Clinical Research Associate

About AstraZenecaAstraZeneca is a global science-led patient-focused biopharmaceutical company that focuses on the discovery development and commercialization of prescription medicines for some of the worlds most serious diseases But were more than one of the worlds leading pharmaceutical companies The Clinical Research Associate CRA has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team s The CRA works in close collaboration with other CRAs and the Local Study Team Local Study Associate Director LSAD to ensure that study commitments are achieved in a timely and efficient manner The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study The CRA is responsible for the preparation initiation monitoring and closure of assigned sites in clinical studies in compliance with AZ Procedural Documents international guidelines such as ICH-GCP and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies A CRA with longer tenure and experience may take on additional responsibilities that include additional tasks associated with LSAD CRAs might have different internal titles based on the experience level CRA Senior CRA The experience level depends on the years of experience performance record level of independence in the role ability to take on additional tasks or tutor more junior colleagues The Director Country Head may assign this internal title after confirmation with Senior Director Cluster Head or Executive Director Regional Head Typical Accountabilities Contributes to the selection of potential investigators In some countries as required CRAs are accountable for study start-up and regulatory maintenance Tasks may include Site Qualification Visits collection preparation review and tracking of documents for the application process submission of proper application documents to EC IRB and to Regulatory Authorities for start-up and for the duration of the study Trains supports and advises Investigators and site staff in study related matters including Risk Based Quality Management RbQM principles Confirms that site staff have completed and documented the required trainings appropriately including ICH-GCP training prior to and for the duration of the study Ensures the sites are inspection ready at all times Actively participates in Local Study Team LST meetings Contributes to National Investigators meetings as applicable Initiates monitors and closes study sites in compliance with AZ Procedural Documents Shares information on patient recruitment and study site progress site quality performance within the LST Drives performance at the sites Proactively identifies and ensures timely resolution to study-related issues and escalates them as appropriate Updates CTMS and other systems with data from study sites as per required timelines Manages study supplies ISF etc drug supplies and drug accountability at study site Prepares study drug for destruction if applicable Performs monitoring visits remote and onsite as well as remote data checks in accordance with the timelines specified in the study specific Monitoring Plan If required determines and discusses with LSAD the correct timing and type of visits Performs Source Data Review SDR Case Report Form CRF review and Source Data Verification SDV in accordance with the Monitoring Plan Performs regular Site Quality Risk Assessments and adapts monitoring intensity accordingly during the study Ensures data query resolution in a timely manner Works with data management to ensure robust quality of the collected study data Ensures accurate and timely reporting of Serious Adverse Events and their follow ups Prepares and finalises monitoring visit reports in CTMS and provides timely feed-back to the Principal Investigator including follow-up letter within required timelines and in line with AZ SOP Follows up on outstanding actions with study sites to ensure resolution in a timely manner Follows quality issue processes by escalating systematic or serious quality issues data privacy breaches CSP or ICH-GCP compliance issues to Local Management and or CQM as required Assists site in maintaining inspection ready ISF Prepares for and collaborates with the activities associated with audits and regulatory inspections in liaison with LSAD and CQAD Ensures timely collection uploading of essential documents into the eTMF in accordance with ICH GCP AZ SOPs and local requirements Supports participates in regular QC checks performed by LSAD or delegate Ensures that all study documents under their responsibility i e site documents relevant communications etc are available and ready for final archiving and completion of local part of the eTMF Provides feedback on any research related information including sites investigators competing studies that might be useful for the local market Ensures compliance with AstraZenecas Code of Ethics company policies and procedures relating to people finance technology security and SHE Safety Health and Environment Ensures compliance with local national and regional legislation as applicable Collaborates with local MSLs as directed by LSAD or line manager Education Qualifications Skills and ExperienceEssential Bachelor degree in related discipline preferably in life science or equivalent qualification Excellent knowledge of international guidelines ICH-GCP basic knowledge of GMP GDP Good knowledge of relevant local regulations Good medical knowledge and ability to learn relevant AZ Therapeutic Areas Basic understanding of the drug development process Good understanding of Clinical Study Management including monitoring study drug handling and data management Excellent attention to details Good written and verbal communication skills Good collaboration and interpersonal skills Good negotiation skills Ability to travel nationally internationally as required Ability to work in an environment of remote collaborators Manages change with a positive approach for self team and the business Sees change as an opportunity to improve performance and add value to the business Ability to look for and champion more efficient and effective methods processes of delivering quality clinical trials with reduced budget and in less time Desirable Good analytical and problem-solving skills Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines Familiar with risk-based monitoring approach including remote monitoring Good cultural awareness Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems software in an e enabled environment Team oriented and flexible ability to AstraZeneca Internal Site Management Monitoring Clinical Research Associate Why AstraZenecaAt AstraZeneca were dedicated to being a Great Place to Work Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit Theres no better place to make a difference to medicine patients and society An inclusive culture that champions diversity and collaboration and always committed to lifelong learning growth and development Were on an exciting journey to pioneer the future of healthcare Date Posted 16-May-2025Closing Date 29-Jun-2025AstraZeneca 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