Lead and oversee clinical data management activities across assigned studies, ensuring high-quality data in compliance with ICH-GCP and company SOPs.
Manage CROs and external vendors, including database start-up, data cleaning, and database lock, while maintaining quality, timelines, and budget.
Collaborate cross-functionally with Biometrics, Clinical Operations, Medical, and other teams to drive data management milestones and inspection readiness.
Clinical Data ManagementEDC SystemsGCP/ICH GuidelinesCDISC StandardsCRO Management
Lead clinical data management strategy and execution across the portfolio to ensure data integrity and regulatory submission readiness.
Own end-to-end database lock planning and execution for pivotal trials, ensuring on-time, audit-ready locks.
Build and lead a fit-for-purpose data management team, including internal staff and outsourced functions, and establish SOPs and governance.
Prilenia is a private biopharmaceutical company focused on bringing transformative medicines to people with neurodegenerative diseases such as ALS and Huntington’s disease. They are a small to mid-size clinical-stage organization with a highly committed global team and a flexible, mostly remote culture.
Manage all aspects of clinical trial data management from study start-up to post-database lock for assigned projects.
Oversee database development, edit check specifications, data entry quality, and data management documentation.
Act as the lead data management contact, coordinating with sponsors, vendors, and cross-functional teams.
Precision Medicine Group is a global provider of clinical development, data management, and related services for the biopharmaceutical industry. The company maintains a collaborative, quality-driven culture and values diversity and inclusion across its global teams.
Assist in preparing clean databases by reviewing clinical trial data through CDMS or external data listings to ensure compliance with protocols.
Generate queries to resolve data discrepancies and support the development of CRFs and edit check specifications.
Maintain documentation related to CRF and data listing testing, including user acceptance testing.
Premier Research is a global clinical research, product development, and consulting company that helps biotech and specialty pharma transform life-changing ideas into new medical treatments. The company values teamwork, agility, and care for patients, providing a diverse culture with opportunities for growth and continuous learning.
Process external and local lab data throughout the clinical trial lifecycle using the elluminate platform.
Perform QC of laboratory normal ranges, test transfers, and data listings to ensure ICH/GCP and 21 CFR Part 11 compliance.
Collaborate with clinical data management and cross-functional teams to support study start-up, external vendor data transfers, and data quality.
eClinical Solutions helps life sciences organizations accelerate clinical development with expert data services and the elluminate Clinical Data Cloud. The company is a people-first, inclusive organization and a 2025 Top Workplaces USA Award winner for Remote Work.
Manage all clinical aspects of assigned studies across multiple countries, ensuring timeline adherence and quality.
Lead CRAs and support site selection, start-up, enrolment, monitoring, data cleaning, and close-out.
Identify risks to timelines and collaborate with teams to deliver high client satisfaction.
Precision for Medicine is a precision medicine CRO combining novel trial designs, operational experts, and biomarker analytics with a focus on oncology and rare diseases. It encourages high-energy professionals who thrive in dynamic environments.
Defines enterprise technical governance and strategy for clinical data management across Latin America.
Oversees database design, testing, integration, and archival to ensure compliance and quality.
Mentors technical teams and drives innovation in data platforms and processes.
Precision Medicine Group is a life sciences company specializing in precision medicine solutions. They are expanding their data management capabilities across Latin America, building a new regional technical data management organization.
Oversee GCP compliance, manage deviations and CAPAs, and conduct quality and TMF reviews.
Maintain inspection readiness and support CRO oversight per ICH E6(R3).
Collaborate with Data and Clinical teams to embed compliance into workflows and train teams.
Resilience Care is a French medtech founded in 2021, offering AI remote monitoring for oncology, gastroenterology, and psychiatry. It serves 35,000 patients across 200+ facilities with an agile, collaborative culture.
Lead and oversee global Phase 0-4 clinical trials with cross-functional teams from inception to closure.
Manage external vendors, recruitment strategies, and study systems to ensure quality, efficiency, and inspection readiness.
Collaborate with study project managers to drive timelines, budgets, and compliance with ICH/GCP and AbbVie policies.
AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and Allergan Aesthetics. They are a global, science-driven pharmaceutical company committed to integrity, innovation, and serving the community.
Lead and coach a team of Clinical Study Operations professionals overseeing device-based clinical trials from feasibility to close-out.
Drive domain-level ClinOps initiatives including process standardization, tooling, and data quality improvements.
Represent ClinOps in business development conversations, feasibility discussions, and Investigator Meetings, ensuring operational readiness.
Beacon Biosignals transforms precision medicine for the brain, offering at-home EEG and diagnostic platforms for neurological, psychiatric, and sleep disorders. They are a remote-first, distributed company with hubs in Boston, New York, and Paris, emphasizing curiosity, sound judgment, and empathy.