Associate Director - Clinical Data Manager

This role can be done in a fully remote working model.
Your role:
A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team. As an Associate Director Clinical Data Manager, you will play a crucial role in managing and overseeing clinical data management activities within the organization. You will be responsible for ensuring the integrity, accuracy, and completeness of clinical trial data, while also coordinating a team of clinical data management professionals in a matrix setting. You will be accountable for all Clinical Data Management (CDM) related deliverables in assigned global (Phase I-IIIb) trials or programs of varying complexity. Provide CDM leadership for assigned trial(s)/program(s), take global accountability and serve as the CDM representative at the study/program level. Demonstrate project management and operational expertise in the strategic planning and delivery of CDM deliverables at study/program level, e.g. planning timelines and resources, risk identification and management, status tracking, internal and external stakeholder management etc. Act as primary point of contact within CDM for any HA submission related activities (e.g. preparation of briefing books, attending HA meetings as request. 

Who you are:

• Minimum of 10 years of experience in clinical data management within the pharmaceutical, biotechnology, or healthcare industry
• Committed to continuous personal and professional development, and bringing external insights to the role to drive innovation and process improvement
• Proficient in contributing to non-study related initiatives e.g. process improvements, in addition to study assignments 
• Strong project management, analytical, communication, collaboration, and problem-solving skills
• Demonstrated ability to lead and oversee end-to-end data management activities within a clinical trial, as well as leading and coordinating global teams in a matrix organization
• Familiar with autonomously providing reports to senior management, including updates on financials, forecasts and timelines
• Experience in Risk Based Data Monitoring/Management, and with clinical trial data standards, such as CDISC, is preferred
• Bachelor's or Master's degree in a scientific or technical discipline, preferably in life sciences, data management, or a related field

Your main benefits:

• Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card  
• Work-Life balance: Enjoy additional paid days off, flexible working hours.
• Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
• Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.

Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal.