Clinical Data Specialist

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    "datePosted": "2026-05-11",
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      "state": "Illinois",
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    "description": "<p><span style=\"font-weight: bold\">Shape the Future of Cancer Treatment at Luminate Medical </span></p>\n<p>At Luminate, our mission is to make cancer care more human.  </p>\n<p>Our first two products, <span style=\"font-weight: bold\">Lily </span>and<span style=\"font-weight: bold\"> Lilac</span>, are revolutionary wearable devices designed to address hair loss <br>and peripheral neuropathy respectively - two of the most common and difficult side effects of cancer <br>treatment. We have an exciting pipeline focused on building products that help cancer patients to live, not <br>just survive. <span style=\"font-weight: bold\">Lotus</span>, our latest solution is a next-generation system designed to make at-home cancer care <br>more accessible and efficient for both patients and clinics. </p>\n<p><br>We’re looking for a <span style=\"font-weight: bold\">Clinical Data Specialist</span> to own and drive clinical data activities across our clinical <br>trials, from EDC build through to data cleaning and database readiness. This is an exciting opportunity <br>to be part of a multi-award-winning team and play a decisive part in the development and production <br>of life changing devices. Above all, you will need to enjoy working in a fast-paced environment, be <br>passionate about working with people, and thrive in taking responsibility for delivering projects on<br>time to make a real-world patient impact.  </p>\n<p><br><span style=\"font-weight: bold\">Working at Luminate Medical </span><br>• This is a key early hire at a rapidly growing company. You will have an opportunity to shape the <br>development of multiple high-impact patient-facing products and gain first-hand insights into the <br>growth of a start-up. <br>• We offer a highly competitive salary comparable with multinational medical device companies, a <br>flexible benefits package (including health insurance and pension), alongside a company laptop, <br>headphones and camera. <br>• We believe in quality of life in our products and for our people, and offer flexible working hours, <br>and a generous vacation policy. <br></p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">What You Will Do: </span><br>• Manage clinical data activities across one or more clinical trials <br>• Generate and manage data queries with the EDC and work directly with clinical sites to resolve <br>queries in a timely manner <br>• Develop and pull study reports (e.g., data listings, query reports, data completeness metrics) <br>• Ensure data integrity and quality through ongoing data reviews, cleaning, and reconciliation <br>activities <br>• Support database lock activities and ensure audit readiness <br>• Build, configure, and maintain EDC systems (including CRF design, edit checks, and data <br>structure, medical coding) <br>• Lead User Acceptance Testing (UAT), including test script development and execution <br>• Contribute to development of data management plans, data review guidelines, and SOPs <br>• Identify opportunities to improve data workflows and implement scalable processes in a startup <br>environment </p>\n<p><br><span style=\"font-weight: bold\">Personal Attributes – The Ideal Candidate Is: </span><br>• Creative: A creative problem solver who is enthusiastic about new ideas.  <br>• Open: A proactive team player who seeks to help develop your teammates. You are willing to <br>adopt, engage with and shape company culture in a positive manner. You can give and receive <br>candid feedback in a constructive and positive manner.  <br>• Communicative: Proficient in written and verbal communication and collaboration skills. You are <br>able to share ideas and support exploration of other ideas.   <br>• Self-Driven: You have a sense of urgency in your work and thrive when taking responsibility for <br>tasks.  <br>• Organised: You can prioritise your list of tasks with input from more senior colleagues and <br>ensure actions are completed on time. </p>\n<p><br><span style=\"font-weight: bold\">Experience Requirements – The Ideal Candidate Must Have: </span><br>Qualification: Bachelor’s degree in Life Sciences, Clinical Research, Data Science, or related field <br>Experience: 3–7+ years with a Bachelor’s Degree, or 0-3+ years of experience with a Master’s Degree <br>Technical Skills:  <br>• Experience or coursework related to clinical trial data capture <br>• Hands-on experience with EDC systems (e.g., Clincapture Captivate, Medidata Rave, etc.)  <br>• Experience building EDCs (CRFs, edit checks, database structure)  <br>• Experience performing UAT  <br>• Understanding of data cleaning, query management, and database lock processes <br>Communication Skills:  <br>• Experience working directly with clinical research sites to resolve queries  <br>• Ability to clearly communicate data issues and drive resolution across stakeholders <br></p>\n<p><br></p>\n<p><span style=\"font-weight: bold\">Experience Advantages – It Would Be Advantageous to Have: </span><br>• Experience in medical device clinical trials (especially NSR or pivotal studies) <br>• Experience in startup, small teams, and/or fast-paced environments <br>• Experience supporting regulatory submissions (e.g., FDA) <br>• Experience supporting data analysis and collaborating with biostatisticians  <br>• Experience working on blinded studies or complex trial designs <br>• Exposure to oncology trials and working with oncology research sites </p>\n<p><br><span style=\"font-weight: bold\">Don’t have all of these requirements? </span><br>Some people are less likely to apply for a role unless they are 100% qualified. Your experience, skills <br>and passion will set you apart – tell us what you have learned and achieved, whether personal or work<br>related! With the right mindset, many of the skills above can be learned on the job. If this role excites <br>you, don’t let the description hold you back!</p>",
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