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ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.
Clinical Data Coordinator I
Location
India
Posted
54 days ago
Salary
0
Seniority
Mid Level
Job Description
Clinical Data Coordinator I
ICON plc
Clinical Data Coordinator I ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development As a CDC I at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency. Key responsibilities include: - Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures. - Review clinical and third-party data based on edit specifications and data review plans. - Issue clear, accurate, and concise queries to investigational sites. - As required, communicate effectively with peers, clinical data scientist and functional management. - Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.). Your Profile: You will bring relevant clinical research experience, along with the following qualifications and skills. Required qualifications and experience: - Bachelor's degree in a relevant field, such as Life Sciences or Healthcare. - Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry. - Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar). - Strong attention to detail and the ability to work effectively in a fast-paced environment. - Excellent communication skills and the ability to collaborate with cross-functional teams. - Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply
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Oncology Data Specialist
UT Southwestern Medical CenterWith over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals.
Role Description Oncology Data Specialist - Position: Full-Time, 100% Remote - Applicants are required to reside in Texas - Work Schedule: Monday-Friday from 7:00am - 3:30pm Job Duties: - Abstracting: Identify analytic & nonanalytic cases within 6 months of diagnosis and collect data as outlined in the FORDS manual, current State Cancer Registry Handbook, and any information required by Cancer Committee Members. Abstract a minimum of 6 abstracts per day (1 abst/1.15 hr). Minimum of 35 cases completed per week for remote abstractors. - Maintain a 95% accuracy rate in abstracting, suspensing, and casefinding as required by the Cancer Committee Performance Improvement Plan. - Follow-up: Identify information necessary for a completed "follow-up." Maintain follow-up according to ACoS Standards. Demonstrate/obtain follow-up information via telephone calls, internet, Oacis, and Siemens to assist in follow-up. Perform data entry of information obtained in the follow-up process. - Staging Forms: Identify cases eligible for staging. Place the proper staging form in the medical record. Identify the physician responsible for completing the staging form. - Prepare charts for physician review. Assist physicians during QA review. - Peer Review: Review other registrar's abstracts. Give and receive constructive criticism. - Attend at least one state, local, regional, or national meeting annually to be in compliance with ACOS. Qualifications - College level courses in Medical Terminology, Anatomy and Physiology or Associate's Degree or equivalent in experience. - Oncology Data Specialist Certification Upon Hire. Requirements - Previous experience in an approved (Cancer Program) tumor registry (preferred). Benefits - PPO medical plan, available day one at no cost for full-time employee-only coverage. - 100% coverage for preventive healthcare - no copay. - Paid Time Off, available day one. - Retirement Programs through the Teacher Retirement System of Texas (TRS). - Paid Parental Leave Benefit. - Wellness programs. - Tuition Reimbursement. - Public Service Loan Forgiveness (PSLF) Qualified Employer. Company Description With over 75 years of excellence in Dallas-Fort Worth, Texas, UT Southwestern is committed to excellence, innovation, teamwork, and compassion. As a world-renowned medical and research center, we strive to provide the best possible care, resources, and benefits for our valued employees. Ranked as the number 1 hospital in Dallas-Fort Worth according to U.S. News & World Report, we invest in you with opportunities for career growth and development to align with your future goals. Our highly competitive benefits package offers healthcare, PTO and paid holidays, on-site childcare, wage, merit increases and so much more.
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