MSD is a leading biopharmaceutical company known as Merck & Co. , Inc. in the United States, Canada, and Puerto Rico, and as MSD globally. The company focuses on scientific innovation to deliver medicines and vaccines for various health challenges, including oncology, vaccines, infectious diseases, and cardio-metabolic diseases. MSD operates multiple divisions, including Human Health, Animal Health, and Research & Development. With approximately 75,000 employees worldwide and a significant investment in research and development, MSD is committed to improving global health through its scientific advancements. Additionally, the company places a strong emphasis on diversity, inclusion, and corporate responsibility. MSD’s operations extend worldwide, offering opportunities in numerous regions and promoting diversity and innovation in all aspects of its business.
4 days ago
🌾 Iowa – Remote
🌪️ Kansas – Remote
+3 more states
💵 $139.6k - $219.7k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor
MSD is a leading biopharmaceutical company known as Merck & Co. , Inc. in the United States, Canada, and Puerto Rico, and as MSD globally. The company focuses on scientific innovation to deliver medicines and vaccines for various health challenges, including oncology, vaccines, infectious diseases, and cardio-metabolic diseases. MSD operates multiple divisions, including Human Health, Animal Health, and Research & Development. With approximately 75,000 employees worldwide and a significant investment in research and development, MSD is committed to improving global health through its scientific advancements. Additionally, the company places a strong emphasis on diversity, inclusion, and corporate responsibility. MSD’s operations extend worldwide, offering opportunities in numerous regions and promoting diversity and innovation in all aspects of its business.
• This role will be key to ensure strong monitoring in our clinical trials. • Responsible to manage a team of 6-14 CRAs. • Ensure excellent study and site performance with adherence to local regulations. • Support and resolve escalation of issues from CRAs. • Manage local conflicts between resource and work. • Provides training, support and mentoring to the CRA.
• Minimum of 5 years´ experience within Clinical Research • Minimum of 3 years’ experience as CRA monitoring clinical trials • Line management experience preferred or at the minimum team leader experience • Bachelor’s degree in science
• bonus eligibility • long term incentive if applicable • health care and other insurance benefits (for employee and family) • retirement benefits • paid holidays • vacation • sick days
Apply Now4 days ago
Perform study monitoring visits for clinical research at Agilent, focusing on quality and compliance.
🇺🇸 United States – Remote
💵 $79.2k - $148.5k / year
💰 Post-IPO Debt on 2019-09
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor
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