Detalles del empleo
Tipo de empleo: Jornada completa Ubicación: 08028 Barcelona, Barcelona provincia Descripción completa del empleo:
Location: Barcelona, Spain (On-site) / 3 days working from the office and 2 days working from home.
The Global Study Director (GSD) is a business-critical role within the Haematology organisation whose main accountability is the operational planning and delivery of high priority and complex clinical studies within a program, or across programs that are deemed most critical to the business. The GSD is responsible for the delivery of clinical studies, including quality, timelines, budgets, resources, investigational sites, vendors and key project deliverables in compliance with SOPs, Regulatory requirements and ICH/GCP guidelines.
The GSD leads a cross-functional study team (core and extended) and provides the team with direction and guidance to enable successful study delivery. The GSD may provide input to early study planning activities based on operational expertise. The GSD is accountable to the CPT for the delivery of a study, or studies, according to agreed upon timelines, budget and quality standards by ensuring an effective partnership and teamwork within the study team. The GSD will also interface with other internal stakeholders cross-functionally, and/or external partners, to identify, manage and resolve issues affecting study delivery.
Typical Accountabilities:
Lead and coordinate a cross-functional study team of experts in accordance with SDO/STOM and its roles, accountabilities and responsibilities framework (RACI) to ensure the clinical study progress as planned driving achievement of milestones according to timelines, budget and quality standards.Contribute to vendor/ESP selection activities at the study level, including bid defense, and lead operational oversight at the study level in order to ensure appropriate control over the vendor identification and selection.Assist the (Sr)GPD with the operational planning for upcoming clinical studies to establish required number of resources for study conduct, interfacing with other cross-functional partners and the TA as required.Collaborate with other functions to establish strategies and identify synergies aimed at increasing efficiency of global study teams (core and extended).Lead and facilitate communication across functions and provide guidance and support to the core and extended study team members as needed and in accordance with study-specific communication plan.For outsourced studies, be the primary AZ point of contact for the CRO Study Manager to ensure study delivery according to agreed upon timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, in accordance with relevant AZ SOPs and guidelines.Provide operational expertise into and hold accountability for the development of essential study level documents (i.e. Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)) in accordance with relevant AZ SOPs.Ensure all external service providers (i.e. central laboratories, IXRS, ePRO, etc.) engaged at the study level are performing to contracted goals and timelines/budget and that adequate oversight is documented through planning & control activities.Develop and maintain relevant study plans (e.g. global study management plan and its relevant components such as study project plan SPP) including required input into study level quality and risk management planning (e.g. risk-based quality management, proactive risk and contingency plans, etc.), ensuring that the risk response strategies and issue escalation pathways are clear to the entire study team.Oversee study level performance against agreed upon plans, milestones and key performance indicators (KPIs, quality and operational) by using company tracking systems and project timelines (e.g. SPP, data flow metrics dashboard, CTMS or eTMF dashboard) and communicate any risks to timelines and/or quality to CPT, along with proposed mitigations.Identify and report quality issues that have occurred within the study in accordance with relevant AZ SOP and collaborate with all functions as necessary to overcome barriers and achieve milestones; proactively communicate findings and corrective action plans (CAPAs) to relevant stakeholders (e.g. CPT, quality assurance staff, functional line management, etc.).Oversee Trial Master File (TMF) completion in accordance with relevant AZ SOPs, including ensuring the TMF plan and Expected Document List (EDL) are in place and that QC activities are performed on an ongoing basis to ensure TMF completeness at all times.Ensure timely compliance with company-wide governance controls (e.g. Delegation of Authority, Sunshine Act, ACCORD attestations, Clinical Trial Transparency).Responsible for study budget re-forecasting following initial budget estimate provided by the CPT and accountable for study budget management through the study lifecycle and for providing budget progress reports to the CPT including any financial risks and mitigation plans (as part of the ongoing study change control process).Ensure studies are inspection-ready at all times, according to ICH-GCP and AZ SOP and relevant policies/guidelines.Supports professional development of team by providing regular feedback on individual performance to the study team members and their line managers.Provide guidance, training, expert input, mentoring and support to less experienced GSL colleagues on an ongoing basis.Leads non-drug project work such as SMO/Haematology representative in process improvements and/or leading improvement projects as discussed and agreed upon with their manager.Leads program level projects/initiatives as discussed and agreed upon with their manager.Education, Qualifications, Skills and Experience:
Essential: University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research.Proven project management experience and training.At least 7 years of clinical trial experience.At least 3 years of experience in global study leadership and team leadership.Demonstrated clinical trial expertise in Haematology and/or Oncology.Extensive knowledge of ICH-GCP guidelines and clinical research regulatory requirements and experience in all phases of clinical study delivery; startup, maintenance and close out.Thorough understanding of the cross-functional clinical trial process eg. Data flow.Strong strategic and critical thinking abilities.Proven skillset and abilities in complex problem solving and decision-making.Strong abilities in establishing and maintaining effective working relationships with senior stakeholders, along with strong conflict management skills.Demonstrated abilities in mentoring.Excellent communication and interpersonal skills.Ability to manage multiple competing priorities.Experience in external provider oversight and management.Desirable: Advanced degree, Masters level education (or higher).Project management certification.5 years of experience in global study leadership and team leadership.Significant Haematology/Oncology expertise.Expertise in different phases of a clinical delivery.Experience with Project Management software solutions.
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