Location: Barcelona, Spain (on-site)
Able to be office based (3 days per week) in the Barcelona office from day 1.
The Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of flexibility is required.
Typical Accountabilities Contribute to the development of study documents as appropriate as well as any updates/amendments, ensuring template and version compliance.Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable country documents.Manage the set-up of third-party vendors assessing initial statement of work and budget, as well as the change order process.Provide input to data management documents (e.g. Case Report Form, Data Validation Specifications), and collaborate with data management representatives and sites to facilitate the delivery of study data.Initiate contract/budget requests and track ongoing status; facilitate generation of purchase orders, review vendor invoices and assist in tracking spend against approved budget.Ensure the supply of Investigational product and study materials by liaising with Drug Supply or external service providers as appropriate.Oversight of third party vendors, global / local internal staff and investigator sites to support effective delivery of a study and its regulatory documents from development of the protocol through to the Clinical Study Report.Provide oversight of and support recruitment and data delivery as well as risk mitigation strategies.Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates.Monitor study conduct and progress, proactively identifying and resolving issues which may impact delivery of the study to the necessary quality, timelines or budget.Support risk management and quality efforts to ensure study compliance.Support set-up, maintenance, closeout and archiving of the Trial Master File (TMF), ensuring continual inspection readiness.Prepare presentation material for meetings, newsletters and websites.Support the study team in the implementation of audits and regulatory inspections.Contribute to review of new/amended/unique SOPs and guidance documents.Education, Qualifications, Skills and Experience University degree / Bachelor's degree, preferably in medical or biological science, or field associated with Clinical Research, or equivalent experienceMinimum of 3-4 years of progressive clinical trial experienceExperience of working with and delivering through strategic partners and 3rd party vendorsExcellent knowledge of ICH-GCP principlesTeam orientatedAbility to coordinate and prioritise multiple tasks and resultsProactive approachHigh degree of flexibilityProven verbal and written communication skillsGood negotiation and collaboration skillsProven interpersonal and problem-solving skillsSome travel may be requiredFluent in English (verbal & written). Able to present optimally.CV in English is needed. Maximum 2 pages.Cover letter in English is needed. Following information should be included in the cover letter:Why are you interested in this AZ posted job and what value will you bring to your AZ Team?Which are your: Top-3 career achievements & Top-3 learned lessonsCandidates have to complete Workday profile. Minimum salary expectations in Euros is required in all cases.Early phase oncology clinical trial experience
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