Local Study Associate Director - Sao Paulo, Brasil - AstraZeneca

AstraZeneca

Empresa verificada

Sao Paulo, Brasil

há 1 semana

Postado por:

Ana Silva

beBee Recruiter

Descrição

AstraZeneca is one of the most fascinating biopharmaceutical companies in the world.

From researchers to sales people, from lab technicians to the legal department, we all have a mission to turn ideas into science, science into revolutionary medicines that save and extend patients'; lives and benefit society.

Our portfolio is solid and our pipeline is innovative with a focus on biological medicines in the Cardio-Metabolic, Respiratory and Oncology areas.

Main accountabilities:

Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality.
Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies
Leads and optimises the performance of the Local Study Team(s) at country level ensuring compliance with AZ Procedural Documents, ICH-GCP and local regulations.
Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality.
Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks.
Ensures timely preparation of local Master CSA (including site budget) and amendments as needed.
Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant AZ SOPs and local regulations.
Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with AZ SOPs.
Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction).
Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations.
Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans.
Reviews monitoring visit reports (as required and following AZ SOPs) and proactively advices the monitor(s) on study related matters.
Performs any required comonitoring, Accompanied Site Visits/training visits with study CRAs.
Proactively identifies risks and facilitates resolution of complex study problems and issues.
Organises regular Local Study Team meetings on an agenda driven basis.
Actively works towards achieving good personal relationships with all Local Study Team members, sites' staff and global stakeholders.
Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead.
Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary.
Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed.
Communicates and coordinates regularly with National Coordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable.
Plans and leads National Investigator meetings, in line with local codes, as required.
Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies.
Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are setup, updated and access is organised at country level.
Ensures accurate payments related to the study are performed according to local regulations and agreements.
Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and AZ Procedural Documents.
Ensures completeness of the eTMF and ensures essential documents are uploaded in a timeline manner to maintain the eTMF "Inspection Ready".
Ensures that all study documents are ready for final archiving and completion of local part of the eTMF.
Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA.
Provides input to process development and improvement.
Provides regular information to Line Managers at country level on study/ies and planned study milestones/key issues.
Updates Line Managers about the performance of the CRAs/CSAs.
Ensures that study activities at country level comply with local policies and code of ethics.
Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market.
Ensures compliance with AstraZeneca's Code of Ethics, company policies and procedures relating to people, finance,