Principal Pharmacovigilance Scientist Job at Takeda Pharmaceutical Company Limited, Boston, MA

NmF2YUVnYjhyeVlNK0lWL0x0YjY2OW5oanc9PQ==
  • Takeda Pharmaceutical Company Limited
  • Boston, MA

Job Description

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.

Pursuant to Section 20 C.F.R. 656.10, you are hereby notified that an application for Alien Employment Certification will be filed by Takeda Development Center Americas, Inc. for the following job opportunity:

JOB LOCATION: Cambridge, MA

POSITION : Principal Pharmacovigilance Scientist

POSITION DESCRIPTION : Takeda Development Center Americas, Inc. is seeking a Principal Pharmacovigilance Scientist with the following duties: Facilitate ongoing safety surveillance for assigned products, assisting with data collection and assessment for GST and SMT; Coordinate and perform signal identification, evaluation and management activities for assigned products; Assist with authoring safety evaluations, defining scope and methodology, and providing background information for aggregate safety reports; Assist with conducting preliminary safety analyses and prepare ad hoc reports including Health Hazard Evaluations, Signal Evaluation Reports, and Health Authority responses; Contribute to safety-related deliverables associated with new drug applications, benefit-risk assessments and activities related to risk minimization including RMPs; Liaise with colleagues in relevant functional areas within and outside of GPSE to gather and provide input for appropriate sections of critical documents (e.g., protocols, ICFs, IBs, etc.); Assist with the presentation of patient safety risks and SMT recommendations on safety issues to cross-functional decision-making bodies (e.g., Takeda Safety Board); Build and maintain in-depth knowledge and understanding of designated products/studies, and close knowledge of protocols to effectively respond to safety issues; Ensure up-to-date representation of safety information in CCDS (including RSI) and IB, as well as other labelling documents; Support GPSE in the maintenance of a highly effective global safety organization in full compliance to worldwide regulations. 10% domestic travel required. 100% telecommuting allowed from anywhere in the U.S.

REQUIREMENTS: Bachelor's degree in Pharmacy, Biology, Biochemistry, Pharmaceutical Sciences, Public Health, or health care related field plus 5 years of Pharmacovigilance (PV) related experience. Prior experience must include: Review, analyze, interpret and present complex safety data utilizing data visualization tools to a high standard, with keen attention to detail; Perform data compilation, identify and evaluate new safety signals and trends by conducting systematic reviews of aggregate data and provide conclusions for aggregate safety documents consistent with global regulatory requirements; Author aggregate safety reports such as DSUR (Development Safety Update Report), PSUR (Periodic Safety Update Report)/PBRER (Periodic Benefit-Risk Evaluation Report), PADER (Periodic Adverse Drug Experience Report), RMP (Risk Management Plan) etc., utilizing guidelines such as ICH (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use), GVP (Good Pharmacovigilance Practice) modules V &VII; Query and generate the safety data reports from the PV safety database (ARGUS) and utilize data visualization dashboards such as Empirica; Compile strategies for safety data retrieval by utilizing adverse event coding in MedDRA; Oversee PV safety reporting activities with a thorough understanding of PV regulations (FDA [Food and Drug Administration], EMA [European Medicines Agency], Health Canada, GVP [Guideline on Good Pharmacovigilance Practices modules], ICH [International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use] and global regulatory requirements.

Full time. $111,800 - $191,600 per year. Competitive compensation and benefits.

Qualified applicants can apply at . Please reference job # R0150652. EOE

Any individual may provide documentary evidence bearing on this application, with information on available workers and information on wages and working conditions, to the Certifying Officer, U.S. Department of Labor, Employment and Training Administration, Office of Foreign Labor Certification, 200 Constitution Avenue, NW, Room N-5311, Washington, DC 20210.

Locations
Boston, MA

Worker Type
Employee

Worker Sub-Type
Regular

Time Type
Full time

Job Tags

Full time, Remote job, Worldwide,

Similar Jobs

Trinity Health

Neurology- Physician- Waterloo/CF- $125K Bonuses Job at Trinity Health

 ...Employment Type Full time Shift Description: MercyOne Waterloo Neurology Seeking clinic-based neurologist Join an established practice with two neurologists and one neuro-hospitalist. Neurology clinic shared call with nurse triage only; NO hospital... 

Milltown Pharmacy

Pharmacy Clerk Job at Milltown Pharmacy

 ...We are seeking a Pharmacy Clerk to become a part of our team! The successful candidate will also be responsible for the promotion and representation of us. Engage customers in face-to-face discussions to promote the pharmacy. We are looking for a candidate who is assertive... 

Bath Concepts Independent Dealers

Marketing Coordinator, Windows Direct USA Job at Bath Concepts Independent Dealers

 ...Marketing Coordinator Pay: $40,000.00 - $50,000 per year Job description: Overview: We are seeking a creative Marketing Coordinator to lead content creation, manage our social media presence, and assist in driving our organic growth and brand awareness. The... 

TheraEd Staffing Group

Special Education Teacher - School SPED Job at TheraEd Staffing Group

 ...We are seeking a fully Remote compassionate and skilled Special Education Teacher to join a dedicated educational team located in Virginia. This is an excellent opportunity to expand your teaching experience while making a lasting impact on students with diverse learning... 

CyberData Technologies

Program Manager - Federal Health IT & Cybersecurity Federal Program Manager | Delivery & Customer Execution Job at CyberData Technologies

 ...Title: Program Manager Federal Health IT & Cybersecurity - Federal Program Manager | Delivery & Customer Execution Location:...  ...certification . Prior experience working with both small business contractors and large federal integrators . Familiarity with HHS,...