Director Study Operations - Cardiovascular, Renal And Metabolism

Director Study Operations - Cardiovascular, Renal And Metabolism
Empresa:

Astrazeneca Gmbh


Detalles de la oferta

Location: BarcelonaJoin us as a Director of Study Operations in our Biopharmaceuticals R&D department. In this role, you will be responsible for leading, developing, supporting, and providing direction to Study Management personnel to enable the delivery of drug projects and non-drug projects. You will be accountable for resourcing Study Management members on study teams to support the delivery of clinical programs. This role is an opportunity to embed consistent ways of working across locations and build Study Management capabilities.Typical Accountabilities:1- Line management of Study Management Late staffRecruit, Retain & Develop personnelDemonstrate AZ valuesProvide skills and capability training to personnel to support their developmentEnsure personnel have been trained and work within compliance of ethics, company policies and standard proceduresRole model and embed a performance driven culture and coach staff for optimum performanceDevelop and cultivate capabilities of our present and future AZ leadersHandle performance including feedback and rewardsProvide expertise and direction to support direct reports with proactive problem/risk identification, solution building and issue resolution to facilitate achievement of objectives on time and to appropriate qualityTimely assignment of capable Study Management resources to meet the clinical study team demands, in collaboration with other members of Study Management Leadership team, and the Capacity Management Team2- Study ManagementParticipate in setting, and responsible for implementing, the vision & strategy for the Study Management, aligned with BioPharmaceuticals ClinicalVision & StrategyContribute to business strategy and streamline processes for drug/non-drug projects or departmental activitiesLead and support change by encouraging diversity of solutions and implementing process changes consistently across Study ManagementAct as a change Agent, with local and global impact, to ensure adoption of global initiativesPromote and encourage innovation and creativityWork within Study Management to achieve accurate resource forecasting and develop solutions to efficiently and flexibly resource study teamsPromote and encourage communication within and across Study Management and BioPharmaceuticals ClinicalEnsure quality and compliance to External Regulations and AZ StandardsWork across the locations to develop global efficient ways-of-workingProvide guide into functional and cross-functional global processesFoster the sharing of study delivery knowledge, information, and best practiceEssential requirements:Bachelor's degree required, preferably in medical or biological science, or related subject or equivalent qualification or experience.10 or more years of experience in the pharmaceutical industryComprehensive experience of clinical and Drug Development process within a pharmaceutical or clinical backgroundProven leadership and ability to promote motivation and empower others in order to accomplish individual, team and organizational objectivesThorough knowledge of Study Management processes in both local regulation and global environmentAn understanding of the therapeutic areas related to AstraZeneca's productsStrong leadership, problem solving, stakeholder management and conflict resolution skillsAbility to lead change with a positive approach to the challenges of change for self, team, and the business. Sees change as an opportunity to improve performance and make valuable contributions to the businessDemonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a global and regional environmentExcellent written and verbal communication skills, negotiation, collaboration and interpersonal skillsDesirable requirements:Advanced degree in a scientific disciplineLine management experienceExpert reputation within the business and industryExtensive knowledge of the latest technical informationAbility to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.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 follow all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.At AstraZeneca, we follow the science to explore and innovate. We are working towards treating, preventing, modifying and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference. We have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.Are you ready to embrace new and varied opportunities to develop and learn? Join us today!#J-18808-Ljbffr


Fuente: Allthetopbananas_Ppc

Requisitos

Director Study Operations - Cardiovascular, Renal And Metabolism
Empresa:

Astrazeneca Gmbh


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