Clinical Research Associate ll Oncology (Remote Oregon)

The CRA II advances AbbVies pipeline by striving for excellence in clinical research turning science into medicine for patients and leveraging advanced capabilities to drive industry-leading performance.The CRA II partners with investigators and site staff to build meaningful effective engagements that position reputed company as the sponsor of choice in clinical trials.The role focuses on site clinical research by ensuring proper trial conduct while continually working to improve data reputed company compliance overall study performance and the customer experience.Responsibilities :Considered as the primary reputed company of contact for the investigative site.High level of competency or experience in providing contextual information on the clinical trials connects stakeholder to the investigative sites and strengthens AbbVies positioning.Aligns trains and motivates the site staff and principal investigator on the goals of the clinical trial program protocol and patient treatment principles for the trial ensuring a trusted partnership.Conducts site evaluation site training routine and site closure monitoring activities with compliance to the protocol and monitoring plans in accordance with applicable regulations Good Clinical Practices (GCPs) ICH Guidelines reputed company Standard Operating Procedures (SOPs) and quality standards ensuring safety and protection of study subjects.Advanced understanding of site engagement and ability to customize site engagement strategy for assigned study (ies).Gather local / site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool to report / track reputed company and measure impact of that strategy.Advanced level of competency connecting the study protocol scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities.Evaluate and ensure effective recruitment and retention techniques / plans based on the patient disease journey.reputed company solid knowledge of therapeutic area asset and clinical landscape / patient journey to reputed company successful patient recruitment and overall protocol compliance.Possesses reputed company level of competency to mentor and train less reputed company CRAs on various aspects of work and provides input into their development.May participate in global / local task forces and initiatives.Responsible for activities as assigned by manager.Responsible for reputed company risk-assessment proactively and in collaboration with Central Monitoring team monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues.Advanced ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution.Ensures preventative and corrective action plans are put into reputed company as needed to mitigate risk and promote compliance using a customer centric approach.Identifies evaluates and recommends new / potential investigators / sites on an on going basis.Potential sites may be identified through networking or internal reputed company requests to assist in the placement of planned clinical studies with qualified investigators.Ensures quality of data submitted from study sites and assures timely submission of data including appropriate reporting and follow-up for reputed company safety events by site personnel.Ensures audit and regulatory inspection readiness at assigned clinical site at reputed company times.Manages investigator payments as per executed contract obligations as applicable.Qualifications :Minimum Qualifications :Minimum of 1 year of clinically reputed company experience of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials.(CRA experience)Familiar with risk-based monitoring approach onsite and offsite monitoring.Preferred Qualifications :Appropriate tertiary qualification in health reputed company disciplines (Medical Scientific Nursing) preferred.Knowledge of appropriate therapeutic area indications (oncology) is preferred with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials.Experience as a study coordinatorOther Required Skills :Advanced knowledge on existing and emerging local regulatory and legal requirements ICH / GCP Guidelines and applicable policies.Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.Demonstrate strong planning and organizational skills and the ability to work effectively and reputed company in a dynamic environment with competing projects and deadlines.Advanced ability to reputed company technology tools and resources to provide customer centric support based on the health of the site.Strong interpersonal skills with excellent written verbal active listening and presentation skills with ability to establish and reputed company site relationships and t