Act as primary representative for eClinical Solutions and sponsor data management interaction, ensuring quality and timelines within scope.
Define specifications and collaborate with technical teams on configuration of elluminate for data cleaning strategy and oversight.
Perform quality oversight and data trending via elluminate reporting to identify risks and develop mitigation strategies.
eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. The company is a people-first organization with an inclusive culture, recognized as a 2025 Top Workplaces USA Award winner for Remote Work.
Provide data management support for clinical trials from start-up to post-database lock under supervision.
Assist in developing CRF specifications, building and testing clinical databases, and conducting user acceptance testing.
Review and query clinical trial data, perform medical coding, and coordinate with sponsors and vendors.
Precision for Medicine is a global precision medicine clinical research services organization that improves clinical research and development for new therapeutics. They integrate clinical operations, laboratory expertise, and data sciences, with a focus on oncology and rare disease.
Oversee clinical data management activities across complex research studies from start-up to database lock.
Act as primary data management subject matter expert and client-facing representative.
Lead cross-functional collaboration with clinical operations, statistical programming, and biometrics teams.
The partner company focuses on clinical research and data management to advance healthcare. They offer a collaborative remote environment with a focus on operational excellence.
Lead the development, testing, and support of clinical databases from startup through post-lock.
Partner with Data Management, Project Management, EDC vendors, and clients to guide database design and programming.
Mentor junior programmers, train end users, and shape the new regional team's growth and processes.
Precision Medicine Group is a specialized life sciences company that accelerates the development and commercialization of precision medicines. The company is expanding across LATAM and values collaboration, technical leadership, and innovation.
Coordinate day-to-day clinical trial operations remotely, ensuring compliance with protocols and regulations.
Support remote patient visits including scheduling, documentation, and follow-up.
Maintain accurate data entry in EDC/CTMS systems and assist with regulatory documentation.
UniTriTeam is a global leader in providing operational, administrative, and technology support to clinical research sites. They have a mission-driven, supportive, and inclusive team culture.
Build and administer EDC trials using Veeva CDMS for client projects.
Perform eCRF design, edit check programming, and test data creation.
Manage interface connections and ensure high-integrity database imports.
Celerion is an agile clinical research organization that uses translational medicine to accelerate drug development. The company values integrity, trust, teamwork, and respect and seeks performance-oriented, innovative team players.
Provide operational leadership and oversight of clinical data management activities across studies, ensuring high-quality, inspection-ready data.
Manage end-to-end data management from study start-up through database lock, with oversight of CROs, vendors, and internal stakeholders.
Drive data quality, compliance, and continuous improvement, serving as primary Data Management representative on cross-functional teams.
Definium Therapeutics is a late-stage clinical biopharmaceutical company applying scientific rigor to psychedelics to develop accessible treatments for psychiatric disorders. It is headquartered in New York and publicly traded on Nasdaq under the symbol DFTX.
Oversee day-to-day management of third-party vendors throughout clinical study lifecycle.
Develop and implement vendor oversight plans and monitor performance through KPIs and governance meetings.
Facilitate cross-functional collaboration to resolve issues and ensure compliance with GCP and regulatory requirements.
The company is a clinical research organization that manages clinical trials and third-party vendors. The team size is not specified, but the culture is collaborative and quality-focused.
Lead data management projects with full responsibility for planning, execution, monitoring, and closure.
Serve as primary point of contact for internal teams and external vendors.
Ensure compliance with data standards and manage project risks.
Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We have a collaborative, international team where people share ideas and grow their careers.
Manage the intake, review, analysis, and reporting of Individual Case Safety Reports (ICSRs) and support Clinical Events Committees and Data Monitoring Committees.
Co-author and maintain study-specific safety documents and prepare aggregate safety reports for regulatory submission.
Collaborate with sponsors, study teams, and cross-functional partners to ensure data quality and compliance with GCP and GVP standards.
This partner company delivers high-quality safety services across clinical research and medical device programs. They foster a collaborative, detail-oriented environment with a focus on compliance and patient outcomes.
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.