Gather, analyze, and document business, technical, and clinical requirements for AI-driven patient health data summarization, including user stories, process flows, and acceptance criteria.
Analyze C-CDA clinical documents and map clinical information to healthcare interoperability standards, ensuring traceability and data quality.
Collaborate with clinicians, data scientists, and engineers in Agile ceremonies to validate AI-generated clinical summaries and support User Acceptance Testing.
VetsEZ supports large federal government healthcare modernization projects, including AI-driven clinical decision support. The company fosters a collaborative, Agile culture with multidisciplinary teams focused on delivering quality healthcare IT solutions.
Evaluate RFPs and contribute to bid strategies for clinical supply proposals.
Collaborate with business development, contracts, proposals, and operations teams to align budgets and assumptions.
Manage multiple priorities in a fast-paced international environment while maintaining quality and accuracy.
This partner company operates in the clinical research and supply chain environment, supporting high-quality proposals and clinical trial supply management. It provides a fully remote, supportive working environment with a focus on employee health and wellbeing, offering exposure to international projects and collaboration with cross-functional teams.
Develop and deliver training on clinical and operational workflows within electronic health records, focusing on WellSky.
Create training materials and documentation to support end-user adoption and regulatory compliance.
Perform business analysis by gathering requirements, mapping workflows, and identifying gaps to improve system use.
PAM Health provides specialty healthcare services through more than 80 locations across 17 states, including wound clinics and outpatient physical therapy. The company fosters a collaborative environment with opportunities for professional growth, competitive pay, and generous benefits.
Support clinical trial activities across patient engagement, study coordination, recruitment, regulatory support, data management, and operations.
Coordinate participant visits, recruitment, and regulatory documentation while maintaining accurate information in clinical research systems.
Foster communication between sponsors, CROs, investigators, and sites to ensure study compliance and milestone achievement.
This partner company supports fast-growing remote clinical research environments, helping keep clinical trials organized, compliant, and moving forward. They collaborate with research sites, sponsors, CROs, and healthcare organizations globally, offering multidisciplinary roles in a remote setting.
Assess clinical information needs and refine clinical processes to improve safety and efficiency at the point of care.
Analyze and document clinical workflows using BPM+ notation and drive enterprise workflow standardization.
Develop, implement, and continuously refine clinical decision support and clinical content in the federal EHR.
Aptive partners with federal agencies to achieve their missions through improved performance, streamlined operations and enhanced service delivery. Founded in 2012, the company has over 300 employees nationwide and focuses on applying technology and human-centered services to optimize government mission delivery.
Ensure quality and completeness of medical record documentation through concurrent interaction with physicians and staff.
Facilitate modifications to clinical documentation to support accurate reimbursement and severity capture for inpatients.
Educate patient care team members on documentation best practices and support timely, accurate reporting.
Cooper University Health Care is a healthcare organization dedicated to providing extraordinary care through clinical innovation and advanced facilities. It offers a comprehensive benefits program and opportunities for career growth, with a team-oriented culture.
Develop and maintain clinical data listings, reports, and programming solutions to support data review and safety monitoring.
Analyze requirements from Data Management and Risk-Based Study Management teams and create efficient programming solutions.
Ensure all activities comply with regulatory requirements, industry guidelines, and internal procedures.
A partner company in the clinical research industry supports global clinical research programs through data analysis and programming. The company offers a fully remote, collaborative environment with a focus on continuous learning and improvement.
Manage day-to-day operations for the outpatient clinical documentation improvement program across multiple facilities.
Liaise with physicians and leadership on coding rules, risk adjustment, and reimbursement guidelines.
Ensure compliant and accurate medical record documentation while facilitating standardization.
Henry Ford Health is an academic health system providing comprehensive care across Michigan. With 12 hospitals and hundreds of clinics, it is a large organization focused on collaboration and innovation.
Act as a link between business stakeholders and technical teams to translate requirements into practical solutions.
Analyze business needs and document system requirements to support digital strategies.
Build expertise in client industries and take increasing ownership of projects.
The company is a technology consulting firm that helps clients solve strategic business problems. It operates with a fully remote team and emphasizes collaboration and professional growth.
Plan, lead, and oversee projects using project management processes to meet deadlines and budgeted costs.
Analyze and research business problems, design innovative solutions, and develop/maintain programs for the clinical data repository.
Collaborate with customers and IT, conduct tests, and provide off-hours support to ensure quality and service.
Capital Blue Cross is a health insurance company and independent licensee of the Blue Cross Blue Shield Association. They provide health insurance plans and services to members in Pennsylvania and are an equal opportunity employer.
Serves as regulatory document specialist for clinical trial start-up, maintenance, and close-out.
Collects, reviews, and maintains essential documents in the electronic Trial Master File (eTMF).
Communicates with study teams and sites to ensure regulatory files remain complete and inspection-ready.
St. Jude Children’s Research Hospital is a leading research and treatment center focused on pediatric catastrophic diseases. It is a large institution with a collaborative culture and a strong emphasis on finding cures and saving children.
Critically evaluate scientific literature and produce accurate regulatory documents.
Manage writing assignments across multiple projects and ensure timely delivery.
Work directly with clients and multidisciplinary teams on regulatory submissions.
A partner company in the pharmaceutical, biotechnology, and medical device sectors is hiring a Senior Medical Writer. The company offers a fully remote environment and opportunities to work on a broad portfolio of clinical and regulatory documents.
Coordinate day-to-day execution of clinical studies including site onboarding, documentation, and timeline tracking.
Support regulatory compliance through IRB submissions, amendments, and maintaining study documentation.
Collaborate cross-functionally with science, bioinformatics, and product teams to ensure study operations.
Tiny Health advances lifelong health through precision microbiome science using shotgun metagenomics and AI. Founded in 2020, it is a remote-first startup with a diverse international team focused on making the microbiome measurable and actionable.
Apply specialized clinical knowledge to categorize, code, and interpret registry data from patient medical records.
Ensure quality submission of data in specified registries, maintaining high accuracy standards.
Prioritize tasks, meet tight deadlines, and troubleshoot technical issues with EMR systems.
Q-Centrix partners with hospitals to deliver quality clinical data solutions, specializing in cancer registry and data abstraction. With a remote-first culture and employee-centric leadership, the company has earned the Great Place to Work distinction multiple years.
Own use case deployments end-to-end from contract signature to go-live, driving accountability to timeline and quality.
Build Implementation Charters, configure platform settings, and coordinate with health system IT teams for seamless integration.
Define and refine the standard onboarding process for providers, creating reusable playbooks for scalable deployments.
Hippocratic AI is building the world's first healthcare-only, safety-focused large language model platform to transform patient outcomes. The company is backed by leading investors and co-founded by a team of physicians and AI pioneers, with over $400 million in funding.
Lead clinical data risk management and central monitoring across multiple clinical studies.
Evaluate clinical trial data to identify risks, trends, and emerging issues affecting study outcomes.
Develop key risk indicators and analytical approaches to support risk-based quality management.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. They operate globally but focus on efficient and fair candidate review processes.
Lead the implementation and adoption of new technologies, systems, and business processes that support feasibility, patient engagement, and site solutions.
Collaborate with internal stakeholders, functional experts, technical teams, and external vendors to deliver successful technology implementations.
Develop, organize, and maintain training materials, process documentation, performance metrics, and proposal-ready capability resources.
Our partner is a clinical research organization that enables patient and site solutions through technology and process improvements. They offer a collaborative, inclusive, and globally connected work environment that supports professional growth and innovation.
Lead the preparation of complex clinical and regulatory documents including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures.
Collaborate with clinical development teams and stakeholders to produce accurate, compliant, and scientifically robust documentation.
Manage document timelines, review cycles, and project deliverables while ensuring quality standards and regulatory requirements are met.
Our partner is a specialized medical writing team supporting the development of high-quality regulatory documentation for the global pharmaceutical industry. It offers a collaborative, remote environment focused on quality, precision, and scientific communication.