Lead Clinical Data Manager

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    "ShortDescriptionStr": "Responsible for Clinical Data Management oversight for CooperVision sponsored clinical trials.  Oversees the entire lifecycle of clinical trial data from setting up the database, data collection, and data dissemination for analysis and reporting, ensuring data quality, integrity, and compliance of databases, while adhering to strict regulatory and international standards under Good Clinical Practice to ensure patients’ safety and play a crucial part in Helping People Experience Life’s Beautiful Moments.",
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    "ExternalDescriptionStr": "<p>At CooperVision, a division of CooperCompanies, we’re driven by a unifying purpose to help people to experience life’s beautiful moments. We are connected through our shared values - dedicated, innovative, friendly, partners, and do the right thing. As a leading global manufacturer of contact lenses, we are committed to helping improve the way people see each day. Through our diverse lens portfolio, we tackle the toughest vision challenges – including astigmatism, presbyopia, and childhood myopia. We offer the most complete collection of spherical, toric, and multifocal products available, enabling us to fit 99% of all contact wearers. Learn more at www.coopervision.com.</p><p>&nbsp;</p><p><strong>Job Summary:</strong></p><p>Leads all aspects of clinical data management activities from study initiation through database lock and study closeout. Develops, optimizes and controls data management system, including external clinical research centers in compliance with medical device regulations. Oversees and ensure that all CooperVision sponsored clinical trial data are accurate, complete, and compliant.</p><ul style=\"list-style-type: disc;\"><li><i>This role is not eligible for employer-sponsored work authorization now or in the future. Applicants must be authorized to work in the United States on a permanent and ongoing basis without the need for future sponsorship (i.e., H1B, STEM OPT extensions, TN, etc.)</i></li><li><i>This position requires full-time onsite work (5 days per week) in our San Ramon, CA. office and is not eligible for relocation assistance.</i></li></ul><p>&nbsp;</p>",
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    "ExternalPostedStartDate": "2026-05-28T21:08:44+00:00",
    "ExternalQualificationsStr": "<p><span lang=\"EN-GB\"><strong>Knowledge, Skills and Abilities:</strong></span></p><ul style=\"list-style-type: disc;\"><li><span lang=\"EN-GB\">Bachelor’s degree in life science, computer science or closely related discipline plus minimum of 8 years of experience in Clinical Data Management, or&nbsp;</span></li><li><span lang=\"EN-GB\">Master of Science in life science, computer science or closely related discipline plus minimum of 5 years of experience in Clinical Data Management&nbsp;</span></li><li><span lang=\"EN-GB\">Highly dependable, good time management and multitasking skillsets</span></li><li><span lang=\"EN-GB\">Proficiency with common electronic data capture (EDC) and clinical data management platforms, and clinical data systems (e.g., REDCap, Medrio, Medidata RAVE, Veeva).</span></li><li><span lang=\"EN-GB\">Expertise in database design, validation, and oversight of external data integration.</span></li><li><span lang=\"EN-GB\">Expert in the use of SQL to query datasets.</span></li><li><span lang=\"EN-GB\">Passion for exploring and adopting emerging technologies, including AI-enabled tools, to support innovation, operational excellence, and business transformation</span></li><li><span lang=\"EN-GB\">Strong problem-solving ability to navigate complex unforeseen situations</span></li><li><span lang=\"EN-GB\">Strong leadership skillsets to guide and mentor within and cross-functional team members</span></li><li><span lang=\"EN-GB\">Strong on written and verbal communications</span></li><li><span lang=\"EN-GB\">Experience with integrating data from external vendors or systems.</span></li><li><span lang=\"EN-GB\">Familiarity with statistical or visualization tools such as SAS or R is preferred.</span></li><li><span lang=\"EN-GB\">Ability to read and understand highly technical material.</span></li></ul><p>&nbsp;</p><p><span lang=\"EN-GB\"><strong>Work Environment:</strong></span></p><ul style=\"list-style-type: disc;\"><li><span lang=\"EN-GB\">On-site 5 days a week in-office required&nbsp;</span></li><li><span lang=\"EN-GB\">Normal office environment and ophthalmic clinical exam room&nbsp;</span></li><li><span lang=\"EN-GB\">Sedentary to light physical effort necessary to perform the job.&nbsp;</span></li><li><span lang=\"EN-GB\">Extensive contact with employees and external researchers</span></li><li><span lang=\"EN-GB\">Extensive computer and keyboarding</span></li></ul><p>&nbsp;</p><p>For U.S. locations that require disclosure of compensation, the starting base pay for this role is between $164,819.00 and $219,758.00. per year and may include cost of living adjustments. &nbsp;The actual base pay includes many factors and is subject to change and modification in the future. &nbsp;This position may also be eligible for other types of compensation and benefits.<br><br>We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender, gender identity or expression, or veteran status. We are proud to be an equal opportunity workplace.</p><p><strong>#LI-SD1</strong></p>",
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