Associate Director, Clinical Assay Strategy, Flu
$179k - $212kCSL
CSL Seqirus is a global leader in influenza prevention and the world’s second-largest influenza vaccine provider, operating as a specialized division of CSL Limited. Headquartered in Melbourne, Australia, with major manufacturing hubs in Holly Springs, NC, and Liverpool, UK, the company operates the world’s largest cell-based vaccine facility and serves as a primary partner to governments for global pandemic preparedness. Joining Seqirus now means being part of an agile team committed to developing vaccines that make a meaningful difference worldwide. Could you be our next Associate Director, Clinical Assay Strategy-Flu? The job is in our Waltham, MA Office. This is a hybrid position and is onsite three days a week. You will report to the Director, Clinical Assay Strategy. This role is intended for a recognized subject matter expert who understands the scientific, operational, and regulatory evolution of influenza immunogenicity assessment, including HAI, microneutralization (MN), ELLA, and multiplex platforms, and can strategically navigate assay modernization while maintaining regulatory alignment. You will provide scientific leadership and external oversight of vaccine serology and biomarker assays supporting clinical development programs. This is a strategic, non-laboratory-based role responsible for assay design, validation oversight, regulatory alignment, and vendor governance across global clinical programs. Influenza Immunology & Assay Strategy Develop and execute clinical assay strategies for influenza vaccine programs across all phases of clinical development. Provide expert guidance on HAI assay design, optimization, regulatory expectations, and historical correlates of protection. Lead strategic implementation and interpretation of microneutralization (MN) assays. Oversee ELLA, Luminex-based total IgG, subclass, and Fc-effector analyses. Evaluate and guide adoption of multiplex platforms (e.g., Luminex) for expanded immune profiling. Lead assay bridging and concordance strategies during platform evolution or vendor transition. Assess context-of-use and regulatory acceptability of modernized assay platforms. Clinical Bioanalytical Validation & Regulatory Readiness Oversee assay qualification, validation, transfer, and lifecycle management aligned with FDA, EMA, ICH, and WHO guidance. Ensure validation parameters are appropriate for intended clinical endpoints (precision, accuracy, specificity, robustness). Provide strategic input for label-enabling immunogenicity studies. Support regulatory submissions with validation documentation and responses to health authority queries. Anticipate regulatory risks associated with assay modernization in influenza programs. Externalization & Vendor Oversight Lead technical evaluation and selection of external bioanalytical laboratories. Oversee assay transfers ensuring concordance, compliance, and data integrity. Establish vendor governance frameworks, KPIs, and performance oversight. Manage complex troubleshooting and scientific escalations with external partners. Ensure operational excellence across high-throughput influenza clinical serology programs. Cross-Functional Collaboration Partner closely with Research, Clinical Development, Regulatory Affairs, Statistics, and CMC teams. Translate immunological data into strategic development decisions. Provide scientific leadership in a matrixed environment. Represent the organization at scientific conferences and regulatory forums. Qualifications & Experience Bachelor's in Life Science. PhD preferred in Immunology, Virology, Microbiology, or related Life Sciences discipline preferred. 4+ years of industry experience in vaccine development. Experience in influenza vaccine required Demonstrated expertise in HAI and MN assay validation and regulatory positioning. Experience in ELISA and multiplex immune assay development. Experience supporting regulatory submissions involving vaccine immunogenicity endpoints. Proven experience managing outsourced clinical bioanalytical programs. The expected base salary range for this position at hiring is $179,000 - $212,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity. #J-18808-Ljbffr
$179k - $212k
...team committed to developing vaccines that make a meaningful difference worldwide. Could you be our next Associate Director, Clinical Assay Strategy-Flu? The job is in our Waltham, MA Office. This is a hybrid position and is onsite three days a week. You will report...SuggestedWork at officeWorldwide3 days per week- ...leader in influenza prevention and the world’s second‑largest influenza vaccine provider. This role is the Associate Director for Clinical Assay Strategy – Flu, based in Waltham, MA, and is hybrid (onsite three days a week) reporting to the Director of Clinical Assay...Suggested3 days per week
$171k - $236k
...Job Description Role Summary The Associate Director Clinical Scientist contributes to the execution of the clinical development plan for the candidate... ...one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long‑term...Suggested$176.1k - $287.3k
...projects across diverse therapeutic areas. As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy, development, and lifecycle management of... ...IVD partners to deliver fit-for-purpose assays that meet global regulatory requirements and...Suggested- ...effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial goals and regulatory... ...at regulatory meetings. Qualifications Associate Director, Clinical Pharmacology PhD with typically 4+ years...Suggested
$174k - $212k
...Associate Director, Clinical Data Management Watertown, MA Company Overview Prime Medicine is a leading biotechnology company dedicated to creating... ...of Clinical Data Management to lead clinical data strategy and execution across gene editing programs from first‑in‑human...$161.7k - $202.2k
...Position Summary The Associate Director, Clinical Scientist is a highly collaborative, execution-focused role that supports the development, evaluation... ...Affairs, and Regulatory Affairs to translate clinical strategy into operational deliverables and ensure rigorous ongoing...$177.7k - $240.3k
...Overview The Associate Director (AD), Clinical Science will be a member of the global clinical development team, working closely with other members... ...to support investigations that deliver the development strategies for therapeutic compound(s) under development. Under supervision...Flexible hours$175k - $226k
...About eGenesis eGenesis is a clinical-stage biotechnology company developing human-compatible... ...headquartered in Cambridge, MA. The Associate Director, Clinical Science is responsible for... ...and execution of clinical development strategies, support regulatory submissions, and...- ...Clinical Pharmacology Lead Exciting opportunity in Clinical Pharmacology! Our Clinical... ...Pharmacology Team is looking for an Associate Director to support the exciting portfolio in... ...and diseases for rational development strategies and decisions, as well as optimal study...Relocation package2 days per week
- ...Associate Director/ Director, Clinical Pharmacology | Commercial Biotech Full Relocation Support Offered (if relocating from outside MA) APX Life Sciences... ...'ll play a key role in shaping Clinical Pharmacology strategy across multiple development programmes. Working within...RelocationRelocation package3 days per week
$139.1k - $231.9k
Role Summary Exciting opportunity in Clinical Pharmacology! Our Clinical Pharmacology Team is looking for an Associate Director to support the exciting portfolio in Internal Medicine... ...and diseases for rational development strategies and decisions, as well as optimal study...Permanent employmentH1bLocal areaVisa sponsorshipWork visaRelocation package2 days per week$139.1k - $231.9k
Associate Director, Clinical Pharmacology United States - Massachusetts - Cambridge United States - Connecticut - Groton United States - Pennsylvania... ...PK/PD analyses, PK/immunogenicity/biomarker measurement strategies, etc.). Plan and oversee study level activities...Permanent employmentH1bVisa sponsorshipWork visaRelocation package2 days per week$174k - $196k
Associate Director, Clinical Pharmacology Cambridge, Massachusetts, United States City Therapeutics is advancing a next-generation platform for... ...Translational Sciences Team to help shape the clinical development strategy of our growing portfolio. The Associate Director of...Work at officeWork from homeFlexible hours- ...CONTRACT ROLE – Associate Director, Clinical Biomarkers Watertown, MA – CONTRACT POSITION What’s the opportunity... ...implementing our clinical biomarker strategy across one or more clinical programs.... ...concrete plan for sample collection, assay execution, timelines, and...Permanent employmentContract work
$150.98k - $251.63k
...advance your career? If so, this Associate Director – Diagnostics Oncology... ...implementation of GSK diagnostic strategies supporting drug development, including technical, clinical, regulatory, commercial,... ...implementation of diagnostic assays within a clinical trial. Collaborate...Odd jobLocal areaRemote work$101k - $151.5k
## Associate Director, Clinical ServicesApplylocations: Wellesley Hills, Massachusetts: Hartford, Connecticut: Kansas City, Missouri: Milwaukee,... ...management activities that advance Sun Life’s health capabilities strategy, improve broker and client engagement, and support...Work at officeLocal areaFlexible hours2 days per week- ...Job Summary The Associate Director of Clinical Data Management is a critical position within the ModeX clinical operations team. This position is responsible for successfully leading the execution of all data management activities, ensuring focus on data integrity, validity...
- ## Associate Director, Clinical ScientistApplyremote type: Site Basedlocations: South Boston, MAtime type: Full timeposted on: Posted 11 Days Agojob... ...and competitive intelligence to support study and program strategy* Develop scientific and protocol training presentations to...Remote work
$120k - $160k
...of research locations, mobile clinics, and clinicians across the globe... ...Reporting to the Sr. Director of Study Feasibility & Clinical Partnerships, the Associate Director and Director of Study... ...shaping and advancing feasibility strategy, ensuring robust site evaluation...Full timeTemporary workWork at officeLocal areaRemote workWorldwideVisa sponsorshipWork visaFlexible hours- ...Associate Director, Clinical Scientist CRISPR Therapeutics is searching for an Associate Director, Clinical Scientist to provide scientific input... ...and competitive intelligence to support study and program strategy Develop scientific and protocol training presentations...Remote work
$180k - $210k
...Employment / Unlimited Job Requisition ID: 11932 Role Associate Director, US Corporate Strategy About Servier Servier in the U.S. is a Boston-based, commercial... ...to ensure strategies are grounded in scientific, clinical, and commercial realities Lead discrete workstreams by...Full timeContract workTemporary workWork experience placementFlexible hours$95k - $135k
...different stages of maturity. Some are the industry standard, some are starting off. There is a lot to learn, there is room to grow. Our Strategy function is responsible for the success of our products in the market; that’s from guiding the product to client success. Today,...Work experience placementLocal areaFlexible hours- ...60 and others. If you're as passionate about your future as we are, join our team. KPMG is currently seeking an Associate Director, Corporate Strategy to join our Corporate Strategy organization. Responsibilities: Support first-principles thinking to define firm...H1bLocal areaShift work
- ...Job Description Job Description Job Title: Associate Director Clinical Operations Location: Waltham, Massachusetts Type: Perm Work Model: Hybrid – 2 days onsite in Waltham Leading Pharmaceutical Company located in MA is hiring a Associate Director Clinical Operations...Permanent employmentLocal area
- ...strategic and operational management of complex clinical supply activities across all phases of... ...bring deep expertise in supply chain strategy and vendor oversight, with a strong... ...Quality Assurance & Regulatory on activities associated with labelling, packaging,...Flexible hours
$154.4k - $242.55k
...Job Description Join Takeda as an Associate Director, Patient Access Brand Strategy & Operations – Dermatology out of our Cambridge, MA office. The Associate Director, Patient Access Brand Strategy & Operations – Dermatology is responsible for translating Dermatology brand...Minimum wageFull timeTemporary workWork at officeLocal areaRemote work- ...An Associate Medical Director (MD) performs the following roles: The Associate Medical Director will have administrative and clinical oversight of the program (alongside and assisting the Medical Director) to provide the highest quality of care utilizing state-of-the...
$143.6k - $215.4k
...EMD Serono, Inc. is seeking an Associate Director of US Medical Communications for Rare Tumors. This role involves leading communication strategies to convey scientific information effectively to healthcare professionals, ensuring alignment with patient care goals. The...$142.5k - $256.5k
...The Role Associate Director, Clinical Supplies Project Management is responsible for oversight and leadership of clinical supply activities for... ...clinical study. The scope includes the operational planning and strategy required to execute end-to-end supply management,...Permanent employment
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