Monitor real-time statuses of clinical research assets and respond to system alerts to ensure operational reliability. Coordinate with field personnel and internal stakeholders to resolve equipment issues and maintain accurate documentation for compliance.
Care Access
34 Remote Job Openings at Care Access
The Central Study Coordinator manages patient education, retention, and pre-screening for clinical research programs. Key duties include explaining lab results, conducting virtual informed consent processes, and matching participants to appropriate study protocols.
Drive scalable improvements across Clinical Delivery teams by translating enterprise priorities into practical operational workflows. Lead strategic initiatives focused on referral optimization, staffing support, and end-to-end process redesign to enhance efficiency and quality.
The role focuses on developing and executing engagement and retention strategies for patients through health screenings and studies. Key duties include optimizing the patient journey, building automation workflows, and implementing segmentation to improve participation rates.
The Senior Media Specialist manages campaign activation and optimization for health screening programs using traditional and localized media channels. They are responsible for identifying growth channels, managing vendor relationships, and collaborating cross-functionally to drive data-backed marketing solutions.
Lead the development and execution of data-driven digital campaigns to increase patient engagement and recruitment. Manage multi-million dollar budgets across paid search, social, and programmatic channels while optimizing performance through analytics.
The CTMS Operations Manager oversees platform governance, technical support, and operational reporting while leading the CTMS operations team. They serve as the final gatekeeper for site and study builds, ensuring GxP compliance and continuous process improvement.
Develop dashboards and analytical reports to monitor and improve organizational performance and quality standards. Collaborate with cross-functional leaders to identify performance levers and provide data-driven insights for decision-making.
Build and strengthen partnerships with Trial Access Partners to enhance clinical trial access for patients. Act as a liaison between partners and internal stakeholders while managing physician engagement and sales quotas.
Manage the end-to-end post-production process for long-form and short-form video content, from raw media ingestion to final delivery. Shape compelling narratives through precise pacing, color grading, and audio mastering to impact audiences across various platforms.
The Clinical Vendor Activation Manager oversees vendor engagement during clinical trial start-up, ensuring vendors are qualified, contracted, and aligned with study protocols. They act as a clinical point-of-contact to troubleshoot issues, monitor performance, and manage vendor relationships throughout the contract lifecycle.
The Manager, Quality Assurance drives quality management system activities including auditing, inspection readiness, and CAPA management. This role partners across the organization to ensure patient safety, data integrity, and regulatory compliance in clinical research.
The CTMS Operations Analyst is responsible for executing CTMS site and study build configurations, performing quality control, and providing technical support to users. They also produce operational reports and dashboards to support study readiness and platform governance.
The CTMS Operations Analyst is responsible for executing CTMS site and study build configurations, performing quality control, and providing technical support to users. They also produce operational reports and dashboards to support study readiness and platform governance.
The Senior Trainer will lead the development and delivery of onboarding, upskilling, and competency programs for clinical staff and investigators. They will collaborate cross-functionally to ensure training initiatives align with regulatory standards, operational goals, and quality performance metrics.
The Source Document Specialist is responsible for preparing and maintaining accurate, compliant clinical trial documentation while ensuring alignment with study protocols. They manage version control, coordinate with site staff, and implement process improvements to support global clinical research operations.
The role involves managing HR administrative tasks such as payroll, compliance, and onboarding while simultaneously driving talent acquisition efforts. You will support international operations, specifically focusing on Poland and the UK, to ensure smooth HR processes and effective recruitment.
The role involves supporting recruitment and HR administrative functions, including payroll, onboarding, and compliance for international locations. You will also manage candidate sourcing, screening, and interview coordination to support team growth.
The Senior Accountant will oversee daily accounting activities, manage the general ledger, and ensure accurate month-end closing processes. They will also lead revenue recognition determinations, coordinate external audits, and drive process improvement initiatives.
Manage the end-to-end planning, coordination, and execution of live events and film productions from concept through post-production. Oversee budgets, vendor negotiations, logistics, and on-site operations while ensuring adherence to safety and brand standards.
The Senior Specialist oversees and executes site-level regulatory operational activities for clinical trials to ensure compliance with FDA and global standards. They provide regulatory guidance to site teams, manage IRB submissions, and maintain essential study documentation throughout the trial lifecycle.
The manager is responsible for the identification, sourcing, qualification, and negotiation of clinical vendor relationships to support study objectives. They will also monitor vendor performance against SLAs and KPIs while ensuring cost-effective procurement and contractual compliance.
The Director of Financial Operations oversees and optimizes financial processes, including Accounts Payable, Accounts Receivable, and Revenue Operations. This role involves driving efficiency, managing financial systems, and collaborating with cross-functional teams to align financial processes with business objectives.
The Central Study Coordinator β Retention manages retention work for assigned participants, focusing on delivering a high-quality customer experience by educating, retaining, and considering them for study participation. This involves sharing lab results, conducting virtual consenting, and pre-screening participants for specific clinical studies.
The Growth Marketing Manager will own and execute the SEO strategy, including technical SEO and on-page optimizations, while also conducting site audits to enhance organic search rankings and user engagement. This role involves collaborating with developers to optimize the digital user experience, tracking website performance metrics, and managing analytics tools.
The Registered Nurse will manage the communication of critical and abnormal lab results to patients, ensuring compliance with state licensure requirements, and will also serve as a point of escalation for complex inquiries from the Member Services team. This role involves patient education regarding lab results and collaborating with providers to ensure all patient interactions are appropriately managed and documented.
The specialist will oversee day-to-day accounting activities, monitor the general ledger for accurate month-end close, and lead ASC 606 revenue determinations and accounting treatments. They will also collaborate on revenue recognition policies, assist with external audits and tax filings, and develop accounting documentation.
The Senior Business Development Director will drive business growth for Care Access by creating customized solutions for customers and study protocols, leveraging knowledge of the Global Site Network. This role involves managing key account relationships, owning strategic growth plans, and navigating the sales process to ensure successful outcomes with pharmaceutical, biotech, medical device Sponsors, and CROs.
The Contracts Manager will draft, review, and negotiate a variety of contracts while ensuring compliance with legal and regulatory requirements. They will also serve as the primary point of contact for contract-related inquiries and maintain a centralized contract repository.
The Senior Data Engineer will design, develop, and maintain data pipelines for reliable data ingestion and transformation. This role involves collaboration with cross-functional teams to deliver data solutions that meet clinical, operational, and business needs.
Associate Director, Patient Recruitment Partnerships
Care Access
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Full Time
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5 months ago
Care Access
The Associate Director, Patient Recruitment Partnerships leads the strategy for building and optimizing a high-performing ecosystem of Recruitment Vendors and Patient Advocacy Organizations. This role involves identifying, contracting, and evaluating partners to ensure high-quality patient referrals that accelerate enrollment across clinical trials.
The Site Support Solutions Manager will oversee the daily operations of the SSS team, ensuring high performance and exceptional customer experience. They will collaborate with sponsor teams and Care Access leadership to set priorities and translate them into actionable goals for the team.
The Enterprise Performance Analytics Engineer will support the development and maintenance of analytics infrastructure, focusing on building and maintaining foundational data models and ensuring data quality. This role involves collaborating with data analysts and stakeholders to understand data needs and implement models that support reporting and analysis.
The Registered Dietitian provides remote study support by assessing nutritional needs and promoting healthy physical activity. They deliver personalized Lifestyle Counseling to optimize nutritional status during pharmacotherapy.