Associate Data Manager

🔥 12 hours ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

📊 Data Scientist

🚫👨‍🎓 No degree required

👻 Ghost score 10%

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LabConnect

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2002

🏥 Healthcare

💊 Pharmaceuticals

🧬 Biotechnology

💰 $24.5M Series A - LabConnect on 2017-06

Healthcare • Pharmaceuticals • Biotechnology

LabConnect is a global central laboratory solutions partner that provides technology-driven, customized, orchestrated, and scalable laboratory and data services to support clinical trials and drug development worldwide. Its offerings include central and specialty bioanalytical testing, radiopharmaceutical support, decentralized/near-home collection, custom collection kits and high-volume kitting, companion diagnostics and assay validation, data management and harmonization, regulatory and scientific project management, and commercial/post-market support. LabConnect serves sponsors and CROs across multiple therapeutic areas (oncology, vaccines, cell and gene therapy/ATMPs and more), emphasizing program oversight and operational execution for clinical research.

📋 Description

• Reconcile regulated laboratory data streams for clients • Remediate omissions, inconsistencies, and inaccuracies in client data streams • Review laboratory data files against data transfer specifications • Create test laboratory data for test transfer files • Create low-complexity study laboratory data transfer specifications and communicate amendments to clients • Suggest and contribute improved real-time validity checks in the LabConnect central laboratory information management system • Maintain data transfer specifications as directed by the study Data Manager • Formulate systems and ensure projects meet strategic needs • Initiate and deliver scheduled or requested data transfers to clients or designated recipients • Verify data transmissions comply with file structure, format, layout, and transfer specifications • Ensure consistency of analyte reference ranges, decimal precision, units of measure, and correlation factors • Formulate, install, and verify laboratory unit conversion tables • Respond to client queries about clinical data streams and document outcomes in client databases • Coordinate with internal teams and Investigator Support Services to resolve queries and remediate errors • Maintain study schedules according to contracted agreements and client communications • Perform routine work under the direction of the group manager

🎯 Requirements

• Associate’s degree or university program certificate in a biologic science concentration preferred • Four to six years of experience in the clinical trial industry strongly preferred • An equivalent combination of above education and experience will be considered • Laboratory experience preferred • Experience in clinical trial protocol development and FDA 21CRF11/GCP strongly preferred • Certification as an ASCP Medical Technologist or Medical Laboratory Technician preferred • Excellent attention to detail • Ability to adhere to established timelines, processes and procedures • Strong planning and problem-solving skills • Ability to work independently and collaboratively • Organization, time management, communication, multitasking, interpersonal and listening skills • Ability to adapt to changing environments and requirements • Verbal comprehension and ability to translate client needs to team members • Ability to make quick, well-thought-out decisions • Customer service/client relationship management skills • Prolonged periods of sitting at a desk and working on a computer • Ability to communicate effectively via phone, video, and email • Ability to use hands and fingers to operate a computer and other office equipment

🏖️ Benefits

• Equal Opportunity Employer committed to diversity and an inclusive workplace • Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job • Minimal travel requirement