Manager, Clinical Data Management

Data Management Leadership

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Summary:

To provide management and leadership oversight of assigned teams and projects within Data Management department for study execution and budget management. Support development and implementation of Worldwide processes and initiatives.

• Provide management and leadership oversight of teams and projects within Data Management department for study execution and budget management.
• Act as the primary point of contact for any study specific escalations (internal or external).
• Represent the company at sponsor governance meetings.
• Manage assigned departmental personnel ensuring: staff are allocated to projects appropriately and according to their abilities/competencies; appropriate oversight, training and mentoring is provided; projects within the team are appropriately resourced; operational or budget risks are discussed and addressed; any performance related escalations for team member are managed and handled appropriately; highlight upcoming availability to DM Management to ensure continuity of utilisation;
  
  define and monitor objectives for individual team members, ensuring there are opportunities for career and personal development.
• Provide support to Business Development staff by participating in preparation of proposals and presentations to sponsors.
• Participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings. Ensure that any recommendations are discussed and that solutions are incorporated.
• Perform the role of Subject Matter Expert for a specific DM process: ongoing review to ensure the process is effective and efficient; central point of contact for any related questions from the team; provide ongoing training to all team members; take ownership of any related Quality Issues identified, ensuring root cause analysis and CAPAs as required; ownership and regular updates of related QMDs or other guidance documents;
  
  provide mentorship to other members of the DM department; lead and manage departmental initiatives for process improvement and efficiencies as defined by the DM Departmental leadership.
• Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

• Excellent attention to detail.
• Excellent written and verbal communication skills.
• Expert knowledge of data management best practices & technologies as applied to clinical trials.
• Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams.
• Advanced understanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
• Independent analytical and problem solving skills.
• Strong project management skills and experience managing data management teams and projects for operational and budget oversight.
• Line management experience including recruitment, career development and performance reviews.

• Bachelor's degree or higher in biomedical sciences, life sciences,…