sponsors. Manage 10-15 studies ensuring adherence to Good Clinical Practice and providing regular progress reports.
Remote Clinical Research Jobs (612)
Tags = clinical-research
The role involves providing administrative and operational support for clinical trials, including managing documentation and coordinating with cross-functional teams. Key duties include tracking trial progress, managing site communications, and ensuring regulatory compliance.
The Adjudication Project Manager is responsible for managing all endpoint adjudication processes for clinical trials in adherence to SOPs and regulations. This includes developing trial documentation, managing budgets and timelines, and leading internal processing teams.
Coordinate and perform remote clinical activities to collect and report patient data in compliance with study protocols and GCP. Manage virtual patient recruitment, enrollment, and informed consent processes while ensuring participant safety.
Lead the financial and operational oversight of clinical research billing and compliance for a community-based oncology program. Manage research finance analysts and coordinate with third-party providers to ensure accurate invoicing and regulatory adherence.
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Senior Specialist, Global Clinical Evaluation - MedTech Surgery
Johnson & Johnson Innovative Medicine
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Full Time
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2 Days Ago
Johnson & Johnson Innovative Medicine
The Senior Specialist serves as an operational excellence expert for clinical evaluation reports, systematic literature reviews, and medical writing across the MedTech Surgery business unit. They are responsible for optimizing processes, managing external vendors, and ensuring the timely delivery of high-quality regulatory documentation.
Principal Medical Writer (Publications)
Thermo Fisher Scientific
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Full Time
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2 Days Ago
Thermo Fisher Scientific
Lead the production of high-quality medical publications, abstracts, and posters from conception to completion. Act as the primary contact for clients and provide senior review, training, and mentorship to other writers.
The Global SSU Lead is responsible for the global execution of site activation for clinical trials, ensuring efficiency and compliance with SOPs and ICH/GCP. This includes developing start-up strategies, overseeing CRO performance, and managing regulatory documentation in the Trial Master File.
Lead the planning, execution, and delivery of clinical research projects while ensuring alignment with business objectives and ICH-GCP compliance. Direct project management activities, manage client relationships, and coach team members to achieve operational and financial metrics.
Lead the development of scientific and promotional medical communications, including manuscripts, posters, and slide decks. Partner with clients to create strategic narratives and ensure all content is scientifically accurate and compliant.
The Regulatory Analyst I prepares and maintains regulatory documentation for clinical trials from start-up through closure. This includes managing submissions to boards and committees, ensuring compliance with FDA and NIH regulations, and maintaining the Trial Master File.
The Regulatory Analyst prepares and maintains regulatory documentation for clinical trials from start-up through closure. This includes managing submissions to boards and committees, ensuring compliance with FDA and NIH regulations, and updating Trial Master Files.
Senior Manager Master Data Management
Blood Cancer United
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Full Time
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2 Days Ago
Blood Cancer United
The Senior Manager is responsible for the design, implementation, and daily operation of the master data program, ensuring a single trusted version of critical data records. This includes managing data domains, establishing golden record standards, and supervising a junior staff member.
The Accounts Receivable Team Lead manages the AR team, oversees invoicing and collections, and maintains KPIs for stakeholders. They are responsible for ensuring operational efficiency, accuracy in billing, and continuous improvement of AR processes.
Regulatory Support Specialist (Remote- India)
Monroe+Biomedical+Research
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Full Time
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2 Days Ago
Monroe+Biomedical+Research
The role involves preparing and submitting regulatory documents such as IRB submissions and maintaining audit-ready electronic regulatory files. The specialist will also support clinical study start-up activities and ensure compliance with FDA and ICH-GCP guidelines.
The role involves designing and executing clinical trial protocols, managing site selection, and overseeing data collection for Hematology and Hemostasis products. It also requires performing statistical analysis and authoring comprehensive final study reports for regulatory submission.
You will manage day-to-day project and program management activities, supporting your team to deliver quality outcomes. Key responsibilities include developing project plans, leading cross-functional teams, and collaborating with stakeholders.
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The Scheduler will manage patient onboarding and coordination within the Patient Support Programme, including processing referrals and creating patient records. They will also conduct welcome calls, allocate patients to nurses, and handle telephone queries.
The Scientific Advisor, Director leads biomarker strategies for translational and clinical studies and serves as the scientific lead for protein biomarker programs. This role involves engaging clients, translating complex technical concepts into practical study plans, and supporting business development efforts.
The Clinical Research Associate (CRA) oversees the quality and compliance of clinical trial sites, ensuring adherence to protocols and regulations. They conduct site visits, monitor data integrity, and maintain relationships with stakeholders.
Medical Science Liaison, Rheumatology - Western Canada
Johnson & Johnson Innovative Medicine
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Full Time
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2 Days Ago
Johnson & Johnson Innovative Medicine
The Medical Science Liaison (MSL) is responsible for executing the Medical Sciences Plan and serving as the scientific point of contact for key individuals in the territory. This includes building relationships with healthcare professionals, presenting scientific data, and supporting clinical development programs.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and industry standards. Lead monitoring tasks, conduct site visits, and provide guidance to site staff and other CRAs to maintain high quality standards.
Regulatory Affairs Specialist- Belgian Dutch speaker- Remote
Worldwide Clinical Trials
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Full Time
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2 Days Ago
Worldwide Clinical Trials
The role involves planning and submitting regulatory dossiers and coordinating with ethics committees to ensure clinical trial compliance. It also requires maintaining country-specific labeling and patient information while providing strategic regulatory advice.
Account Director/Sr Account Director, Business Development (Bioanalytical Labs) -MidAtlantic
Thermo Fisher Scientific
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Full Time
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2 Days Ago
Thermo Fisher Scientific
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage the full sales cycle from RFP strategy and proposal development to contract negotiation and client satisfaction.
Clinical Trial Manager II. Barcelona or Madrid. FSP
Syneos Health
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Full Time
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2 Days Ago
Syneos Health
Responsible for site management oversight, clinical monitoring, and ensuring patient safety and data integrity across clinical trials. The role involves managing CRAs, overseeing study deliverables, and collaborating with functional leaders to meet study milestones.
The CRA is responsible for the initiation, monitoring, and close-out of clinical study sites to ensure subject safety and data integrity. This includes verifying protocol compliance, reviewing source documentation, and preparing timely monitoring reports.
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The Senior Clinical Research Associate is responsible for the initiation, monitoring, and close-out of study sites to ensure subject safety and data integrity. They must maintain study documentation in accordance with GCP, ICH guidelines, and regulatory requirements while providing guidance to project teams.
Lead the end-to-end delivery of global clinical trials from start-up to close-out, ensuring compliance with ICH-GCP and company SOPs. Manage sponsor relationships, project budgets, and cross-functional teams to ensure studies are delivered on time and within budget.
Acts as the primary point of contact for clients regarding live eCOA studies and maintenance. Manages project scope, schedules, budgets, and leads system change efforts and client update meetings.
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards. This includes conducting site visits, collaborating with cross-functional teams, and providing guidance to site staff to ensure data integrity and participant safety.
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