1. Your Initial Application
Once you’ve found a job that’s right for you, follow the instructions on screen and submit the information required.
Testing Laboratory Opportunities
Medical Director - Pharmacovigilance (PV), Global Medical Safety
Boston, MassachusettsBy 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’sPrivacy Noticeand 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
Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Medical Director - Pharmacovigilance (PV) for our Global Medical Safety team in our Cambridge, Massachusetts office.
OBJECTIVE:
- Support marketed products: Responsible for the oversight of signal detection and risk management activities for designated global/regional product(s)
- Support Therapeutic Lead: Flexible to support compounds/initiatives outside of primary therapeutic area(s) as directed by business and departmental needs
ACCOUNTABILITIES:
- Expectation of GSL role for marketed compound(s) in close association with the TAL
- Company-wide safety expert for his/her compound responsibilities
- Intimate knowledge of safety, including any emerging safety concerns and risk/benefit profile for ‘own’ compounds with input for other compounds as needed
- Serving in a leadership capacity for complex and strategically important programs
- Responsible for development of documents and for negotiation with Regulatory authorities on safety matters involving these compounds. This includes but is not limited to: direct interaction with Regulatory authorities, expertise in preparing regulatory responses to Pharmacovigilance Risk Assessment Committee (PRAC) and other health authorities, authorship of safety summaries to support changes to the PI/SmPC, significant contribution to MAAs and NDAs, authorship of Executive Summaries on special safety topics, authorship of Integrated Analyses of Safety (IAS) for CTDs, etc.
- Training and mentoring of Pharmacovigilance Physicians and Specialists
- Perform activities required to serve as Global PV physician:
- Review and oversight of safety data, both non-clinical and clinical
- Review and/or sign off of protocols, SAPs, clinical study reports, IBs, IMPD and other documents developed for submission to regulatory authorities
- Interactions with external experts and regulatory agencies and partner/co-development companies
- Authorship and sign off of Safety Monitoring Plan/Risk Management Plan
- Lead data analysis and writing of regulatory submission documents, for license application and variation activities and for safety issues and questions from regulators
- Direct the set-up of safety procedures and development of safety exchange agreements for co-development projects
- Maintain professional knowledge and accreditation by active participation in continuing medical education activities
EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:
- Qualified physician (License, e.g. GMC registered, preferred)
- Minimum of 8 years of experience in pharmacovigilance, clinical research or clinical development
- 2-3 years clinical experience with patients following post-graduate training with significant knowledge of general medicine
- Knowledge of principles of epidemiology and statistics.
- Critical thinking and analytical skills and ability to make high level decisions
- Excellent oral and written communication skills including ability to present to large internal/external groups
- Good level of computer literacy with Microsoft applications
This job posting excludes CO applicants
WHAT TAKEDA CAN OFFER YOU:
- 401(k) with company match and Annual Retirement Contribution Plan
- Tuition reimbursement
- Company match of charitable contributions
- Health & Wellness programs including onsite flu shots and health screenings
Locations
Boston, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Applying Here
We want to make your application process as simple and streamlined as possible.
2. Your First Review
One of our Hiring Managers will review your application and reach out to you if we think you’re a good fit.
3. Your First Interview
We’ll arrange a time for us to meet virtually or in person. Depending on the role and market, there may be more than one interview.
4. Job Offer
If you’re successful in the interview process, we’ll get in touch with you to make a job offer.
5. Pre-Employment
After electronically accepting your offer, you’ll receive communications electronically which will guide you through the pre-employment process.
6. Onboarding
Once you complete the pre-employment process, we’ll arrange a date for you to join the team, with an onboarding session taking place in your first few weeks at the company.
Jobs For You
- Senior Medical Director, GPSE Boston, Massachusetts
- Medical Director - Pharmacovigilance (PV) - Marketed Products, Global Medical Safety Boston, Massachusetts
- Medical Director Pharmacovigilance Boston, Massachusetts
- Medical Director, Pharmacovigilance (PV) - NeuroScience Boston, Massachusetts
Job Alerts
Let's Connect
Sign up for our job alerts, and we’ll send opportunities that match your skills right to your inbox. Just enter your information, including uploading your resume.