Clinical Research Associate ll - Oncology (Remote - Oregon)

Company Description reputed company's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of reputed company. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about reputed company, please visit us at www.reputed company.com. Follow @reputed company on X, Facebook, Instagram, YouTube, reputed company and Tik Tok.

Job Description

The CRA II advances reputed company's 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 reputed company's 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 coordinator

Other Required Skills:

• Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.
• Demonstrate strong cross-functional collaboration s

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