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ASSOCIATE DIRECTOR CLINICAL STANDARDS

Barcelona - Barcelona

Descripción de la oferta de empleo

Join us as an Associate Director Clinical Standards, where you will be accountable for leading, managing, and developing a team of clinical data standards developers.
This role presents an opportunity to showcase your department mindset and management skills in overseeing the scope and complexity of clinical data standards in raw data collection and cleaning components packages.
As a recognized expert within your field, you will often be the first point of contact for related queries, act as a coach or mentor for staff, and act as a specialist within cross-functional teams to deliver continuous improvement.
Accountabilities.
In this role, you will lead clinical data standards developers and act as a technical subject matter expert in specialized areas of clinical data standards data collection and cleaning components.
You will manage activities of our CRO partners and external partners, lead the quality of your own deliverables and oversee the quality of other developers' standards deliverables.
You will also drive standards development and implementation within the business, contribute to function recruiting, training, and mentoring, and represent Clinical Data standards at cross-functional forums and meetings.
Essential Skills/Experience.
- BSc in Information Sciences, Mathematical, Statistical, Computer Science or Life Science or equivalent experience.
- Expertise in specialized standards development skills (eg, raw data standards with data collection and cleaning components, clinical coding dictionaries, and data analysis & reporting standards (SDTM, ADaM, TFLs)) or expertise in Biometrics functions (eg, Data Management, Programming, or Statistics) - Excellent knowledge of industry standards (eg, CDASH, SDTM, ADaM) - Ability to apply standards expertise to problem - Excellent communication skills in both written and spoken English  - Strong project management skills     - Ability to mentor, train and lead teams - Thorough knowledge of the clinical development process - A clear demonstration of behaviours of truth seeking rather than success seeking - Agile responsiveness to industry and business needs - Embracing of peer review Desirable Skills/Experience.
- Understanding of programming languages (eg, SAS, R, Java, Groovy, Spotfire, C/C++, VBA/VBS,.
ET, Python, Pearl) - Ability to influence relevant stakeholders on standards related items - Ability to manage risk - Ability to line manage When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines.
In-person working gives us the platform we need to connect, work at pace and challenge perceptions.
That's why we work, on average, a minimum of three days per week from the office.
But that doesn't mean we're not flexible.
We balance the expectation of being in the office while respecting individual flexibility.
Join us in our unique and ambitious world.
At AstraZeneca's Biopharmaceuticals R&D division, we are driven by our desire to understand and reveal new insights.
We are free from fear of failure and are encouraged to ask the right questions and make bold decisions.
We take inspiration from within our BioPharmaceutical heritage and beyond.
Our leaders inspire us by engaging others, building compelling cases and sharing our ideas for change.
We are committed to making an impact on patients' lives by improving patient access to healthcare globally.
Our values guide everything we do at AstraZeneca.
They power our belief in What Science Can Do - a belief in its potential to redefine what's possible.
Are you ready to explore and innovate in our dynamic environment? Be encouraged and supported to think creatively.
Here we are free from fear of failure, free to ask the right questions and make bold decisions.
It takes resilience to embody our entrepreneurial spirit.
For those who thrive on experimentation, you'll get to work with knowns and unknowns.
Exploring without limits.
Apply now! AstraZeneca embraces diversity and equality of opportunity.
We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.
We believe that the more inclusive we are, the better our work will be.
We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.
We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
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Detalles de la oferta

Empresa
  • Associate Principal Clinical Data Manager
Localidad
Dirección
  • Sin especificar - Sin especificar
Tipo de Contrato
  • Sin especificar
Fecha de publicación
  • 17/09/2024
Fecha de expiración
  • 16/12/2024
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