Participate in CRF design, database review, and data validation procedures to ensure data integrity.
Produce data listings, summary tables, and graphics for interim and final analyses of clinical trials.
Collaborate with Biometrics functions and coordinate data transfer standards with CROs and vendors.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, they maintain a supportive culture focused on quality, professional development, and low turnover.
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.
Design, develop, and validate CDISC-compliant SDTM and ADaM datasets for clinical trials.
Support regulatory submissions including ISS, ISE, and create Tables, Listings, and Figures.
Collaborate with cross-functional teams to deliver accurate statistical outputs for evidence-based healthcare.
The partner company is a clinical research organization that supports impactful clinical programs through statistical programming. It offers a collaborative culture and a flexible remote work environment.
Develop, validate, and maintain SAS and/or R programs for SDTM, ADaM datasets, and TLFs per CDISC standards.
Support statistical analyses for regulatory submissions, safety reports, and clinical study reports in a GxP-compliant environment.
Collaborate with cross-functional teams to define analysis specifications and perform quality control on statistical outputs.
Iovance Biotherapeutics is a global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) therapy for cancer. The company is a fast-paced biotech with a collaborative culture, committed to continuous innovation in cell therapy.
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.
Provide high-level consulting services for statistical analysis, reporting, and programming in clinical trials.
Develop and validate statistical analysis plans, randomization schedules, and clinical trial reports.
Mentor statistical programmers and ensure compliance with regulatory guidelines like ICH, GCP, and 21 CFR Part 11.
eClinical Solutions helps life sciences organizations accelerate clinical development initiatives with expert data services and the elluminate Clinical Data Cloud. It is a fast-growing company that has won the 2025 Top Workplaces USA Award for Remote Work and emphasizes an inclusive culture and work-life balance.
Lead the development and execution of statistical analysis plans for large-scale real-world evidence studies.
Work directly with cross-functional teams and senior stakeholders to design data-driven solutions for a high-profile sponsor.
Oversee and mentor junior analysts, driving best practices and innovative analytics workflows.
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals in more than 20 countries, the company emphasizes a supportive culture, continuous training, and below-industry-average turnover rates.
Leads a global team of Statistical Programmers, overseeing SDTM, ADaM, and TLF deliverables.
Ensures quality, budget, and timeline adherence while mentoring team members.
Contributes to process improvements and strategic initiatives to enhance operational efficiency.
Ergomed is a specialist clinical research organization focused on rare disease and oncology clinical trials. They have built a collaborative, international team across multiple continents, valuing teamwork, flexibility, and work-life balance.
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.
Leads the planning, conduct, and oversight of clinical studies per scope of work, ensuring compliance with protocols, SOPs, and regulatory requirements.
Acts as primary clinical point of contact for clients, develops study documents, and drives site feasibility and recruitment strategies.
Manages clinical teams, training, vendor oversight, and ensures data quality and timely deliverables across study phases.
Precision Medicine Group is a clinical research organization that provides outsourced clinical trial management services to pharmaceutical and biotechnology companies. The company fosters a collaborative culture focused on quality and compliance, and employs a team of experienced clinical professionals.
Manage clinical elements of trials including site selection, start-up, enrollment, monitoring, and close-out for studies across multiple countries.
Lead CRAs and ensure timeline adherence, quality delivery, and effective communication with cross-functional teams and sponsors.
Identify risks to project timelines, create action plans, and mentor team members while maintaining focus on study priorities.
Precision for Medicine is a precision medicine CRO that combines novel clinical trial designs, biomarker and data analytics, with a focus on rare diseases and oncology. The company is part of Precision Medicine Group, a growing organization dedicated to advancing oncology development and positively impacting patient health.
Lead data management activities for clinical and epidemiologic research studies from start-up through closeout.
Perform advanced SAS programming to clean, validate, and manage complex research datasets.
Design and maintain study databases, validation rules, and data quality procedures.
DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering, and digital transformation. The company employs experts in public health and health operations and is committed to innovation and improving lives.
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.
Independently perform statistical analyses for clinical studies and research initiatives.
Develop statistical analysis plans, including sample size and power calculations.
Collaborate with cross-functional teams to ensure statistical rigor and appropriate interpretation of results.
Karius is a life science, venture-backed clinical metagenomics company focused on elevating patient care through microbial insights. The company delivers unprecedented diagnostic insight detecting microbial cell-free DNA to assist physicians in making rapid treatment decisions.
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.
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.
Provide leadership and mentorship across regional clinical trials while ensuring high-quality study execution with minimal travel.
Oversee monitoring visit reports, manage study risks, and ensure compliance with corrective measures at country and regional levels.
Collaborate with cross-functional teams, lead project calls, and deliver training to support data integrity and site performance.
PSI CRO is a privately owned, global Contract Research Organization dedicated to advancing medical science and bringing new therapies to patients worldwide. Founded in 1995, the company has over 3,000 employees and prides itself on long-term stability, having never undergone a merger, acquisition, or company-wide layoffs.
Serve as the primary point of contact for customers, forming trusted relationships and owning complex technical implementation projects from kickoff through go-live.
Consult with customer technical teams on data extraction, transformation, and loading from EMR, ADC, and other systems into the Bluesight platform.
Validate, reconcile, and analyze data using command-line tools and scripts, produce technical procedures, and collaborate cross-functionally to improve processes.
Bluesight creates groundbreaking solutions that increase efficiency, safety, and visibility for health systems, hospital pharmacy, and pharmaceutical manufacturers. It is a high growth healthcare information technology company with a start-up vibe and over 3,000 customers using proven solutions.