Associate Director, Global Regulatory Lead, Oncology
$154.4k - $242.55kTakeda
Job Description About the role At Takeda, we are a forward‑looking, world‑class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life‑changing therapies to patients worldwide. Takeda is committed to creating better health for people and a brighter future for the world. Guided by our OneOncology vision, we are advancing a rapidly growing oncology portfolio with potentially first‑in‑class and best‑in‑class therapies, including ADCs, complex biologics and small molecules. Our goal is 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, you will define and lead global regulatory strategies for oncology programs, oversee major submissions, and guide cross‑functional teams to bring breakthrough treatments to patients globally. How you will contribute Define, develop, and lead global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. May lead the Global Regulatory Teams (GRTs) for assigned projects. May serve as global and/or regional regulatory lead as a member of a GRT. Primary FDA contact for projects of responsibility. Accountable for all US FDA submissions and approvals of project(s) of responsibility. May act as direct point of contact with health authorities and lead and manage FDA meetings. Define strategies, provide tactical guidance to teams, and collaborate cross‑functionally to ensure the global regulatory strategy is updated and executed, ensuring global regulatory compliance and/or oversee direct reports or junior staff responsible. For the project(s) of responsibility, collaborate with all Takeda regions to ensure a global regulatory strategy is created and executed upon for all projects within area of responsibility. Ensure project team colleagues, line management, and key stakeholders are apprised of developments that may impact regulatory success, exercising sound judgement and communicating in a professional and timely manner. Participate with influence in or lead departmental and cross‑functional task‑for‑ces and initiatives. May partner with global market access colleagues to lead interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable. May lead regulatory assessment as part of due diligence teams for licensing opportunities. Monitor and anticipate trends that impact both the regulatory and access environments to strengthen product development plan(s) and adopt regulatory strategies in a timely manner. Responsible for demonstrating Takeda leadership behaviors. Minimum Requirements / Qualifications Bachelor’s Degree required, scientific discipline strongly preferred, advanced degree in a scientific discipline strongly preferred. 6+ years pharmaceutical industry, inclusive of regulatory and/or related experience. Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, Canada, ROW and post‑marketing a plus. Preferred experience in reviewing, authoring, or managing components of regulatory submissions. Understand and interpret complex scientific issues across multiple projects as it relates to regulatory requirements and strategy. Strong oral and written communications, managing and adhering to timelines, negotiation skills, integrity and adaptability. Demonstrate acceptable skills with increasing independence in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies. Must work well with others and within global teams. Able to bring working teams together for common objectives. Location Boston, MA. This position is currently classified as “hybrid” following Takeda’s Hybrid and Remote Work policy. Compensation & Benefits Summary Base Salary Range $154,400.00 - $242,550.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short‑term and/or long‑term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short‑term and long‑term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well‑being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. #J-18808-Ljbffr Takeda
$208.2k - $327.14k
A leading global R&D organization is seeking a Senior Director, Global Regulatory Lead - Oncology. This role involves leading global regulatory strategy and engaging with cross-functional teams to ensure the success of innovative oncology therapies. The successful candidate...Suggested$208.2k - $327.14k
...our OneOncology vision, we are advancing a rapidly growing oncology portfolio with potentially first-in-class and best-in-... ...lasting impact on patients worldwide. Join Takeda as a Senior Director, Global Regulatory Lead - Oncology, where you will be part of the global...SuggestedMinimum wageFull timeTemporary workLocal areaWorldwide$169.4k - $266.2k
...As a member of Takeda Oncology, your work will... ...best. As part of the Global Medical Affairs Oncology... ...Communications Group Lead, Solid Tumors. As a... ...and deliverables, the Associate Director, Scientific Communications... .... Compliance and Regulatory: Excellent understanding...SuggestedMinimum wageFull timeFor contractorsWork experience placementFreelanceLocal areaRemote work$154.4k - $242.55k
Job Title Lead, Global Pricing, Oncology (Associate Director) Location Cambridge, MA About the role Will lead the development of global pricing strategies and drive operational implementation across multiple launch and in-line assets for the Takeda Oncology Business...SuggestedTemporary workLocal area- Takeda is seeking a Senior Director, Global Regulatory Lead for Oncology in Boston, MA. This role involves leading global regulatory strategy for complex oncology projects, with responsibilities that include overseeing FDA submissions and ensuring compliance with regulatory...Suggested
- Takeda Pharmaceutical in Cambridge, MA is seeking a Lead, Global Pricing, Oncology (Associate Director) to drive pricing strategies for the Oncology Business Unit. This role requires a minimum of 6 years of relevant experience within the pharmaceutical/biotech industry...
$154.4k - $242.55k
...therapies to patients worldwide. This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices... ...as follows: With minimal supervision, develops and leads the execution of regulatory CMC investigational, registration...Minimum wageFull timeTemporary workLocal areaRemote workWorldwide- ...CRISPR Therapeutics is a leading biopharmaceutical... ...cardiovascular, autoimmune, oncology, regenerative... ...Reporting to the Head of Regulatory Affairs, you will... ...collaboration with CMC and global development teams,... ...accomplishments: ~ Associate Director: ~12+ Years of...Contract workRemote work
$157.2k - $256.6k
...Associate Director, Global CMC Regulatory Strategy As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor...Work at officeRemote workWorldwideRelocation package3 days per week$182k
...therapeutic areas including immunology, oncology and neuroscience - and products... .... ( Job Description The Director Regulatory Affairs Global Regulatory Lead (GRL II), Global Regulatory... ...leadership roles in professional associations, industry, and trade groups as appropriate...Local areaWorldwide$196.7k - $353.4k
...The role Moderna is seeking an individual to lead development and execution of global regulatory strategy for programs in its oncology portfolio. This leader will shape regulatory pathways for novel, first-in-class therapeutics and drive successful global development...Permanent employmentWork at officeWork from home- Associate Director, Global Regulatory Affairs, Advertising and Promotion Job Description At Takeda, we are a forward‑looking, world‑class R&D organization... ...Affairs Advertising and Promotion (GRA A&P) Review Lead is accountable for management of all assigned programs/products...Full timeRemote workWorldwide
$174.5k - $274.23k
A leading biotechnology company is seeking a Director, Global Regulatory Lead, GI & Inflammation. The role involves defining global regulatory strategies, leading teams, and ensuring compliance with FDA regulations. Candidates should have over 8 years of pharmaceutical...$154.4k - $242.55k
Dormont Manufacturing Co is seeking an Associate Director, Global and US Pipeline Forecasting Lead to drive the forecast strategy for key pipeline assets in the Oncology Business Unit. This role involves collaborating with multiple stakeholders to provide insights and...$154.4k - $242.55k
Job Description Associate Director, Scientific & Competitive Analysis, Global Oncology Takeda Pharmaceutical Cambridge, MA About the role: This position will be responsible... ...competitive leadership. The role will be leading, creating and delivering integrated insights...Minimum wageFull timeTemporary workLocal area$169.4k - $266.2k
A leading global pharmaceutical company based in Boston is seeking an Associate Director, Medical Review. This role involves providing advanced... ...ensuring compliance with regulatory guidelines. Candidates should... ...a strong preference for oncology expertise. The position offers...$169.4k - $266.2k
Job Description The Associate Director, Medical Review, will serve as... ...across diseases areas for Global Medical Affairs Oncology (GMAO). The individual... ...practice standards, including regulatory guidelines to meet... ...plans to share metrics. Lead the development and maintenance...Minimum wageFull timeTemporary workLocal area$154.4k - $242.55k
Job Title Associate Director, Scientific & Competitive Analysis, Global Oncology Company Takeda Pharmaceutical Location Cambridge, MA Job Overview This position will... ...competitive leadership. The role will lead, create and deliver integrated insights across multiple...Full timeTemporary workLocal areaRemote work- Overview As an Associate Director, Global Regulatory Affairs Marketed Products you will: lead and contribute global strategies to maximize regulatory success for complex and multiple projects; provide strategic and tactical advice to ensure timely development and maintenance...Local area
$270k - $330k
The Senior Director, Global Regulatory Affairs, Oncology is accountable for providing regulatory strategic leadership to assigned program... ...activities with health authorities or trade associations where appropriate, and leads operational excellence initiatives within Global...Temporary workLocal areaWorldwideFlexible hours$142.5k - $256.5k
The Role: The Associate Director, Global Regulatory-CMC will be responsible for coordinating regulatory CMC activities for one or more products, depending... ...all submissions conform to health authority guidelines Lead Regulatory CMC discussions and interactions with health...Permanent employmentWork at officeWork from home$154.4k - $242.55k
Job Description The Associate Director Launch/Pre Launch Forecasting Lead is responsible for driving the forecast strategy for key oncology assets. This role sits within the larger Global Insights and Analytics organization in the Oncology Business Unit (OBU) and is responsible...Minimum wageFull timeTemporary workLocal areaRemote work$169.4k - $266.2k
...drive continual enhancement of GMAO scientific knowledge of Takeda Oncology marketed and pipeline products, relevant disease states, and... ...tailored training packages and plans to address those needs Lead development and updating of high-quality medical affairs education...Minimum wageFull timeTemporary workLocal areaRemote work$137k - $215.27k
Initial Therapeutics, Inc. is looking for a professional in Boston, MA, to contribute to Global Regulatory Affairs CMC. The role requires 6+ years of regulatory CMC or Device experience and a BS/BA degree in a scientific discipline. Responsibilities include executing regulatory...- A leading oncology biotech company in Boston seeks an Executive Director of Global Regulatory Affairs. This crucial role involves providing strategic regulatory leadership for oncology programs, ensuring compliance, and overseeing global regulatory strategies. The ideal...
- AstraZeneca is seeking a Senior Regulatory Affairs Director in Boston, MA to lead global regulatory strategy for oncology programs. The role involves overseeing a Global Regulatory Strategy Team and ensuring competitive labeling. The ideal candidate has an advanced degree...Work at officeRemote work
- Moderna is seeking a seasoned regulatory leader to develop and execute global regulatory strategies for its oncology portfolio. This role involves leading regulatory submissions, negotiations with health authorities, and shaping strategies for novel therapeutics. The ideal...
- Allergan is seeking a Director of Regulatory Affairs to develop and implement global regulatory strategies to secure product approvals. The role involves leading the Global Regulatory Product Team and requires strong leadership experience within the pharmaceutical sector...
- Vertex Pharmaceuticals Inc (US) in Boston is seeking a Regulatory Strategy Associate Director to oversee the development of global regulatory strategies for their portfolio. The role involves leading regulatory submissions and mentoring team members on regulatory frameworks...
$169.4k - $266.2k
...Manufacturing Co is seeking a training specialist for Medical Affairs in Boston, MA. This hybrid role requires strong expertise in oncology and strategies for developing tailored training programs. You'll collaborate with teams to identify learning needs and ensure...
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