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
$193.8k - $240.38k
Associate Director / Director, Clinical Pharmacology About the Position The Associate Director / Director of Clinical... ...includes oversight of PK sample strategy, bioanalytical testing, and data... ...oversight for bioanalytical assay development, validation, and sample...Suggested$171k - $236k
...from Deciphera’s platform in clinical studies, QINLOCK® (ripretinib... ...for adult patients with TGCT associated with clinically relevant physical... ...Description The Associate Director Clinical Scientist... ...’s competitive total rewards strategy that also includes annual performance...SuggestedFull timeFlexible hours- ...Therapeutics in Cambridge, MA is seeking an Associate Director of FP&A to serve as the lead finance... ...G&A and program teams. You will own clinical trial budgeting, the annual operating... ...with Bayer expectations and company strategy. You will build advanced financial models...Suggested
$161.7k - $202.2k
Zenas is a clinical-stage global biopharmaceutical company committed to becoming a leader... ...diseases. Our core business strategy combines our experienced leadership team... ...TRUE Innovation!Position Summary:The Associate Director, Clinical Scientist is a highly collaborative...Suggested- ...Biosciences is seeking an experienced and highly motivated Associate Director, Clinical Operations to serve as a key operational leader across our... ...while also contributing to broader Clinical Operations strategy, portfolio planning, process improvement, and cross-functional...SuggestedTemporary workWork at officeLocal areaImmediate startRemote work
$120k - $135k
....Discover your purpose. Embrace innovation. Experience #LifeatRealChem.Job Summary:Real Chemistry is looking for an Associate Director, Medical Strategy tojoin our growing team!Our Associate Directors play a pivotal role in guiding the direction of projects and aligning...Work at officeLocal areaRemote work2 days per week- ...effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial goals and regulatory... ...be hired based on the below qualifications: Associate Director, Clinical Pharmacology PhD with typically 4+ years...Full timeLocal area
- Treeline Biosciences in Watertown, MA seeks an Associate Director/Director of Clinical Pharmacology to lead early development pharmacology strategies, design studies for IND and first-in-human programs, and guide dose selection through PK/PD analyses. This senior scientist...
$170k - $182k
The Associate Director position within Clinical Supply Chain provides strategic leadership and oversight for end-to-end supply chain management across multiple... ..., cross-over) and their implications for supply chain strategy.Demonstrated expertise in global inventory management,...Work at officeLocal areaFlexible hours3 days per week$154.4k - $242.55k
...Strategic Planning Group within PharmSci Clinical Manufacturing Planning, which is... ...across Takeda’s clinical portfolio.The Associate Director contributes to the team’s delivery of... ...capabilities by owning program-level planning strategy, integrating demand, supply, cost, and...Minimum wageTemporary workLocal area$165k - $185k
...hyperoxaluria type 1, progressing into clinical trials, the company continues to... ..., read on.About the Role: The Associate Director, Biomarker and Assay Development will report to the Senior... ...Research, and will lead biomarker strategy, assay development, fit-for-purpose...Work at office$174k - $212k
...well‑understood biology and a clearly defined clinical development and regulatory path, and each... ...Overview Prime Medicine is seeking an experienced Associate Director of Clinical Data Management to lead clinical data strategy and execution across gene editing programs...Full timeTemporary work$174k - $212k
Prime Medicine is seeking an Associate Director of Clinical Data Management in Watertown, MA. This role involves leading clinical data strategy and execution for gene editing. The ideal candidate will have extensive experience in clinical trials and vendor oversight. The...- Real Chemistry seeks an Associate Director, Medical Strategy to join our growing team. You will guide project direction within accounts, collaborate with scientific and medical experts to elevate medical content, and lead teams to deliver high-quality work. This role focuses...Remote job
- Prime Medicine in Watertown, MA, is seeking an Associate Director, Clinical Data Management to drive clinical data strategies for gene editing programs. The candidate will lead internal and external data management activities crucial for IND, CTA, and BLA submissions....
$198.5k - $311.85k
...will inspire you and empower you to shine? Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our... ...OBJECTIVES:The Associate Medical Director leads and drives strategy for clinical studies within the overall global clinical development...Minimum wageTemporary workWork at officeLocal areaRemote workNight shift$167.9k - $260.5k
...outside of the organization.Your Role:The Clinical Pharmacology position in Quantitative... ...Model Informed Drug Development (MIDD) strategies from the early to late-stage clinical development... ...development (5+ years for Scientific Director)Doctorate degree (PhD, PharmD or MD)...Work at officeLocal areaImmediate start- Real Chemistry is seeking an Associate Strategy Director to shape and execute brand strategy across campaigns, reporting to executive leadership and collaborating with cross-functional teams. The role emphasizes growth, brand equity, and client impact. The position is hybrid...Remote work
$133.4k - $238.4k
Job DescriptionThe TAA Revenue Operations team is seeking a Associate Director of Sales Strategy to serve as a strategic business partner to the Divisional General Managers and Sales Leadership. Reporting into Director Revenue Operations TAA division, this role is responsible...Full timeContract workWork at office$152.6k - $283.4k
...medicines. As a Sr Principal Scientist / Associate Director, Biomarker Assay Development Laboratory, you will... ...across drug discovery and clinical development. Working across a diverse... ...development.Design fit-for-purpose assay strategies enabling target engagement,...Full timeContract workLocal areaFlexible hours$146.9k - $262.4k
The Product Management Associate Director, Market Strategy- Compliance Analytics role fills a key spot within the Lending Systems division of Wolters Kluwer Compliance Solutions. This individual will contribute to accelerating growth and developing new strategies to further...Full timeWork at office$230.94k - $255.25k
...Associate Medical Director C4 Therapeutics (C4T) is a clinical-stage biopharmaceutical company dedicated to delivering on the promise of targeted protein degradation... ...biostatistics, to ensure alignment on clinical strategy and study design. Serve as the medical...Flexible hours$174k - $196k
...Associate Director, Clinical Pharmacology Cambridge, Massachusetts, United States Associate Director, Clinical Pharmacology City Therapeutics... ...Sciences Team to help shape the clinical development strategy of our growing portfolio. The Associate Director of Clinical...Work at officeWork from homeFlexible hours- Korro in Cambridge, MA is seeking a senior leader to direct the strategic and operational management of clinical supply across all development phases. You will ensure GMP-compliant, cost-effective delivery of investigational products to global sites and partner with Clinical...
$148k - $236.5k
.... Position Summary:Pioneering Medicines is seeking an Associate Director or Director, Clinical Development Operations to join our growing team and take... ...assessments, country/site selection, and recruitment strategy.Participate meaningfully in dose escalation meetings, DSMB...For contractors- Reportingto:Sr. Director,Clinical Data Management Do you have the passion and commitment to join... ...clinical development programs. The Associate Director will oversee CRO partners and... ...closeout.Develop and execute data management strategies that support program timelines,...2 days per week
$160k - $240k
Who we are:Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to...Contract work$154.4k - $242.55k
...DescriptionOBJECTIVES/PURPOSE: • The Associate Director, GCSC Operations Lead is responsible for... ..., the Associate Director manages Clinical Supply project delivery in support of... ...protocols and to develop supply packaging strategies, timelines, and budgets.Utilizes the Smart...Minimum wageContract workTemporary workLocal areaRemote work$146.3k - $234.1k
...medicine through cutting-edge science and innovation. As Associate Director, Clinical Pharmacology & Pharmacometrics, you will play a pivotal role... ...Collaborating with multidisciplinary teams, you’ll drive strategies that shape the future of transformative therapies for...Hourly payWorldwide- ...at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description Purpose: As Associate Director, AI Strategy and Planning, you are responsible for driving AI strategy and governance across Operations and ensuring alignment with...Full timeLocal area
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