DIRECTOR STUDY MANAGEMENT HAEMATOLOGY

Location.
Barcelona, Spain (On-site) / 3 days working from the office and 2 days working from home.
The DSM, is responsible for leading, developing, supporting, and providing direction to Study   Management and Operations (SMO) personnel for project, TA/scientific/technical, and operational   related issues to enable delivery of drug projects and non drug projects.
The DSM is ac countable for   resourcing SMO members o n study teams to support delivery of clinical programs in R&D.
The role   holder will also be responsible for embedding consistent ways of working across Hubs and building   SMO capabilities.
The DSM will ensure that direct reports are equipped with the right skills and capabilities to   successfully lead and deliver clinical trials.
Take responsibility and act as a change agent to drive   consistent implementation of globally agreed Clinical Operations and Clinical Development strategies including processes and technology related to the delivery of studies.
Line management of SMO staff   Recruit, Retain & Develop SMO personnel.
Demonstrate AZ values.
Facilitate skills and capability training to SMO personnel to support their development.
Ensure personnel have been trained and work within compliance of ethics, company policies and standard procedures.
Role model and embed a performance driven culture and coach staff for optimum performance.
Develop and nurture capabilities of our present and future AZ leaders.
Manage performance including feedforward and rewards.
Provide expertise and direction to support direct reports with proactive problem/risk          identification, solution building and issue resolution to facilitate achievement of objectives on time a       and to appropriate quality.
Delivery of projects   Maintain dialogue with Senior DSM and Snr Global Clinical Operations Program Director to anticipate project requirements and mitigate risks to project delivery.
Allocate appropriately skilled SMO personnel to study delivery teams to ensure delivery of clinical studies to time, budget and quality standards in accordance with clinical performance targets.
E nsure staff understand global project priorities and specific project challenges.
s upport staff/team to achieve project milestones and study deliverables.
T o work across departments to support the delivery of projects and organizational improvements.
Hub Leadership   Participate in setting, and responsible for implementing, the vision & strategy for the SMO Hub, aligned with Clinical Operations and Hematology’s Vision & Strategy.
Contribute to business strategy and streamline processes for drug/non-drug projects or departmental activities.
Lead and support change by encouraging diversity of solutions and implementing process   changes consistently across SMO.
Act as a change Agent, with local and global impact, to ensure adoption of Global initiatives.
Promote and encourage innovation and creativity.
Work with Leadership team and Global Study Leads to achieve accurate resource forecasting and develop solutions to efficiently and flexibly resource study teams.
Promote and encourage communication within and across Hubs and between BioPharma and Oncology SMO.
Ensure quality and compliance to External Regulations and AZ Standards.
Work across the Hubs to develop global efficient ways-of-working.
Provide expert input into functional and cross-functional global processes.
Provide leadership in local Hub.
Foster the sharing of study delivery knowledge, information, and best practice on individual performance to the study team members and their line managers to support their professional development; may mentor less experienced colleagues.
E ducation, Qualifications, Skills and Experience Essential.
Bachelor’s degree required, preferably in medical or biological science, or related subject or equivalent qualification or experience.
Experience in the   pharmaceutical industry.
Comprehensive experience of clinical and Drug.
Development process within a pharmaceutical or clinical background.
Proven leadership and ability to promote motivation and empower others in order to accomplish individual, team and organizational objectives.
Thorough knowledge of Study Management processes in both local regulation and global environment.
An understanding of Oncology/Hematology TA.
Strong leadership, problem solving, stakeholder management and conflict resolution skills.
Ability 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 add value to the business.
Demonstrated ability to set and manage priorities, resources, performance targets and project initiatives in a global and regional environment.
Excellent written and verbal communication   skills, negotiation, collaboration and interpersonal skills.
Desirable.
Advanced degree in a scientific discipline.
Line management experience.
Expert reputation within the business and   Industry.
Extensive knowledge of the latest technical information.
Ability 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 comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.