Manager, Biomarkers and Bioanalytical Operations

About   T his   R ole:   The Biomarker and Bioanalytical Operations Study Manager   leads   PK, ADA, and biomarker execution across clinical studies, partnering with study teams and CROs to deliver high-quality data on time. This role is critical to achieving key study endpoints and advancing programs through drug development and reports to   the Head of Biomarker and Bioanalytical Operations.    What   You’ll   Do   Serve as the primary Biomarker and Bioanalytical Operations lead for internal teams and external partners across Phase 1–4 studies   Lead end-to-end operational execution of biomarker and bioanalytical activities, including sample collection, processing, shipment, testing, storage, and data delivery   Implement clinical biomarker and bioanalytical strategies for early- and late-stage programs   Provide operational and sample management   expertise   to Study Management Teams (SMTs) and Biomarker Sub-Teams (BMSTs)   Ensure compliant, high-quality   bio marker and bioanalytical sample   collection aligned with protocols, ICFs, ethical standards, and regulations   Oversee CROs, central labs, and specialty vendors; manage performance, timelines, quality, contracts, and deliverables   Review and contribute operational input to protocols, CRFs, ICFs, proposals, budgets, study plans, and contracts   Develop study-specific   bio marker and bioanalytical sample   collection, handling, analysis, transport, and storage strategies   Partner cross-functionally (Clinical Biomarker, Clinical Pharmacology, Clinical Operations, Data Management, Business Operations   & Contracts Partner ) to enable efficient execution   of the study   Define data collection, transfer, and reconciliation requirements with data management, bioanalytical leads, and vendors   Identify   operational risks, implement mitigation plans, and support interim and final biomarker   and bioanalytical   reporting   Lead operational meetings, RFPs, vendor selection, and process improvement initiatives   Maintain biomarker operations systems and documentation; represent on cross-functional teams   Operate independently with general supervision; support investigator meetings and internal/external presentations as needed   Who You Are    You excel in fast-paced clinical development environments dedicated to advancing new therapies to patients. Your   expertise   in scientific operations, GCLP, and CRO management enables effective collaboration across internal teams and external laboratory partners.   Required Skills    Minimum Education & Experience   Advanced degree (PharmD or PhD) with 2+ years of relevant industry experience; MA or MS with 6+ years; or BA/BS or RN with 8+ years of comparable clinical, life sciences, or similar industry experience.   Good knowledge of phase I-I V   clinical study operations as it pertains to specialty testing (PK, ADA, Biomarkers)    Experience working with contracted central labs and biomarker/bioanalytical testing labs including sample management, data management, testing  requirements  and timelines    Experience reviewing clinical protocols ,   ICFs , SOW,   and contracts   Experience obtaining contracts and an understanding of Master Agreements and associated contracts    Experience working within GCP, GLP, & GCLP guidelines     Must be  very organized  and  have the ability to  manage multiple projects at a time     Preferred Skills   Demonstrated ownership of operational execution and accountability for outcomes   Proven ability to manage CROs and external vendors effectively   Solid understanding of clinical trial conduct and the drug development process   Strong cross-functional collaboration and stakeholder partnership skills   Clear, confident verbal and written communication   Proactive approach to   identifying   and managing operational risks   Strong organizational and prioritization skills   Continuous improvement mindset with a focus on   optimizing   processes and efficiency   This role involves minimal travel, typically under 10%.   Job Level: Management Additional Information The base compensation range for this role is: $122,000.00-$163,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.  In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being ; including, but not limited to: Medical, Dental, Vision, & Life insurances Fitness & Wellness programs including a fitness reimbursement  Short- and Long-Term Disability insurance A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31) Up to 12 company paid holidays + 3 paid days off for Personal Significance  80 hours of sick time per calendar year Paid Maternity and Parental Leave benefit  401(k) program participation with company matched contributions Employee stock purchase plan  Tuition reimbursement of up to $10,000 per calendar year  Employee Resource Groups participation Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expa