Clinical Research Associate Manager – Neurology

🔥 14 hours ago

🏖️ New Jersey – Remote

🏖️ New Jersey – Remote

💵 $142.4k - $224.1k / year

⏰ Full Time

🟡 Mid-level

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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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

• Manage a team of 6–14 Clinical Research Associates • Ensure study and site performance adheres to local regulations, company SOPs, and ICH GCP • Provide training, support, mentoring, career development, and performance reviews for CRAs • Manage low-performance situations and resolve escalated issues • Allocate work and support efficient resource utilization • Contribute to capacity planning, manpower reporting, and CRA forecasting • Coordinate with CRAs, Partner Line Managers, Clinical Research Managers, and other functions on processes and protocol implementation • Interact with sites to resolve operational issues • Attend local Investigator Meetings when requested • Interface with Global Clinical Trial Organization partners on clinical trial execution • Escalate site performance issues to the Clinical Research Manager and Clinical Research Director • Liaise with local HR and finance functions • Ensure CRA compliance with corporate policies, procedures, and quality standards • Travel up to 50%

🎯 Requirements

• Bachelor’s degree in Science • Minimum of 5 years’ experience within Clinical Research • Minimum of 3 years’ experience as a CRA monitoring clinical trials • Line management experience preferred, or at minimum team leader experience • Fluent in the local language • Business proficient in English, verbal and written • Excellent working knowledge of applicable ICH/GCP regulations and Good Documentation Practices • Expertise in core trial management systems and tools • Ability to work independently and in a team environment • Excellent people management, time management, project management, and organizational skills • Strong leadership, interpersonal, communication, and conflict management skills • Demonstrated ability to build relationships and communicate effectively with external customers, sites, and investigators • Up to 50% travel • Must be a US or Puerto Rico resident • No visa sponsorship available

🏖️ Benefits

• Annual bonus • Long-term incentive, if applicable • Medical, dental, and vision healthcare • Other insurance benefits for employee and family • Retirement benefits, including 401(k) • Paid holidays • Vacation • Compassionate and sick days • Remote work arrangement • No relocation