Draft, review, and negotiate clinical site agreements and related documents to ensure compliance with regulatory standards.
Manage the full contract execution process, including tracking timelines, resolving issues, and coordinating signatures.
Act as a key liaison between internal teams and clinical sites, ensuring clear communication and adherence to budgets and regulations.
Our partner is a company in the life sciences industry focused on clinical trial execution and regulatory compliance, contributing to the development of life-changing therapies. The environment is collaborative, quality-driven, and fast-paced, with a strong emphasis on accuracy, communication, and professional growth.
Provide administrative and operational support to project teams throughout the clinical research project lifecycle.
Coordinate meeting logistics, documentation, and stakeholder communications to ensure smooth execution.
Assist with data entry, report generation, and compliance with regulatory requirements.
This partner company provides clinical research project management services to clients globally. They offer a fully remote, collaborative work environment focused on quality and continuous improvement.
Program and configure online market research surveys using Forsta Plus (ConfirmIT) to ensure accuracy and client satisfaction.
Collaborate with project managers and data processing teams to deploy seamless surveys and monitor fieldwork progress.
Conduct testing, troubleshoot issues, and propose design enhancements to improve data quality and respondent experience.
This partner company delivers market research and data collection services to global clients. It fosters a collaborative, remote culture with a focus on technical excellence and professional growth.
Own the end-to-end lifecycle of enrollment data, from inbound 834 file processing through system validation and data entry to ongoing maintenance.
Perform systematic data validation and quality assurance, identifying anomalies, duplicates, and discrepancies while executing scheduled and ad-hoc audits.
Lead targeted data cleanup projects and collaborate cross-functionally with engineering, claims, and population health teams to resolve data issues.
Evry Health is on a mission to bring humanity to health insurance, offering high-technology health plans that expand benefits and increase access. As the major medical division of Globe Life, it has 16.8 million policies in force and over 3,000 corporate employees and 15,000 agents, with a 45-year A (Excellent) rating from A.M. Best Company.
Review and update client data accurately based on provided Style Guides.
Research and validate information using internal and external data sources.
Resolve data discrepancies and merge duplicate records.
Harbor provides expert services in strategy, legal technology, operations, and intelligence. With a globally integrated team of over 900 strategists, technologists, and specialists, they serve leading law firms and corporations, fostering a culture of deep knowledge and mutual respect.
Independently prepare IRB documents, maintain regulatory files, and facilitate regulatory oversight of safety reporting for clinical trials.
Serve as the internal project manager for assigned oncology disease groups, providing timely updates and regulatory guidance.
Manage study activation processes and act as liaison between sponsors, investigators, and internal departments.
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. Winship Cancer Institute is Georgia's only NCI-designated Comprehensive Cancer Center, dedicated to discovering cures for cancer and providing innovative therapies.
Perform in-house and remote monitoring activities for clinical trials, ensuring compliance with regulatory requirements and study protocols.
Support study start-up, site selection, and document tracking while assisting CRAs with on-site and remote monitoring.
Communicate with investigative sites to resolve queries and maintain study tracking tools for deviations, SAEs, and data discrepancies.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. The environment is collaborative, international, and focused on improving patient outcomes through high-quality research.
Review inpatient and outpatient medical records to ensure accurate and compliant clinical documentation.
Collaborate with physicians and clinical teams to clarify diagnoses and support proper coding.
Maintain productivity targets and contribute to provider education initiatives to improve documentation quality.
Jobgether is an AI-powered job matching platform that connects candidates with hiring companies. It processes applications using AI to ensure fair review and shares top candidates with employers.
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of new medicines and treatments. As a values-driven company, ICON fosters a culture of integrity, collaboration, agility, and inclusion, employing a diverse workforce.
Configure Ironclad workflows, templates, and contract schemas based on solution designs.
Collaborate with Solution Architects and Project Managers to deliver CLM implementations.
Support client workshops, UAT, and technical integrations.
Consilio is the global leader in eDiscovery, document review, flexible legal talent, and legal advisory & transformation consulting services. The company empowers multinational law firms and corporations with innovative software and deep legal expertise, fostering a collaborative and high-performance culture.
Serve as system administrator and execution owner for all electronic GxP systems, maintaining validation and compliance throughout their lifecycle.
Configure, maintain, and troubleshoot system workflows, user roles, and security models in platforms like MasterControl and Veeva.
Support audits and inspections as a system subject matter expert, ensuring inspection-ready documentation and data integrity.
Kaléo is a global leader in drug‑delivery device technology and auto‑injector innovation. The company provides millions of patients, government partners, and emergency responders with security and peace of mind, operating as a focused, execution-driven organization.
Perform clinical validation and medical record abstraction to ensure accuracy and compliance with CMS quality measures.
Identify and resolve data discrepancies in collaboration with internal teams and external vendors like Oracle Health.
Support timely regulatory submissions and cross-train across validation and abstraction functions for workload flexibility.
Banner Health is a large, nonprofit health care system in the US, providing hospital services, primary care, and research across multiple communities. With a network of hospitals and clinics, they employ skilled professionals using advanced technology to improve patient care.