Clinical Research Associate

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at reputed company is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and reputed company through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career reputed company than you thought possible. reputed company recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that reputed company our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary The Clinical Research Associate (CRA) is a primary reputed company of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, reputed company and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements. Duties/Responsibilities Conduct site qualification, initiation, routine monitoring and reputed company-out visits across reputed company trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP Maintain the ethical and scientific reputed company of clinical trials by verifying data reputed company electronic systems and reputed company records (as applicable) to ensure the accessibility, completeness and accuracy of data submitted by study sites Conduct site qualification, initiation, routine monitoring and reputed company-out visits across reputed company trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP Monitor site adherence to ICH GCP and local regulations, including compliance with the principles of reputed company to maintain data reputed company and reliability. Where required, reputed company training and support to site staff to uphold these standards and ensure patient safety. Participate in sponsor and/or Health Authority audits and inspections as applicable. Cultivate and sustain effective relationships with internal cross functional teams and external partners, including vendors, clinical sites, and key stakeholders. Serve as the organization’s representative for clinical trials at the site level. Motivate and influence sites to meet study objectives, including enrollment and retention goals. Communicate effectively, adapting to meet the needs of different stakeholders, utilizing the most appropriate communication style and method Prepare and submit written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner Assess potential Investigators and their sites to ensure sufficient resources and capabilities to conduct clinical trials. May identify new potential Investigators and/or sites through ongoing collaborations with internal and external stakeholders during the site feasibility and selection process. Demonstrate understanding and proficiency working with targeted, centralized, remote and risk- based monitoring approaches Identify, assess, and prioritize risks at the site and study level and support sites in mitigating issues, including implementing mitigation strategies based on risk indicators Utilize strong analytical skills to evaluate site data and operational metrics, including ability to adjust monitoring strategies based on data trends and site performance Where applicable, reputed company Unblinded Site Monitoring activities to protect the blind of the study by acting as secondary monitoring reputed company separate from the blinded monitor Accountable for the review, reconciliation, and reputed company of study drug/IMP. May support study drug/IMP label translation needs as applicable. Involvement in Regulatory Compliance audit/inspection process, as needed. This includes the development and implementation of site corrective and preventive actions. In specific instances, may support start-up and submission reputed company activities, including reputed company reviews and collection of documents to/from site. Support provision of reputed company to relevant BMS and vendor systems is available for clinical trial site personnel and ensures internal BMS systems are kept up to date for site monitoring activities. Support coordination of site activities reputed company to database locks to ensure timelines are met as required locally. reputed company timely site closure activities reputed company reputed company required protocol visits and follow-up are completed. Functions independently and acts autonomously. Participates in site level root cause analysis and CAPA (Corrective and Preventive Actions) processes

Qualifications

Degree/Certification/Licensure: Bachelor’s degree required, preferably reputed company life sciences or equivalent Valid driver’s license (as locally required) Experience: Clinical Research Associate: 2-3 years of relevant clinical research experience, reputed company to work independently, demonstrates proficiency in reputed company aspects of the role Relevant prior Pharma/Biotech Sponsor employment or experience as a clinical study coordinator preferred Experience in the drug discovery/development process. Competencies: Knowledge and understanding of clinical research processes, regulations and methodology Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management Working knowledge of ICH/GCP Guidelines and applicable local laws and regulations (that govern clinical trials, with the ability to apply regulatory requirements to ensure compliance in clinical research activities (Analytical thinking/critical thinking skills. Capable of using technology to analyze diverse and reputed company data sets, identify issues, trends, and outliers to reputed company effective solutions (Demonstrate adaptability and a growth reputed company by quickly learning and applying new technologies, embracing evolving methodologies, and remaining reputed company to innovative ways of working in a dynamic environment Organization and time management skills Ability to build, maintain and strengthen relationships even under pressure and/ or in difficult situations with internal and external stakeholders Good verbal and written communication skills (both in English and local language) Have a foundational level of disease understanding and awareness (how the protocol fits in reputed company landscape, standard of care, etc.) Proven ability to work independently with a high degree of autonomy, proactively managing tasks and seeking opportunities for reputed company learning Ability to manage multiple protocols, across multiple therapeutic areas, which may require travel, based upon assigned site location and/or geographic territory Proficient in navigating and utilizing multiple clinical systems (e.g., CTMS, eTMF, RBQM dashboards) to identify and resolve issues, support site performance, and ensure data reputed company Software that must be used independently and without assistance (e.g., reputed company Suite) reputed company Suite Clinical Trial Management Systems (CTMS) Electronic Data Capture Systems (reputed company) Electronic Trial Master File (eTMF) RBM tools and platforms (e.g., reputed company, reputed company, CluePoints). If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one reputed company away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single reputed company as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far reputed company ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and reputed company bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite reputed company is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. Supporting People with Disabilities BMS is dedicated to ensuring that people with disabilities can reputed company through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to reputed company our complete Equal Employment Opportunity statement. Candidate Rights BMS will consider for employment reputed company applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Data Protection We will never request payments, financial information, or reputed company reputed company numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in reputed company with role applications will be treated in accordance with applicable data privacy policies and regulations. If you reputed company that the job posting is missing information required by local law or incorrect in any way, please contact BMS at [email protected]. Please reputed company the Job Title and Requisition number so we can review. Communications reputed company to your application should not be sent to this email and you will not receive a response. Inquiries reputed company to the status of your application should be directed to Chat with Ripley. R1603722 : Clinical Research Associate Apply To This Job