Scientific Project Coordinator

🔥 14 hours ago

🎸 Tennessee – Remote

🎸 Tennessee – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 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

• Provide operational oversight and support for outsourced analytical testing in ADA and PK bioanalysis • Monitor timelines and scheduling of bioanalytical testing to align with data transfer deliverables • Manage analytical method support documentation, including dosing documents, reagent qualifications, expiry extensions, and bioanalytical reports • Monitor outsourced bioanalytical method performance and identify analytical trends • Communicate project updates and issues to scientific project managers, internal scientists, CRO staff, and operational teams • Manage and lead recurring cross-functional meetings • Facilitate contracts with external suppliers • Support shipping and reagent requests • Maintain issue and program-specific tracking logs • Support sample disposition requests • Maintain external collaboration sites • Manage logistics for new clinical study initiation • Participate in or lead operational process improvements • Participate in all aspects of study life cycle from initiation to closure

🎯 Requirements

• B.S. in Life Sciences or related field • Master's degree and/or associate’s degree may be considered with different levels of work experience • 4 years of industry-relevant project and/or laboratory management experience required • 1–3 years of Large Molecule PK/ADA/NAb Bioanalytical bench experience preferred • Validation experience in the laboratory is a plus • Experience working with vendors/service providers preferred • Ability to work Monday–Friday, Pacific Coast Hours, with occasional meetings later in the day • Demonstrated project and timeline management skills • Solid organizational skills with attention to detail and ability to develop and follow processes • Strong oral and written communication skills, including team collaboration and technical writing • Understanding of clinical trial processes • Working knowledge of GLP, GCP and/or CLIA • Strong computer literacy, including word processing, SharePoint, presentation, and spreadsheet applications • Ability to work effectively in a cross-functional team matrix environment • Ability to read, analyze, and interpret business periodicals, professional journals, technical procedures, and governmental regulations • Ability to write reports, business correspondence, and procedure manuals

🏖️ Benefits

• Fully remote work arrangement

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