Explore 25 Jobs at Everest New Logo
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Posted 10 days ago
The Clinical Data Management Specialist supports clinical trial data activities for assigned studies, including data entry, database and Case Report Form design, data validation, quality control, and documentation. The role also assists with data management plans, monitoring reports, coding discrepancy resolution, and preparation of trial records for archiving.
Key Details
Top Skills Required
Top Benefits
Posted 10 days ago
The Senior Medical Writer authors, edits, reviews, and finalizes clinical and regulatory documents for clinical trials and regulatory submissions. The role leads writing projects, manages sponsor relationships and review cycles, monitors quality and timelines, and contributes to medical-writing standards and professional development.
Key Details
- full time Jobs
- $90,000 - $140,000 per year
- 5+ years experience
Top Skills Required
Top Benefits
Posted 10 days ago
The Senior Clinical Trial Analytics Monitor I supports clinical trial analytics and reporting, including standardizing dashboards, reports, metrics, and KPIs across business units. The role also manages CTT CDD startup and development activities, including requirements, testing, user support, demonstrations, quality assurance, and capability development.
Key Details
- full time Jobs
- $100,000 - $120,000 per year
- 5+ years experience
Top Skills Required
Top Benefits
Posted 10 days ago
The Senior Clinical Database Designer develops and maintains clinical trial database capabilities, including designing CRFs and EDC systems, authoring validation specifications, and coordinating database testing. The role also supports clinical data management activities, data quality and query resolution, regulatory and procedural compliance, and develops SAS code for logical checks and monitoring reports.
Key Details
- full time Jobs
- $100,000 - $140,000 per year
- 5+ years experience
Top Skills Required
Top Benefits
Posted 10 days ago
The Manager, Clinical Data Management leads clinical trial data management programs and teams, overseeing client relationships, project plans, deliverables, budgets, resources, and staff development. The role also contributes to improving data management systems and standards, business development, and recruitment; it requires a relevant bachelor's degree or higher and 11 years of related experience.
Key Details
- full time Jobs
- $140,000 - $170,000 per year
- 11+ years experience
Top Skills Required
Top Benefits
Posted 10 days ago
The Medical Writer prepares, edits, quality-checks, and publishes clinical and regulatory documents, including clinical study reports, protocols, scientific publications, and supporting materials. The role also supports project timelines, literature searches, TLG assembly, and potential Data Monitoring Committee administration while working with project teams and sponsors.
Key Details
- full time Jobs
- $65,000 - $100,000 per year
- 2+ years experience
Top Skills Required
Top Benefits
Posted 10 days ago
The Clinical Database Designer designs and maintains clinical study databases in electronic data capture systems, including forms, edit checks, roles, integrations, and testing. The role also reviews study specifications, supports data management and quality assurance, maintains design standards, and contributes to project planning and database-design tools.
Key Details
- full time Jobs
- $50,000 - $100,000 per year
- 1+ years experience
Top Skills Required
Top Benefits
Posted 12 days ago
The Clinical Trial Assistant supports clinical trial operations by coordinating study documentation, regulatory submissions, Trial Master Files, site activities, vendors, and trial supplies. The role also assists with monitoring compliance, safety report distribution, data reporting, invoicing, training, and audit or inspection readiness.
Key Details
Top Skills Required
Top Benefits
Posted 17 days ago
The PK Scientist II conducts pharmacokinetic/pharmacodynamic analysis, modeling, and predictive simulations to support clinical trial design, drug development, and regulatory submissions. Responsibilities include authoring and reviewing PK/PD plans, protocols, reports, and related clinical pharmacology documents, while maintaining compliance with applicable standards and guidelines.
Key Details
- full time Jobs
- $105,000 - $120,000 per year
- 2+ years experience
Top Skills Required
Top Benefits
Posted 17 days ago
The Clinical Trial Web Application Developer designs, develops, tests, deploys, and maintains custom Java web applications for clinical research clients. Responsibilities include full-stack implementation, database and security work, requirements analysis, technical documentation, client support, and ongoing application improvements.
Key Details
- full time Jobs
- $90,000 - $125,000 per year
- 8+ years experience
Top Skills Required
Top Benefits
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