Clinical Research Associate Manager

🔥 1 hour ago

🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

💵 $142.4k - $224.1k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

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MSD

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1891

🏥 Healthcare

📦 Logistics

🧬 Biotechnology

Healthcare • Logistics • Biotechnology

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.

📋 Description

• Ensure strong monitoring in our clinical trials • Manage a team of 6-14 CRAs • Ensure excellent study and site performance with adherence to local regulations, company SOPs, and ICH GCP • Provide training, support, and mentoring to the CRAs • Manage situation of low or non-performance • Work allocation, staff development, and performance appraisal • Provide input for capacity planning • Ensure consistency of processes and protocol implementation across the country • Interact with sites to resolve operational issues • Manage CRA career development and performance reviews • Ensure CRA compliance to corporate policies, procedures, and quality standards

🎯 Requirements

• 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 • Fluent in Local Language and business proficient in English (verbal and written) • Excellent working knowledge of all applicable ICH/GCP regulations and Good Documentation Practices • Expertise in and excellent working knowledge of core trial management systems and tools

🏖️ Benefits

• medical • dental • vision healthcare and other insurance benefits (for employee and family) • retirement benefits, including 401(k) • paid holidays • vacation • compassionate and sick days