Director, Clinical Data Management

hace 2 semanas

Madrid, España Caidya A tiempo completo

We're seeking a Director of Clinical Data Management to join our team working remotely from any UK location — this pivotal role focuses on delivering the highest quality data management support. You will lead teams encompassing technical consulting, seamless client interface, and operational excellence. You'll be the face of our data management team, guiding project teams and fostering communications across our global offices. Your expertise will support our Business Development team, crafting proposals and budgets and elevating client presentations with your professional acumen.

You’ll possess an excellent understanding of Data Operations, superb organizational skills, and the capability to navigate the complexities of clinical research. Leadership is second nature to you, demonstrated through your ability to inspire teams in various settings, including remote and international projects.

Your mission will be to ensure the integrity and quality of data, leading by example and fostering a culture of excellence. With a dedicated home office, you'll thrive in a flexible environment that champions innovation and improvement.
**Job Title**:Director, Clinical Data Management**Job Location**: Remote-based position (Spain)**Job Overview**:
Provision of highest-quality data management support in the form of technical/consulting support, client interface and operational management.

**Job Duties and Responsibilities**:
The specific job duties of a Director, Clinical Data Management include those of Manager, Clinical Data Management and may include but are not limited to:

- Represents the data management organization including attendance at professional meetings and provides direction for project teams.
- Supports communication between the regional and international offices on Data Management and related issues.
- Supports the Business Development team with business development activities in relation to Data Management services, including proposal and budget input/development and client presentations.
- Represents the company with professionalism at every opportunity.
- Provides guidance and oversight of data management activities as required.
- Supports the Project Managers and Project Team in the delivery of high-quality DM services.
- Advise upon, negotiate and coordinate timelines for the completion of data management projects.
- Provides technical advice and support in all matters related to data management, including support with client and project discussions.
- Implement adequate data quality control measures.
- Identify and address problems. Seek to understand all contributing factors. Propose, implement, and evaluate appropriate solutions.
- Plan budget of the department and track budget adherence in cooperation with Financial Controlling.
- Allocation of internal and external resources to projects in cooperation with the Project Manager.
- Recruitment of new department members in cooperation with Human Resources.
- Conduct internal and external team meetings as necessary.

**Supervisory Responsibilities**: This job involves supervisory responsibilities for other employees or contractors, which may include:

- Clinical Data Manager (I, II or Senior)
- (Senior) Manager, Clinical Data Management
- Manager, Coding
- Coding Specialist

**Job Requirements**:
**Education**:

- Master’s degree in life science, computing, nursing qualification or other equivalent experience or education e.g. Laboratory experience.

**Experience**:

- Minimum of 8 years of experience working in the field of data management, biostatistics or related areas.
- Experience working in pharmaceutical and/or Contract Research Organization (CRO) industry preferred.
- High-level technical understanding of Data Operations services and delivery methods essential.
- Experience working in a home office environment, as applicable.
- Experience of working internationally an advantage.
- Leadership - successful experience of team leadership roles in a variety of scenarios, including functional management, matrix management and international or multi-site environments.

Skills/Competencies:

- Excellent organizational skills.
- Strong written and verbal communication skills.
- Exceptional attention to detail.
- Knowledge of clinical research including regulatory requirements GCP/ICH.
- Knowledge of activities of other functions in performing clinical trials.
- Strong interpersonal skills.
- Strong computer skills, including Microsoft Office and clinical data management systems.
- Able to exercise judgment within defined procedures and practices and to determine appropriate action independently.
- Superior problem-solving, decision making, planning and delegation skills.
- Mature management skills demonstrated by calm and thorough review of situations.
- Ability to lead in pursuing improvements.

Capabilities:

- Flexibility - willing to change assignments and work focus to accommodate project demands.
- Dedicated home office environment for f

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