Everest Clinical Research

Statistical Programmer I

Master’s or Ph.D. in statistics/biostatistics/epidemiology/public health/bioinformatics/mathematics/computer sciences; at least 1 year of clinical trial programming experience.

Clinical Trial IWRS Monitor

Bachelor's degree in health science or related field with at least 3 years in clinical trial data processing and management.

Clinical Trials IWRS Monitor

Bachelor's degree in health sciences with 3+ years in clinical trial data processing and management; independent work ability, professional communication, and meticulous data review.

Clinical Trial IWRS Monitor (Overnight)

Bachelor's degree in health science or related field with at least 3 years' experience in clinical trial data processing and management; ability to work independently and communicate effectively.

Senior Clinical Trial IWRS Monitor

Bachelor's in health science/CS; 5+ years clinical trial data processing; experience in clinical research and call center support; strong communication; 4+ years in SDLC, project management.

Clinical Trial IWRS Monitor I

Bachelor's degree in health science or related field with at least 3 years' experience in clinical trial data processing and management; ability to work independently and communicate clearly.

Medical Writer

Advanced degree; 2+ years medical writing in pharma; regulatory submission experience preferred; remote or on-site in Canada; strong writing, QC, and project coordination.

Clinical Safety Data Associate

RN/MD/MSc/PhD or equivalent; 2-3 years in clinical trial data management; medical coding knowledge; strong communication and organization; ability to manage multiple projects.

Clinical Research Safety Associate

MSc or PhD in clinical/medical/health field; 2+ years clinical research experience; Phases I-IV exposure; strong communication; MS Office; ability to work in team/independently.

Senior Statistical Programmer

Master’s or Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science with 4+ years in clinical trial programming, or Bachelor’s with 6+ years.

Clinical Data Manager

Bachelor's in health/pharma/chemistry with 2+ years clinical data management; strong leadership and regulatory knowledge.

Senior Clinical Trial Analytics Monitor I

Senior Clinical Trial Analytics Monitor

Bachelor’s in health science, computer science, or related field; 5+ years in clinical data analytics/BI; 4+ years in SQL, PL/SQL, R, Python or SAS; experience with clinical data standards; strong client interaction and project delivery skills.

Senior Medical Writer

Experience in medical writing for regulatory submissions; advanced degree preferred; 5+ years in pharmaceutical clinical trials; strong editing, project management, and ICH/GCP knowledge.

Senior Clinical Data Manager

5+ years pharma clinical data management or 2+ years as CDM II; Bachelor's or Master's in health/pharma/sciences; strong CDM knowledge and leadership.

Bachelor's in health/pharma sciences with 2+ years in clinical data management; leads data projects; strong understanding of clinical data management concepts and regulations.

Statistical Programmer II

Master’s or Ph.D. in statistics/biostatistics/epidemiology/public health/bioinformatics/mathematics/computer science with at least two years’ experience in clinical trial statistical programming and data analysis.

Master’s in Math/Statistics with at least five years of experience in statistical programming.

Clinical Data Management Specialist

Bachelor's or Master's in health/pharma sciences, physical/biological, or chemistry; ability to work independently; data management and clinical trial data capture knowledge.

Clinical Trial Web Application Developer

Web Application Developer

BS in CS; 8+ years’ experience; full-stack web app development; Java/J2EE security; SDLC/Agile; Unix/Windows

Design, develop, test, deploy, and maintain Java web applications; full-stack development; collaborate with clients and cross-functional teams; ensure quality and security.

Bachelor's degree; 5+ years in clinical trial data processing/management; experience in clinical research and call center support; strong client communication; knowledge of CLT processes and software lifecycle.

Bachelor's degree in health science or related field; at least 3 years’ experience in clinical trial data processing/management; ability to work independently and communicate professionally.

Title	Location	Date
Statistical Programmer I Full Time · 1+ YOE Manila, Philippines, Philippines · Remote	Manila, Philippines, Philippines Remote	Jan 21, 2026
Clinical Trial IWRS Monitor Full Time · 3+ YOE Taipei City, Taiwan, Taiwan · Remote	Taipei City, Taiwan, Taiwan Remote	Jan 20, 2026
Clinical Trial IWRS Monitor Full Time · 3+ YOE Sofia, :, Bulgaria · Remote	Sofia, :, Bulgaria Remote	Jan 20, 2026
Clinical Trial IWRS Monitor (Overnight) Full Time · $45K-$65K · 3+ YOE Markham or Canada · Hybrid	Markham or Canada Hybrid	Jan 16, 2026
Senior Clinical Trial IWRS Monitor Full Time · $70K-$90K · 5+ YOE Markham or Canada · Hybrid	Markham or Canada Hybrid	Jan 13, 2026
Clinical Trial IWRS Monitor I Full Time · $45K-$65K · 3+ YOE Markham or Remote · Hybrid	Markham or Remote Hybrid	Jan 13, 2026
Medical Writer Full Time · $65K-$100K · 2+ YOE Remote or Markham · Hybrid	Remote or Markham Hybrid	Jan 13, 2026
Clinical Safety Data Associate Full Time · $60K-$80K · 2+ YOE Markham or Canada · Hybrid	Markham or Canada Hybrid	Jan 13, 2026
Clinical Research Safety Associate Full Time · $60K-$85K · 2+ YOE Markham or Remote · Hybrid	Markham or Remote Hybrid	Jan 13, 2026
Senior Statistical Programmer Full Time · 4+ YOE Warsaw, Masovian Voivodeship, Poland · Remote	Warsaw, Masovian Voivodeship, Poland Remote	Jan 12, 2026
Clinical Data Manager Full Time · $60K-$90K · 2+ YOE Markham or Remote · Hybrid	Markham or Remote Hybrid	Jan 9, 2026
Senior Clinical Trial Analytics Monitor I Full Time · $100K-$120K · 5+ YOE Markham or Canada · Remote	Markham or Canada Remote	Jan 9, 2026
Senior Medical Writer Full Time · $90K-$140K · 5+ YOE Markham or Canada · Hybrid	Markham or Canada Hybrid	Jan 6, 2026
Senior Clinical Data Manager Full Time · 5+ YOE Warsaw, Masovian Voivodeship, Poland · Remote	Warsaw, Masovian Voivodeship, Poland Remote	Jan 2, 2026
Clinical Data Manager Full Time · 2+ YOE Warsaw, Mazowieckie, Poland · Remote	Warsaw, Mazowieckie, Poland Remote	Jan 2, 2026
Statistical Programmer II Full Time · 2+ YOE Warsaw, Mazowieckie, Poland · Remote	Warsaw, Mazowieckie, Poland Remote	Oct 3, 2025
Senior Statistical Programmer Full Time · 5+ YOE United Kingdom · Remote	United Kingdom Remote	Jun 16, 2025
Clinical Data Management Specialist Full Time · $45K-$70K Markham or Remote · Hybrid	Markham or Remote Hybrid	Jan 14, 2025
Clinical Trial Web Application Developer Full Time · 8+ YOE Bucharest or Bucharest · Hybrid	Bucharest or Bucharest Hybrid	Jan 14, 2025
Clinical Trial Web Application Developer Full Time · $90K-$125K · 8+ YOE Markham or Canada · Hybrid	Markham or Canada Hybrid	Jan 14, 2025
Senior Clinical Trial IWRS Monitor Full Time · 5+ YOE Sofia, Sofia City, Bulgaria · Hybrid	Sofia, Sofia City, Bulgaria Hybrid	Jan 14, 2025
Clinical Trial IWRS Monitor Full Time · 3+ YOE Sofia, ., Bulgaria · Remote	Sofia, ., Bulgaria Remote	Jan 14, 2025

Name	Everest Clinical Research
Headquarters	CA
Industries	BiotechnologyPharmaceuticals
Activities	Clinical trials managementBiostatistical analysisClinical data managementRegulatory submission supportMedical writing
Type	Private
Employees	700
Parent Company	Arlington Capital Partners
Tagline	Full-service contract research organization for clinical drug development.
Founded	2,004
Website	everestclinical.com
Latest Funding Round	Private Equity
Latest Funding Year	2,020
Latest Investors	Arlington Capital Partners

Everest Clinical Research

About Everest Clinical Research