Clinical Research Associate Manager - Neurology

• Work allocation, staff development and performance appraisal. • Provides input for capacity planning, including reporting of current manpower and forecasting of CRA capacity and needs, to provide efficient use of resources. • Work with CRAs, PLMS and other functions to ensure consistency of processes and protocol implementation across the country, to reduce variability and provide predictability. • Interacts with sites as needed to resolve site or CRA operational issues to meet commitments in a timely manner in coordination with the study CRM. • Attend local Investigator Meetings if requested to. • Interface with Global Clinical Trial Organization (GCTO) partners on clinical trial execution. • Escalates site performance issues to CRM and Clinical Research Director (CRD).

Job Description This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director or Head of Site Management and Monitoring, the person is responsible to manage a team of 6-14 Clinical Research Associates (CRAs) and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP. As line manager the role is critical to continuously develop key talents by providing training, support and mentoring to the CRAs and properly manage situation of low or non-performance. The role will work at country level with other local stakeholder e.g. Clinical Research Managers (CRMS) to ensure alignment and development of the country capabilities. The role will collaborate with country Partner Line Managers (PLMS) to ensure alignment across all monitoring functions. The person contributes to HQ capacity/resource planning activities to ensure efficient allocation of resources and work. Responsibilities include, but are not limited to: • Work allocation, staff development and performance appraisal. • Provides input for capacity planning, including reporting of current manpower and forecasting of CRA capacity and needs, to provide efficient use of resources. • Work with CRAs, PLMS and other functions to ensure consistency of processes and protocol implementation across the country, to reduce variability and provide predictability. • Interacts with sites as needed to resolve site or CRA operational issues to meet commitments in a timely manner in coordination with the study CRM. • Attend local Investigator Meetings if requested to. • Interface with Global Clinical Trial Organization (GCTO) partners on clinical trial execution. • Escalates site performance issues to CRM and Clinical Research Director (CRD). People and Resource Management: • Manage CRA – career development, performance reviews, etc., including addressing low-performance situations, and taking appropriate actions. • Support and resolve escalation of issues from CRAs. • Liaise with local HR and finance functions as required. • Contribute to HQ capacity/resource planning activities to ensure efficient allocation of resources and work. Manage local conflicts between resource and work. • Provides training, support and mentoring to the CRA to ensure continuous development. • Ensures CRA compliance to corporate policies, procedures and quality standards Extent of Travel: up to 50% Qualifications, Skills & Experience CORE Competency Expectations: • Ability to work independently and in a team environment. • Excellent people management, time management, project management and organizational skills. • History of strong performance. • Skills and judgment required to be a good steward/decision maker for the company. • 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 and ability to work within these guidelines. • Expertise in and excellent working knowledge of core trial management systems and tools. Behavioral Competency Expectations: • High emotional intelligence. • Strong leadership skills with proven success in people management. • Excellent interpersonal and communication skills, conflict management. • Demonstrated ability to build relationships and to communicate effectively with external customers (e.g. sites and investigators). • Influencing skills. Experience Requirements: Required: • 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. Educational Requirements: Required: • Bachelor’s degree in Science. Preferred: • Advanced degree, (e.g. BA/BS or higher) with a strong emphasis in science and/or biology. #eligibleforERP #clinicaltrialjobs Required Skills: Adaptability, Adaptability, Clinical Research, Clinical Research Methods, Clinical Study Management, Clinical Study Protocols, Clinical Trials Marketing, Conflict Management, Continuous Development, Data Reporting, Emotional Intelligence, Ethical Standards, Global Coordination, ICH GCP Guidelines, Leadership Management, Leadership Theories, Liaison Work, Line Management, Logical Thinking, Multiple Therapeutic Areas, Organizational Leadership, People Leadership, People Management, Performance Monitoring, Procedure Adherence {+ 9 more} Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement​ We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your r