Senior Clinical Trials Specialist

Job not on LinkedIn

🔥 3 minutes ago

🇺🇸 United States – Remote

💵 $80.2k - $120.4k / year

⏰ Full Time

🟠 Senior

👻 Ghost score 0%

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Adaptive Biotechnologies Corp.

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2009

🏥 Healthcare

🧬 Biotechnology

⚕️ Healthcare Insurance

💰 $125M Post-IPO Debt on 2022-09

Healthcare • Biotechnology • Healthcare Insurance

Adaptive Biotechnologies Corp. is a leader in immune-driven medicine, aiming to revolutionize disease detection and treatment. By utilizing the adaptive immune system, the company develops diagnostic and therapeutic solutions powered by its innovative Immune Medicine platform. They offer clinical diagnostics, particularly in Minimal Residual Disease (MRD) testing, and engage in drug discovery and therapeutic development through adaptive immunosequencing technologies. Their biopharma services support the progression of clinical trials and the development of transformative medicines. Adaptive Biotechnologies leverages the complex biology of the immune system, decoding it to advance medical science and improve patient outcomes.

📋 Description

• Maintain detailed requirements of MRD-related trial protocols, facilitating sample processing and data generation • Support the Medical Science Liaison team in designing and managing clinical trial collaborations • Partner with Quality Assurance to document deviations and nonconformances in accordance with GCLP practices • Coordinate with internal and external stakeholders regarding dual workflow patient samples • Lead creation of customer-specific clinical trial collateral • Assist customers with patient linking requests, including re-accessioning or re-processing events • Provide Tier II support for customer issues and complaint resolution • Lead onboarding activities for new clinical trial customers • Serve as point of contact for trial investigators and staff regarding ordering, specimen type, sample processing, and reporting timeframes • Attend investigator and participating-site meetings and generate meeting/project documentation • Partner with Biological Sample Management and Lab Operations to ensure sample receipt, processing, and results delivery according to trial agreements and analytical plans • Act as subject matter expert on assigned clinical trial requirements • Collaborate with Biological Sample Management, Lab Operations, Accounts Receivable, Medical Affairs, and Quality Assurance • Streamline processes, improve efficiency, and enhance standard operating procedures • Contribute to business goal achievement • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree or an equivalent combination of education and experience • 2 to 4 years of prior Clinical Trials, Clinical Services or Client Services experience highly preferred • Experience working with GCLP trials or in an FDA regulated environment preferred • Strong customer and patient focus with a demonstrated understanding of HIPAA requirements • Familiarity with basic laboratory and customer service-related systems such as LIMS and SFDC • Strong attention to detail and meticulous data entry skills • Ability to manage multiple tasks to completion in a dynamic office setting • Effective and professional communication skills for engagement with both internal and external personnel • Excellent written communication skills, including technical proficiency with Word, Excel, PowerPoint, etc. • Flexible team-player with the ability to take on new assignments • Adaptive is not currently sponsoring candidates requiring work authorization support for this position

🏖️ Benefits

• Equity grant • Bonus eligible • Some travel may be required • Adaptive benefits program (benefits-at-a-glance referenced)