Bioanalytical Study Manager
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<p style="text-align:left"><b>Work Schedule</b></p>Standard (Mon-Fri)<p style="text-align:inherit"></p><p style="text-align:left"><b>Environmental Conditions</b></p>Office<p style="text-align:inherit"></p><p style="text-align:left"><b><u>Job Description</u></b></p><p style="text-align:inherit"></p><p>Join Us as a Bioanalytical Study Manager - Labs – Make an Impact at the Forefront of Innovation</p><p></p><p>This is a fully remote role supporting our customer’s site in Eastern and Central Time Zones. We welcome applicants from all locations within the US.</p><p>Must be legally authorized to work in the United States without sponsorship.</p><p>Must be able to pass a comprehensive background check, which includes a drug screening.</p><p></p><p>Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.</p><p>Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.</p><p></p><p><b>Summarized Purpose</b><br>Join our dynamic team and lead the charge in supporting our clients development pipeline from a bioanalytical perspective. You'll manage bioanalytical operations for pre-clinical studies and clinical trials, ensuring timely delivery of quality data by coordinating activities between multiple stakeholders.</p><p></p><p><b>Essential Functions:</b></p><ul><li><b>Vendor Management:</b> Support the team contracting with third-party lab service providers for assay development and validation. Collaborate with business operations, procurement, and clinical teams to ensure appropriate SOWs and contracts.</li><li><b>Study Coordination:</b> Manage critical reagent supply and sample analysis. Work closely with bioanalytical strategy leads, clinical trial teams, and lab service providers to finalize study documents and meet timelines.</li><li><b>Documentation & Data:</b> Provide input into clinical trial documents (e.g., eCRFs, ICFs, SOWs). Drive the delivery of data transfer specifications and ensure data accuracy.</li><li><b>Sample Logistics:</b> Track and reconcile sample testing, resolving any issues that arise.</li></ul><p><b><u>Education and Experience:</u></b><b><u> </u></b></p><ul><li><b>Education:</b> BA/BS in a scientific degree + 2 years’ experience in a Bioanalytical laboratory.</li><li><b>Experience:</b><ul><li>Experience of working in a regulated environment</li><li>Understanding of clinical trial design</li><li>Good project management background</li><li>Strong communication and collaboration skills</li><li>Strong large molecule immunoassay-based bioanalysis experience<ul><li>Ideally with translational or biomarker experience</li></ul></li><li>Experience performing PK/ADA assays is required</li><li>Experience with biomarker techniques and/or flow cytometry is highly preferred.</li><li>Flow Cytometry experience preferred</li></ul></li></ul><p><b><i>In <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">some cases, an</span> equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.</i></b></p><p></p><p><b><u>Knowledge, Skills, and Abilities: </u></b></p><ul><li>Strong organizational and analytical skills.</li><li>Excellent written/verbal communication.</li><li>Ability to work both independently and as part of a team.</li><li>Multicolor panel design</li><li>Compensation and gating strategy</li><li>Using instruments like BD FACSCanto, LSRFortessa, Cytek Aurora</li><li>Data analysis in FlowJo</li><li>PBMC handling and staining</li></ul><p><br>Working Environment:<br>Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working <span style="overflow-wrap: break-word; display: inline; text-decoration: inherit; hyphens: auto;">environment/requirements</span> for this role:<br><br>• Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.<br>• Occasional drives to site locations, occasional domestic travel.<br>• Exposure to biological fluids with potential exposure to infectious organisms.<br>• Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.<br>• Personal protective equipment required such as protective eyewear, garments and gloves.<br>• Exposure to fluctuating and/or extreme temperatures on rare occasions.<br><br>Why join us?<br>When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.<br><br>Apply today to help us deliver tomorrow’s breakthroughs.</p><p></p><p></p><p></p><p></p>