Takeda Logo

Takeda

Medical Director, Gastrointestinal & Inflammation (Remote)

Posted 2 Hours Ago
Be an Early Applicant
Remote or Hybrid
Hiring Remotely in Boston, MA
228K-359K Annually
Senior level
Remote or Hybrid
Hiring Remotely in Boston, MA
228K-359K Annually
Senior level
The Medical Director oversees safety strategy for pharmaceutical products, leads safety teams, analyzes safety data, and interacts with regulatory authorities ensuring compliance and risk management.
The summary above was generated by AI
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
Objective:
Principal responsibilities include:
  • Serves as Global Safety Lead (GSL) and the Company-wide patient safety expert for assigned pharmaceutical / biological / drug-device combined products, accountable for the safety strategy and major safety deliverables for each assigned product.
  • Leads GPSE Safety Team (GST) and Safety Management Team (SMT) for assigned compounds and products.
  • Represents the cross-functional program team as a product safety profile and risk mitigation expert for internal (e.g., Takeda Safety Board) and external (e.g., Independent Data Monitoring Committee) stakeholders.
  • Manages cross-functional assessment of benefit-risk profile and communication of safety information for assigned compounds and products.

Accountabilities:
  • Analyze and interpret safety data from various sources including non-clinical, clinical, post-marketing and scientific literature.
  • Conduct signal detection, monitoring, evaluation, interpretation, and management for assigned compounds and products.
  • Develop strategy for and lead preparation of responses to safety-related inquiries from regulatory agencies and ethics committees.
  • Ensure communication of all safety information that may impact the benefit-risk profile of assigned products to senior management.
  • Provide medical safety expertise, medical interpretation, review, and authorship of appropriate sections for critical documents (e.g., protocols and amendments, ICFs, IBs, IMPDs, clinical research reports, Health Hazard Evaluations, Signal Evaluation Reports, INDs, NDAs, BLAs, and CTAs) in collaboration with cross-functional colleagues.
  • Provide patient safety input to the clinical development program for assigned products and development compounds, and represent GPSE on internal governance bodies for study protocols, statistical analysis plans and other clinical study-related documents as applicable.
  • Manage benefit-risk profile, including authoring and updating of the benefit-risk documents, e.g., RMPs, for assigned compounds and products.
  • Collaborate and communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs, Quality Assurance, Medical Affairs, Marketing, Manufacturing, and Legal.
  • Interact with Regulatory Authorities as part of a cross-functional team to submit and defend regulatory inquires, MAAs, NDAs, and BLAs.
  • Ensure up-to-date representation of safety information in Company Core Data Sheet (including Reference Safety Information) and Investigator Brochure, as well as other labeling documents.
  • Demonstrate knowledge of local and global health authority requirements.
  • Support GPSE in the maintenance of a highly effective global safety organization in full compliance to worldwide regulations.
  • Train and mentor Pharmacovigilance Physicians and Specialists.
  • Maintain professional knowledge and accreditation by active participation in continuing medical education activities, and fosters a community of continual learning.

Qualifications:
  • M.D. or D.O. or internationally recognized equivalent, with direct clinical experience in patient care following post-graduate training and appropriate grounding and knowledge of general medicine. Board certification and licensure preferred.
  • At least 5 years of experience in pharmaceutical industry within Drug Safety/Pharmacovigilance, with both investigational and marketed products.
  • At least 3 years of experience with aggregate reporting, safety surveillance, signal management and/or risk management.
  • Knowledge and understanding of national and international PV and regulatory guidelines.

Travel Requirements: Local and international travel across Takeda sites may be required.
Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
Massachusetts - Virtual
U.S. Base Salary Range:
$228,200.00 - $358,600.00
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.
Locations
Massachusetts - Virtual
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Exempt
Yes
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
#LI-Remote

Top Skills

Clinical Data Analysis
Pharmaceutical Products
Regulatory Guidelines

Similar Jobs at Takeda

Yesterday
Remote or Hybrid
Boston, MA, USA
258K-405K Annually
Senior level
258K-405K Annually
Senior level
Healthtech • Software • Analytics • Biotech • Pharmaceutical • Manufacturing
The Senior Medical Director oversees medical safety activities for GI and inflammation products, leads safety teams, and manages global safety leaders, ensuring compliance with safety regulations and effective risk assessment.
Yesterday
Remote or Hybrid
Boston, MA, USA
258K-405K Annually
Senior level
258K-405K Annually
Senior level
Healthtech • Software • Analytics • Biotech • Pharmaceutical • Manufacturing
The Senior Medical Director oversees medical safety activities for GI and inflammation products, leads safety teams, and manages global safety leaders, ensuring compliance with safety regulations and effective risk assessment.
Yesterday
Remote or Hybrid
Boston, MA, USA
154K-241K Annually
Senior level
154K-241K Annually
Senior level
Healthtech • Software • Analytics • Biotech • Pharmaceutical • Manufacturing
The Associate Director will develop and implement labeling content and strategy, manage cross-functional teams, author labeling documents, and ensure compliance with regulations for assigned products.
Top Skills: LabelingProject ManagementRegulatory Submissions

What you need to know about the Colorado Tech Scene

With a business-friendly climate and research universities like CU Boulder and Colorado State, Colorado has made a name for itself as a startup ecosystem. The state boasts a skilled workforce and high quality of life thanks to its affordable housing, vibrant cultural scene and unparalleled opportunities for outdoor recreation. Colorado is also home to the National Renewable Energy Laboratory, helping cement its status as a hub for renewable energy innovation.

Key Facts About Colorado Tech

  • Number of Tech Workers: 260,000; 8.5% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Lockheed Martin, Century Link, Comcast, BAE Systems, Level 3
  • Key Industries: Software, artificial intelligence, aerospace, e-commerce, fintech, healthtech
  • Funding Landscape: $4.9 billion in VC funding in 2024 (Pitchbook)
  • Notable Investors: Access Venture Partners, Ridgeline Ventures, Techstars, Blackhorn Ventures
  • Research Centers and Universities: Colorado School of Mines, University of Colorado Boulder, University of Denver, Colorado State University, Mesa Laboratory, Space Science Institute, National Center for Atmospheric Research, National Renewable Energy Laboratory, Gottlieb Institute

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account