
1001 - 5000 employees
Founded 1997
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
🔥 10 minutes ago
🍂 Massachusetts – Remote
đź’µ $140.3k - $153.5k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
đź‘» Ghost score 8%
Where this job comes from
Posted on ERGOMED's careers page, not through a job board
First seen by Remote Rocketship 10 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
Founded 1997
đź’Ľ Consulting
🏥 Healthcare
📦 Logistics
Consulting • Healthcare • Logistics
ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.
• Perform on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visits • Ensure investigational facilities and staff remain adequate throughout the study • Identify investigators and verify their qualifications, resources, facilities, equipment, and staff • Train investigational site staff as necessary • Support preparation of regulatory and/or EC submissions when applicable • Mentor and train new staff • Perform co-monitoring visits to assess junior staff performance
• College/University degree in Life Sciences or an equivalent combination of education, training & experience • Extensive on-site monitoring experience in phase 2/3 trials • Ideally, experience with complex trials in oncology or rare disease • Full working proficiency in English • Ability to plan, multitask and work in a dynamic team environment • Communication, collaboration, and problem-solving skills • Ability to travel nationally
• Remote work options • Collaborative and passionate team environment • Opportunities to make a real difference to patients' lives • Diverse and inclusive workplace where every voice counts
Apply Now🔥 8 hours ago
Senior Clinical Research Associate monitoring sponsor-dedicated clinical trials at ICON. Coordinating study setup, monitoring, documentation, compliance, and stakeholder relationships.
🇺🇸 United States – Remote
đź’µ $110.5k - $138.2k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🔥 13 hours ago
Senior Clinical Research Associate monitoring dermatology and rheumatology clinical trials for Indero, a contract research organization. Conducting site visits, compliance checks, source data verification, and regulatory documentation.
🔥 14 hours ago
Senior CRA overseeing oncology clinical trials for Worldwide Clinical Trials, a global contract research organization. Managing site monitoring, regulatory compliance, data quality, and study delivery across the US West Coast.
🇺🇸 United States – Remote
đź’µ $97k - $193k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor
🔥 14 hours ago
Senior CRA monitoring CNS clinical trials for Worldwide Clinical Trials, a global CRO. Managing Midwest investigative sites, regulatory compliance, data quality, and site visits.
🇺🇸 United States – Remote
đź’µ $97k - $193k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor
🔥 14 hours ago
Clinical data management study lead overseeing Regeneron pharmaceutical trial data, quality, databases, and CRO deliverables. Managing complex studies from planning through database lock and close-out.
🇺🇸 United States – Remote
đź’µ $114.8k - $187.4k / year
đź’° Post-IPO Equity on 2023-10
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor