Primary accountability:

Quality and timeliness of study deliverables (site identification, feasibility, start up, recruitment, data deliverables, filing of complete study documentation) for assigned study(ies)Proactive reporting of study-specific issues (including monitoring metrics) to the study team via the Study Lead Country Operations (SLCO)Quality of monitoring oversight in the country for assigned study(ies)Meeting recruitment targets for assigned study(ies)CDA delivery and negotiation (based on pre-approved parameters and regardless of executory party)Negotiation of site study budgetsOversight of FSP and /or contingent workers on assigned study(ies)Review if local regulatory documentation and oversight of local regulatory activitiesRelationship management with the national coordinating investigator as applicable

Primary responsibility:

Timely and accurate responses to queries from the study teamWorking with Medical Affairs to coordinate site feasibility and engagement activitiesScheduling and leading effective country calls with local study team and/ or CROResolving ICF issues in countryOversight of EC submissions and facilitate resolution of queriesProposing potential investigator sites (HCO accountable for selection)Conduct trainingof CRAsReview Clinical Monitoring DocumentationInspection readiness activitiesRelationship management with sitesProvide feedback to Internal and External Stakeholders as appropriateDevelop and maintain tracking toolsDrives quality efforts to proactively identify and manage risks to study quality

Qualifications

Proven experience in the oversight and delivery of operational aspects of all stages of of clinical trial processSolid knowledge of clinical development processesAbility to lead, troubleshoot and influence for quality and deliveryA track record of ensuring GCP compliance and successful risk management of complex clinical studies is expectedProven experience in effectively communicating with site staff including and including KOLs and thought leadersComprehensive and current regulatory knowledge, including GCPExperience conducting GCP or other training is a plusDemonstrates flexibility in schedule and willingness to travel (required travel may be as high as 20% during busy periods)Good organizational skills and ability to deal with competing prioritiesEffective communication skills (written, verbal and presentation)Creative thinker, curious and unafraid to ask questionsInnovator, willing to initiate changes, introduce new ideas, and creatively problem solveProficient with MS Office Suite (Excel, Word and PowerPoint). 

Preferred Qualifications

Bachelor's Degree or equivalent in one of the disciplines related to clinical practice/health care, life sciences or drug development is required.  A clinical or advanced degree (RN, MPH, MS, MA, MBA, PharmD,) is preferred.8+ years of relevant experience gained with a CRO or pharmaceutical company working on multinational clinical studies; Lead CRA/management experience preferredProven experience in managing high priority / complex studies through phases 1 – 4 and in rare medical conditions preferredPrevious oversight and regulatory inspection experience preferred

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.