The Senior Statistical Programmer is responsible for reviewing datasets and ensuring submission readiness of clinical data. They will collaborate with study teams to design data structures and oversee the development of SAS programs for clinical data analysis.
Remote Clinical Research Jobs (607)
Tags = clinical-research
Lead and manage the strategic, operational, and financial delivery of Site Activation activities across assigned studies and regions. Oversee regulatory submissions, approvals, contracts, and essential document processes to ensure timely patient enrollment.
Manage Medical Information staff and support operational decisions as directed by senior management. Collaborate with stakeholders to achieve local and global deliverables and metrics.
Cardiac Rhythm Management Technical Field Engineer -Palm Beach
Medtronic
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Full Time
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3 Days Ago
Medtronic
The role involves leading regional customer and employee education and training activities for Cardiac Rhythm Management procedures and product launches. The engineer will also serve as a technical resource, providing expertise and support to improve district and region performance.
Sr. Clinical Research Coordinator
Mass General Brigham
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Full Time
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3 Days Ago
Mass General Brigham
The Sr. Clinical Research Coordinator will coordinate and administer clinical research projects, enrolling eligible patients and managing data collection. They will also serve as a liaison between the clinical team, sponsor, and Institutional Review Board to ensure effective communication.
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Medical Science Liaison, Cell Therapy Autoimmune (CTAI) - (NM, N. TX, OK)
Bristol Myers Squibb
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Full Time
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3 Days Ago
Bristol Myers Squibb
Develop and maintain professional relationships with medical thought leaders to provide scientific support for Cell Therapy Autoimmune products. Collaborate with internal teams to enhance clinical trial enrollment and provide medical information through fair-balanced scientific exchange.
The analyst is responsible for delivering high-quality eCOA solution designs by translating pharmaceutical client requirements and study protocols into optimized specifications. They coordinate the design process and collaborate with cross-functional teams to ensure data integrity and efficient project delivery.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc
Fortrea
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Full Time
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3 Days Ago
Fortrea
Responsible for all aspects of clinical site monitoring, including initiation, routine visits, and close-out of oncology trials. Ensures data integrity, patient safety, and adherence to study protocols and regulatory requirements.
FSP Principal Medical Writer (Regulatory) - Client-Dedicated
Thermo Fisher Scientific
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Full Time
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3 Days Ago
Thermo Fisher Scientific
Lead the planning, writing, and delivery of high-quality clinical and regulatory documents such as CSRs, protocols, and IBs. Provide subject matter expertise on document strategy and mentor junior medical writers to ensure operational excellence.
Lead Medical Project Coord
Thermo Fisher Scientific
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Full Time
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3 Days Ago
Thermo Fisher Scientific
Lead the management and coordination of medical projects to ensure compliance and optimal performance throughout the project lifecycle. Perform safety data reviews, manage project financials, and serve as the primary point of contact for clinical project teams.
Medical Project Coordinator
Thermo Fisher Scientific
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Full Time
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3 Days Ago
Thermo Fisher Scientific
Coordinate and review safety data to ensure compliance with regulatory standards and optimal patient safety in clinical trials. Identify safety trends, resolve complex issues, and support the creation of safety and medical management plans.
Senior Medical Project Coordinator
Thermo Fisher Scientific
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Full Time
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3 Days Ago
Thermo Fisher Scientific
The Senior Medical Project Coordinator manages and evaluates medical projects to ensure compliance, alignment, and optimal performance throughout the project lifecycle. This includes reviewing safety data, managing project financials, and serving as the primary point of contact for clinical project teams.
The Medical Director will provide strategic input into clinical projects and manage medical monitoring for clinical trials. Responsibilities include supporting site investigators and addressing queries related to inclusion/exclusion criteria.
Clinical Trial Manager with at least 5 years of experience in clinical research and experience as a CTM working with US - Mexico Home Based
Syneos Health
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Full Time
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3 Days Ago
Syneos Health
The role involves managing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires overseeing data integrity, investigational product reconciliation, and maintaining the Trial Master File.
The Coder Inpatient reviews medical records and performs coding on all diagnoses and procedures. They are responsible for maintaining the confidentiality of patient records while ensuring compliance with coding guidelines and regulations.
VP Strategic Advisory Partnerships
Omega Healthcare Solutions
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Full Time
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3 Days Ago
Omega Healthcare Solutions
The VP Strategic Advisory Partnerships will position Omega as a partner of choice within the advisory ecosystem and drive measurable revenue through influenced and co-developed sales opportunities. Responsibilities include developing relationships with advisory firms, identifying opportunities for collaboration, and enabling revenue generation through strategic partnerships.
The Senior Specialist, Regulatory Operations will oversee and execute all site-level regulatory operational activities for assigned clinical trials in the U.S. This role includes ensuring compliance with applicable U.S. regulations and guidelines and supporting regulatory activities for Canadian sites as needed.
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Manager, Global Clinical Monitoring
Precision Medicine Group
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Full Time
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3 Days Ago
Precision Medicine Group
Responsible for the line management, performance, and development of CRAs, IHCRAs, and CTMs across multiple European countries. The role also involves driving operational excellence initiatives and ensuring high-quality execution of clinical operations activities.
Manager, Global Clinical Monitoring
Precision for Medicine
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Full Time
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3 Days Ago
Precision for Medicine
Responsible for the line management, performance, and development of CRAs, IHCRAs, and CTMs across European regions. The role involves optimizing clinical operations performance and leading departmental initiatives for operational excellence and process improvement.
Director, Clinical Scientist (Respiratory indications)
Generate Biomedicines
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Full Time
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3 Days Ago
Generate Biomedicines
Lead clinical science for Phase 2 and 3 respiratory trials, focusing on asthma and COPD. Drive the development of protocols, regulatory documents, and oversee day-to-day study execution and data quality.
Monitor the collection and analysis of data from third-party suppliers for sponsored clinical trials. Evaluate supplier compliance, track corrective actions, and maintain professional relationships with external stakeholders.
The Attorney 1 will prepare SEC filings and provide counsel on compliance, governance, and capital markets transactions. They will also manage legal entity reorganizations and coordinate sustainability reporting requirements.
Provide remote second-tier IT support to resolve end-user operating difficulties and identify core system problems. Escalate complex issues to management and provide guidance to less experienced Service Desk staff.
The Associate Director of Clinical Affairs is responsible for creating and executing clinical strategies, including the design and support of clinical studies and protocol development. This role involves overseeing CROs and collaborating with cross-functional teams to facilitate trial enrollment and regulatory compliance.
Manage clinical trial projects from start-up through closeout, ensuring adherence to timelines, budgets, and regulatory requirements. Serve as the primary liaison between sponsors, internal teams, and vendors while leading project planning and execution.
Manage clinical trial operations, including budget oversight, study start-up, and enrollment activities. Coordinate with sponsors and vendors while mentoring Clinical Research Associates to ensure high-quality study outcomes.
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The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. They ensure protocol compliance and data integrity while collaborating with investigators to maintain high-quality clinical data.
Lead site start-up and activation tasks, including feasibility assessments, contract negotiations, and regulatory submissions. Ensure patient welfare by reviewing informed consent forms and maintaining high standards of regulatory compliance.
The role involves reviewing RFPs to develop strategic proposals, budgets, and scopes of work for customers. It also requires coordinating with internal stakeholders to ensure document quality and maintaining corporate tracking databases.
Lead the vision, strategy, and growth of a new digital community and engagement platform for healthcare professionals. Collaborate cross-functionally to translate customer needs into innovative solutions and drive long-term user adoption and retention.
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