Associate Director, Clinical Data Management

3 weeks ago

Nottingham, United Kingdom Worldwide Clinical Trials Full time

**Requisition Number**7869**

**Employment Type**:Regular**

**Who we are**

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

**Why Worldwide**

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us

**What Global Data Management does at Worldwide**

Data Management is an ever growing and collaborative department. Our global team is a group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies beginning with building the study database, to locking and delivering the final dataset for the project. Data Management reviews and ensures the clinical study data is of high quality for regulatory submissions.

The Data Management group is the perfect place to launch or further your career. Whether it is technical expertise, or coming from a clinical background, you’re able to hone and expand your skillset within our department. Spanning various roles from data support staff, database and SAS programmers, coders and functional leads, there is place for you

**What you will do**
- Lead and manage staff performing Data Management and Data management database development. Develop staff members, including the performance of staff appraisals and continued management
- Contribute to the strategic management of the department. Liaise with others to coordinate project specific development activities
- Ensure that all operations carried out by department are conducted to applicable regulations, GCP, WCT SOPs and guidelines, and to the requirements of the sponsor
- Monitor project progress, assess work against contract, identify and report out of scope work and assist with costs estimates for proposals as well as change orders
- Lead and manage the development of new processes

**What you will bring to the role**
- Previous Lead clinical data management experience gained within clinical research
- Excellent working knowledge of clinical data management systems and principles
- A good standard of written and spoken English
- Excellent time management skills with ability to work to and direct project plans
- Ability to prioritize and handle multiple projects simultaneously; flexible and able to use sound independent judgment and take initiative to assess information
- Proven leadership and management skills

**Your experience**
- Educated to degree level, together with relevant technical experience or with extensive relevant technical experience
- Clinical drug development experience including experience in Clinical Data Management
- Excellent written and verbal communication skills and strong attention to detail are essential
- Good knowledge of guidelines and regulations relevant to the deployment and use of technologies in clinical development programs

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