Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Associate Director, Global RA Labeling Lead

Synectics Inc

Job Description

Job Description

Description:

  • The Plasma-Derived Therapies (PDT) R&D Organization is dedicated to bringing forward new plasma-derived therapies for patients with immunologic, hematologic, and other complex diseases.

  • There are two main drivers of innovation that are the focus of the PDT R&D organization: Translational Pharmaceutical Sciences and Precision Medicine

  • The Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU) is a key role in Global Labeling and works under the direction of the Head of Global Labeling and is:

  • Providing regulatory expertise, strategic insight, and guidance to internal stakeholders, including Clinical, Pharmacovigilance, Legal, Scientific, Commercial, to ensure successful development and maintenance of labeling managed within PDT BU's Global Labeling function, pertaining to pharmaceutical drug and device.

  • Ensuring that there is strategic labeling input in the implementation of regulatory strategies and liaises with regulatory team members in evolving submission and negotiation plans.

  • Formulating regulatory labeling strategies for implementation of new and revised prescribing information and packaging; strategically interprets scientific, medical, and regulatory data and information.

  • Providing expert advice on current labeling requirements, templates, tools, and Health Author-ity-issued guidance pertaining to pharmaceutical drug and device.

  • Drives labeling strategy for the PDT BU via the development and lifecycle management of the CCDS, US, and EU labels.

  • Formulates and implements innovative regulatory strategies for labeling development to support successful commercialization of developmental products and enhance opportunity for marketed products and global expansion.

  • Prepares strategic labeling vision for early development programs and gains alignment from internal stakeholders.

  • Draws on labeling precedent, Health Authority feedback, and guidance, to create innovative labeling strategies.

  • Provides guidance on combination product/drug-device labeling.

  • Interprets scientific and clinical data and leads development of labeling to optimize product potential and patient benefit-risk ratio.

  • Introduces creative solutions for data presentation and gains consensus by labeling teams to meet the requirements of the Health Authorities

  • Prepares backup strategies in support of labeling negotiations.

  • Takes initiative in leading global labeling team and cross-functional projects.

  • Leads CCDS, US, and EU Labeling Teams in the development and maintenance of labeling.

  • Actively engages cross-functional labeling stakeholders to gain consensus on labeling strategy.

  • Effectively identifies and resolves conflicts/issues to reach labeling decisions with minimal escalation to management for dispute resolution.

  • Liaises with Regulatory Intelligence to maintain awareness of regulatory legislation pertaining to labeling and communicates the impact on the PDT BU products.

  • Provides guidance to Regulatory affiliates as necessary in assessment of labeling changes to ensure timely implementation.

  • Oversees the direction, management and implementation of the labeling processes, templates, tools and systems to improve efficiency, productivity and quality and consistency across products and compliance with regulatory labeling guidance.

  • Project manages new or updated labeling to ensure compliance with internal procedural or Health Authority submission timelines.

  • Manages and facilitates review of CCDSs and regional labeling, as appropriate, via the Labeling Team and executive governance committees for PDT BU products.

  • Prepares final proposed labeling for review by the Labeling Team and approval by the executive governance committees, as appropriate, prior to internal approval and/or submission to health authorities.

  • Manages the preparation of submission-ready labeling components, consults with affiliates on

  • Health Authority communications regarding labeling.

  • Ensures internal and external stakeholder awareness of proposed and newly approved labeling changes, as required.

  • Ensures compliant version control of product labeling and other related documentation within the document management systems.

  • Ensures QC of CCDSs and other labeling documents.

  • Updates labeling decision records to ensure labeling history is appropriately tracked and archived.

  • Designs and delivers labeling training programs.

  • Documents labeling tracking information in end to end tracking systems to facilitate overall compliance and oversight of labeling activities

  • Leadership

    • Ability to motivate, mentor and manage diverse cross functional teams

    • Global perspective with a demonstrated ability to work across functions, regions, and cultures

    • Ability to identify potential challenges and opportunities and make recommendations

    • Proven skills as an effective collaborator who can engender credibility and confidence within and outside the company

    • Valuing and promoting differences by embracing and demonstrating a diversity and inclusion mindset and models these behaviors for the organization

    • Invests in helping others learn and succeed

    • Able to influence without authority at senior level (TET/TET-1, GLOC)

    • Demonstrates agile leadership by seeking to understand with the ability to evolve ideas as needed.

    • Interviews, mentors, and develops employees/consultants.

    • Builds and enhances strategic, cross-functional, stakeholder relationships through thoughtful engagement and leadership (including, the planning, assigning, and direction of work).

  • Decision-making and Autonomy

    • Accountable for acting decisively and exercise sound judgment in making decisions with limited information

    • Accountable for making clear business arguments and strategic recommendations leveraging both quantitative and qualitative evidence

    • High ability to seek diverse input by balancing multiple internal and external multiple stakeholders to drive solutions and set priorities

    • High ability to incorporate feedback and ensure decisions are made swiftly to enable flawless execution

    • Develops executable plans and meets budget and deadlines

    • Builds a culture of data driven decisions

    • High ability to challenge self and others to overcome barriers and deliver high quality solutions to the business.

    • Crisp decision-making following appropriate consultation, even in times of ambiguity.

    • Self-starter. Demonstrates initiative in advancing strategic projects with minimal guidance.

  • Interaction

    • Organizational savvy and leverages internal network to enable alignment and effective execution in and outside the BU

    • Valuing and promoting differences by recognizing the importance of connections and brings in key stakeholders to work towards the best possible solutions

    • Strong communicator, able to persuasively convey ideas verbally and in writing

    • Innovation (The required level of scientific knowledge, knowledge sharing, innovation and risk-taking)

    • Disruptive thinker with the ability to influence and change how RnD used data to make decisions and set priorities

    • Continuously challenging the status quo and bringing forward innovative solutions

    • Ability to identify areas for process and systems innovation and implement change that will enhance the overall effectiveness of the team.

  • Complexity

    • Delivers solutions to abstract problems across functional areas of the business.

    • Identifies and solves fundamental issues for major functional areas through assessment of intangible variables.

    • Recommends key decisions, escalates key issues per agreed governance framework, and persuades key stakeholders through influencing skills.

    • Creates clarity of accountabilities in a global and highly matrixed organization, with a high degree of complexity

    • Ability to provide data that will resolve or simplifies complexity between commercial, operations, and strategy

    • Resilient and comfortable working through large scale global change management

    • Knowledge of the global drug discovery and development process, laws and regulations affecting biopharmaceutical development in US, EU and international markets.

  • The primary focus of this role is biologics, with experience in plasma-derived products considered a bonus. The individual will be responsible for developing Target Label Profiles (TLPs) and leading labeling strategy for Company Core Data Sheets (CCDSs), U.S. Prescribing Information (USPI), and Summary of Product Characteristics (SmPC) updates

  • The Labeling Strategist will lead cross-functional Label Working Groups to drive alignment across stakeholders, develop labeling recommendations, and present proposals to the Global Labeling Oversight Committee for review and endorsement.

  • Team Structure: Currently there are four Labeling Strategists. The strategy team is supported by Labeling Operations Leads, as well as the broader Global Regulatory Affairs organization, to ensure successful planning and execution of labeling initiatives.

Qualification:

  • Bachelor's or Master's degree required.

  • Minimum of 7-10 years of experience in the biopharmaceutical industry (e.g., safety, ad promo, regulatory strategy, medical affairs, etc.).

  • 5-7 years of direct experience in a global, US, or EU labelling role is desired.

  • Experience in plasma-derived therapies and biologics preferred.

  • Advanced scientific or health sciences degree or equivalent relevant experience preferred.

  • Previous leadership experience and management of direct reports preferred.

  • Must have a detailed understanding of pharmaceutical drug and device development and global regulations pertaining to labeling, specifically, EU and US labeling requirements and guidance.

  • Combination product/drug-device labeling knowledge is preferred.

  • Advertising and promotion knowledge is a plus.

  • Expertise in the development and maintenance of the Company Core Data Sheet, the USPI, and the EU SmPC.

  • Understanding of SPL format, requirements and guidance for legacy and PLR labels.

  • Proficiency in Electronic Document Management Systems and End-to-End (E2E) Labeling

  • Tracking Systems to support labeling documentation, tracking, and compliance activities.

Benefits:

Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics.

Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.

Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.

401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first of the month following at least 1 calendar year after employment begins.

Synectics is an equal opportunity employer.

\nCompany Description

Synectics is a leading staffing and workforce solutions company dedicated to connecting exceptional talent with top organizations. We specialize in IT, engineering, finance, healthcare, and professional services recruitment, offering both contract and permanent staffing solutions. With a people-first approach, we focus on understanding the unique needs of our clients and candidates to create long-term, successful matches. Our mission is to empower businesses with the right talent while helping professionals achieve rewarding career opportunities

Company Description

Synectics is a leading staffing and workforce solutions company dedicated to connecting exceptional talent with top organizations. We specialize in IT, engineering, finance, healthcare, and professional services recruitment, offering both contract and permanent staffing solutions. With a people-first approach, we focus on understanding the unique needs of our clients and candidates to create long-term, successful matches. Our mission is to empower businesses with the right talent while helping professionals achieve rewarding career opportunities

Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Associate Director, Global RA Labeling Lead in Cambridge, MA vacancy
  • $154.4k - $242.55k

     ...the focus of the PDT R&D organization: Translational Pharmaceutical Sciences and Precision MedicineThe Global Regulatory Labeling Strategy Lead (Associate Director), Plasma-Derived Therapies Business Unit (PDT BU) is a key role in Global Labeling and works under the direction... 
    Suggested
    Minimum wage
    Temporary work
    Local area

    Takeda

    Cambridge, MA
    5 days ago
  • $100 per hour

    job summary: If you thrive on steering high-stakes global labeling strategy-from CCDS creation to FDA and EMA negotiations-this is your...  ...changing plasma therapies and drug-device combination products, leading cross-functional teams and cutting through complexity to... 
    Suggested
    Hourly pay
    Contract work
    Temporary work
    Work experience placement
    Worldwide
    Cambridge, MA
    4 days ago
  • $154.4k - $242.55k

     ...focused, innovation-driven company to inspire you and empower you to shine? Join us as Global Biomarker Lead, Inflammation, GI2 TAU based in Cambridge, MA reporting to the Senior Director, Head Inflammation Biomarkers, ED&B GI2 TAU.At Takeda, we are transforming the... 
    Suggested
    Minimum wage
    Temporary work
    Local area

    Takeda

    Boston, MA
    5 days ago
  • $173.2k - $216.5k

     ...WellnessSupport for CaregiversFor a full list of our comprehensive benefits, see our website: The Importance of the Role The Associate Director, Global Medical Affairs Lead (GMAL) is a key contributor to the GMAL team within Global Medical Affairs (GMA) department. As GMALs, we drive... 
    Suggested
    Full time

    Sarepta Therapeutics

    Cambridge, MA
    4 days ago
  • $154.4k - $242.55k

     ...to accelerate access to transformative medicines and make a lasting impact on patients worldwide.Join Takeda as Associate Director, Global Regulatory Lead Oncology where you will be part of the global regulatory team. As Associate Director, Global Regulatory Lead Oncology... 
    Suggested
    Minimum wage
    Local area
    Remote work
    Worldwide

    Takeda

    Boston, MA
    3 days ago
  • $154.4k - $242.55k

     ...employment application is true to the best of my knowledge.Job DescriptionLead, Global Pricing, Oncology (Associate Director)Takeda PharmaceuticalCambridge, MAAbout the role:This role will lead the development of global pricing strategies and drive operational... 
    Minimum wage
    Temporary work
    Local area
    Remote work

    Takeda

    Boston, MA
    5 days ago
  • $169.4k - $266.2k

     ...career grounded in purpose and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Director, Global Scientific Communications Group Lead. This is a hybrid role based in Cambridge, MA.As a subject matter expert on... 
    Minimum wage
    Temporary work
    For contractors
    Freelance
    Local area
    Remote work

    Takeda

    Cambridge, MA
    4 days ago
  • $163.2k - $244.8k

    Job DescriptionGeneral Summary:The Associate Director, Global Submission Management (GSM) is responsible for the strategic...  ...role partners closely with Major Submission Leads, Global Regulatory Strategy, Regulatory CMC, Labeling, Publishing, and Advertising & Promotion... 
    Full time
    Summer work
    Remote work
    Flexible hours
    2 days per week

    Vertex Pharmaceuticals

    Boston, MA
    7 days ago
  • $152k - $209k

     ...and a member of myGwork – the largest global platform for the LGBTQ+ business community...  ...in neuroscience. The role of the Associate Director requires the ability to provide regulatory...  ...materials are consistent with FDA-approved labeling, compliant with applicable FDA... 
    Full time
    Temporary work
    Work at office
    Local area

    Biogen

    Cambridge, MA
    4 days ago
  • $154.4k - $242.55k

     ...patients worldwide.This role is within the Global Regulatory Affairs (GRA) Chemistry...  ...follows: With minimal supervision, develops and leads the execution of regulatory CMC investigational...  ...strategies for assigned products. RA CMC member on the Global Regulatory CMC team... 
    Minimum wage
    Temporary work
    Local area
    Remote work
    Worldwide

    Takeda

    Boston, MA
    5 days ago
  • Overview The Associate Director, Downstream, Emerging Modalities, is expected to provide technical...  ...(AOC) purification as well as lead program(s) with the goal to enable transition...  ...commitment to people. We're proud to be a globally recognized top employer, where an... 
    Full time
    Temporary work
    Local area
    Flexible hours

    Alnylam Pharmaceuticals

    Cambridge, MA
    6 days ago
  • $183.77k - $275.65k

     ...Job Title: Translational Medicine Lead, Associate Director, Oncology Location: Cambridge, MA Introduction to role: Are you ready to...  ...In this hands-on, collaborative role you will lead across a global matrix, converting complex data into practical recommendations... 
    Hourly pay
    Temporary work
    Work at office
    Flexible hours
    3 days per week
    Cambridge, MA
    16 days ago
  • $161.5k - $218.5k

     ...PharmaceuticalsPosted: 2026-08-16Overview The Associate Director, Medical Education Marketing, US Congress and TLL Asset Lead will lead national strategy and execution for...  ...commitment to people. We're proud to be a globally recognized top employer, wherean authentic, inclusive... 
    Full time
    Temporary work
    Local area

    Alnylam Pharmaceuticals

    Cambridge, MA
    7 days ago
  • $135k - $225k

     ...to our communities.What You Will Do:The Global Market Access team provides...  ...across major and emerging global markets.Associate Directors are key members of the Global Market Access...  ...include:Track record of success developing, leading, and delivering global (e.g., EU, APAC,... 
    Full time
    Work experience placement
    Immediate start
    Remote work
    Flexible hours

    Guidehouse

    Boston, MA
    5 days ago
  • $192.4k - $302.39k

     ...application is true to the best of my knowledge.Job DescriptionThe Global Medical Affairs Lead, PDT Immunology is responsible for co-leading the...  ...is preferredExperience in field-based roles (e.g. Medical Director, Medical Science Liaison) is a plusExperience in clinical... 
    Minimum wage
    Local area
    Remote work

    Takeda

    Cambridge, MA
    3 days ago
  • $212k - $333.19k

     ...of my knowledge.Job DescriptionAbout the role:The Senior Director, Oncology Search & Evaluation will be responsible for advancing...  ...and commercial judgment, and a demonstrated ability to lead in a highly matrixed global environment. You will report to the Head, NPP and S&E OBU... 
    Minimum wage
    Local area
    Remote work

    Takeda

    Cambridge, MA
    4 days ago
  • $192.4k - $302.39k

     ...you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Director, Global Medical Lead, Zasocitinib- Psoriatic Arthritis (PsA) in our Cambridge, MA office.At Takeda, we are transforming the pharmaceutical... 
    Minimum wage
    Work at office
    Local area
    Remote work

    Takeda

    Cambridge, MA
    5 days ago
  • $328k

     ...DescriptionGeneral Summary:The Executive Medical Director, Global Medical Lead (GML), Pain is a critical leadership...  ...management of funds allocation, and associated tracking to ensure alignment with...  ...product Represent Medical Affairs in label discussions Support Access, Patient... 
    Full time
    Summer work
    Remote work
    Flexible hours
    2 days per week

    Vertex Pharmaceuticals

    Boston, MA
    5 days ago
  • $154.4k - $242.55k

     ...to the best of my knowledge.Job DescriptionAbout the role:As part of the Global Oncology Products & Pipeline Strategy (GOPPS) global marketing team, the Global Marketing Lead, Associate Director reports to the Head of GI Oncology and works in the gastric cancer and/or... 
    Minimum wage
    Local area
    Remote work

    Takeda

    Boston, MA
    7 days ago
  • $154.4k - $242.55k

     ...submit in my employment application is true to the best of my knowledge.Job DescriptionAbout the role:The Associate Director, Global and US Pipeline Forecasting Lead is responsible for driving the forecast strategy for key pipeline assets. This role sits within the... 
    Minimum wage
    Local area
    Remote work

    Takeda

    Boston, MA
    4 days ago
  • $150k - $200k

     ...The Associate Director, Advertising and Promotion Compliance,...  ...the Regulatory Affairs (RA) representative for assigned...  ...ensuring adherence to global compliance standards...  ...and Promotional Labeling Branch (APLB) for assigned...  ..., and autonomy of a leading biotech. You’ll join an... 
    Temporary work
    Work at office
    Flexible hours
    3 days per week
    Boston, MA
    27 days ago
  • Job title: Global Associate Director, HCP Education and Engagement Strategy - IgG4-RD Location: Cambridge, MA Travel Expected: 25%About the Job:...  ...and clinical readiness ahead of launch.The individual will lead global KOL identification, mapping, and engagement strategy... 

    Sanofi

    Cambridge, MA
    4 days ago
  • Senior Director, Global Regulatory Lead, GI & Inflammation About the role: The Global Regulatory Leads, Senior Director is responsible for ensuring...  ...(GRTs) and applicable sub-working groups, such as the Label Working Group, and represents GRTs at project team meetings... 
    Full time
    Local area

    Takeda

    Cambridge, MA
    5 days ago
  • $163k - $225k

     ...inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not...  ...Technology (PO&T) Division is looking to hire a CMC Asset Lead. This Associate Director level Asset Lead is a member of the Asset Development & Portfolio... 
    Full time
    Temporary work
    Local area

    Biogen

    Cambridge, MA
    22 hours ago
  • $190.8k - $300.3k

     ...and sustain reliable end-to-end execution through steady-state operations following potential FDA approval.The Associate Director Oncology Treatment Site Lead (TSL) is the primary field-based point of contact for operational information and support for product treatment... 
    Full time
    For contractors
    Local area
    Flexible hours

    Merck Sharp & Dohme (MSD)

    Boston, MA
    4 days ago
  • $167k - $286k

     ...86,000Company: Wave Life SciencesPosted: 2026-09-01Director/Associate Director, Platform and Pipeline Medical Affairs LeadWave Life Sciences...  .... Driven by the calling to "Reimagine Possible", we are leading the charge toward a world in which human potential is no longer... 
    Contract work
    Temporary work
    Summer work
    Work at office
    Local area

    Wave Life Sciences

    Cambridge, MA
    2 days ago
  • About the role The Senior Director, Oncology Search & Evaluation will advance the oncology...  ...opportunities (discovery through commercial). Lead scientific, strategic, and commercial...  ...medical/partnering forums. Lead/influence global cross-functional teams in a matrixed... 

    Scorpion Therapeutics

    Cambridge, MA
    5 days ago
  • $210.9k - $379.2k

     ...colleagues and strategic partners worldwide, contributing to global health initiatives.Moderna's commitment to advancing the technological...  ...' lives worldwide.Moderna is seeking a Global Medical Director to lead medical affairs strategy across our Oncology portfolio,... 
    Permanent employment
    Full time
    Work at office
    Work from home
    Worldwide

    Moderna Therapeutics

    Cambridge, MA
    7 days ago
  • $192.4k - $302.39k

     ...DescriptionAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Global Medical Lead, Nephrology in our Cambridge, MA office.At Takeda, we are transforming the pharmaceutical industry through our R&D-driven... 
    Minimum wage
    Temporary work
    Work at office
    Local area
    Remote work

    Takeda

    Boston, MA
    5 days ago
  • $192.4k - $302.39k

     ...and empower you to shine? Join us as a Global Medical Lead, PDT Hematology (f/m/x) in our...  ...Hematology with focus on Prothromplex and associated global medical activities for the entire...  ...consult with Quality, Regulatory, Medical Director.Maintain knowledge base as to... 
    Minimum wage
    Temporary work
    Work experience placement
    Work at office
    Local area
    Remote work

    Takeda

    Cambridge, MA
    5 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Associate Director, Global RA Labeling Lead. Be the first to apply!