
Clinical Research Associate Manager – Neurology
Posted 1 day ago

Posted 1 day ago
This is a fully remote position, open to applicants in New Jersey.
• Oversee a team consisting of 6–14 Clinical Research Associates.
• Ensure that study and site performance complies with local regulations, company standard operating procedures (SOPs), and ICH Good Clinical Practice (GCP).
• Provide training, guidance, mentoring, career development opportunities, and conduct performance evaluations for CRAs.
• Address low-performance situations and manage escalated issues effectively.
• Allocate tasks and promote efficient resource utilization.
• Assist in capacity planning, manpower reporting, and CRA forecasting.
• Collaborate with CRAs, Partner Line Managers, Clinical Research Managers, and other departments regarding processes and protocol implementation.
• Engage with sites to troubleshoot operational challenges.
• Attend local Investigator Meetings as required.
• Collaborate with Global Clinical Trial Organization partners on the execution of clinical trials.
• Report site performance concerns to the Clinical Research Manager and Clinical Research Director.
• Coordinate with local HR and finance departments.
• Ensure CRA adherence to corporate policies, procedures, and quality standards.
• Willingness to travel up to 50% of the time.
• Bachelor’s degree in a Science-related field.
• At least 5 years of experience in Clinical Research.
• Minimum of 3 years' experience as a CRA monitoring clinical trials.
• Preferably have line management experience or, at the very least, experience as a team leader.
• Proficiency in the local language.
• Business-level proficiency in English, both verbal and written.
• Strong working knowledge of relevant ICH/GCP regulations and Good Documentation Practices.
• Familiarity with core trial management systems and tools.
• Ability to work independently as well as collaboratively in a team setting.
• Exceptional skills in people management, time management, project management, and organization.
• Strong leadership, interpersonal, communication, and conflict resolution abilities.
• Proven capability to establish relationships and communicate effectively with external customers, sites, and investigators.
• Willingness to travel up to 50%.
• Must be a resident of the US or Puerto Rico.
• Visa sponsorship is not available.
• Annual bonus.
• Long-term incentives, if applicable.
• Comprehensive medical, dental, and vision healthcare coverage.
• Additional insurance benefits for employees and their families.
• Retirement benefits, including a 401(k) plan.
• Paid holidays.
• Vacation time.
• Compassionate and sick leave days.
• Opportunities for remote work arrangements.
• No relocation assistance provided.
ICON plc
EDETEK Inc.
ICON plc
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