Clinical Data Manager

🕒 Yesterday

🌽 Illinois – Remote

🌽 Illinois – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Tempus AI

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2015

🏥 Healthcare

🧬 Biotechnology

🤖 Artificial Intelligence

Healthcare • Biotechnology • Artificial Intelligence

Tempus AI is an advanced healthcare technology company that specializes in precision medicine through the use of AI and genomic profiling. The company provides innovative solutions across various medical fields, including oncology, cardiology, neurology, and psychiatry. Tempus enables healthcare providers to make informed treatment decisions by integrating real-world data, clinical trial matching, and algorithmic testing to improve patient outcomes and accelerate drug development.

📋 Description

• Contribute to data management activities supporting clinical studies across all stages of clinical drug development • Lead cross-functional reviews of eCRF content and support eCRF development • Support database build activities, including review of edit check specifications and user acceptance testing • Monitor vendor data collection, coding, and cleaning through study metrics and targeted data reviews • Oversee database lock activities and archive study data • Collaborate with Biostatistics, Statistical Programming, Clinical Operations, Medical, Quality Assurance, Drug Safety and Pharmacovigilance, CROs, laboratories, and other vendors • Establish cross-functional internal data review plans, coordinate data cuts/transfers, and conduct data reviews • Review CRO data management plans, CRF completion guidelines, edit check specifications, external data transfer specifications, and other study documentation • Represent data management and communicate requirements, strategy, timelines, and deliverables in internal and external meetings • Participate in drafting and/or reviewing timelines and ensure deliverables and milestones are met • Review clinical protocols/amendments, clinical study reports, statistical analysis plans, and related documents • Support GCP inspection readiness • Demonstrate alignment with company values • Perform other duties as assigned

🎯 Requirements

• BS/BA in scientific discipline required; MS or equivalent preferred • At least 8 years related experience in a CRO/pharmaceutical/biologics/biotechnology company • Study/Vendor oversight experience • Experience with global studies, utilizing an outsourced CRO model • Expert knowledge of Data Management processes, efficient design/build of an EDC data management system and other Clinical Trial/Data Management Systems • Knowledge and understanding of regulations and industry-adopted data standards, such as CDISC SDTM and CDASH • Experience working with EDC data management systems • Understanding of ICH GCP as well as general knowledge of industry practices and standards • Knowledge and understanding of regulatory requirements and expectations for clinical data systems including 21 CFR Part 11 • Highly motivated and flexible, with excellent organizational and time management skills • Ability to work independently and as part of a multi-disciplinary team • Proficient in Microsoft Word and Excel • Preferred: Experience working with Medidata Rave EDC • Preferred: Experience using standardized medical terminology, including MedDRA and WHODrug • Preferred: Prior experience working for both a Sponsor company and a CRO • Preferred: Early phase clinical trial experience • Excellent interpersonal and communications skills, verbal and written • Problem solving and organization skills • Proven ability to work independently • Self-motivated, pro-active, and resourceful • Strong ability to manage managers and/or individual contributors • Excellent analytical and problem-solving skills • Excellent communication skills with a diplomatic approach • Excellent ability to lead cross-functional initiatives related to Data Management • Demonstrated proactive thought process to minimize and mitigate risk independently • Demonstrated ability to conduct root cause analysis cross-functionally in business problem solving and process improvement development • Excellent presentation skills, internal and external

🏖️ Benefits

• Full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position • May involve travel