Senior Principal Pharmacovigilance Scientist

Takeda Pharmaceutical Co.; Agawam (MA); Hybrid; USD 137,000 - 215,000; Full time

Job summary

Takeda Pharmaceutical Co. seeks a Pharmacovigilance Scientist, Senior Scientist to ensure regulatory compliance and safety of Takeda's products.

You will manage large projects, develop innovative solutions, and lead teams, contributing to pharmacovigilance strategies and patient safety. This role involves leading risk management, safety reporting, signal detection, and stakeholder engagement with regulators.

Qualifications

• Applies comprehensive risk management strategies in complex situations.
• Expert in pharmacovigilance with ability to coach others.
• Ensures regulatory compliance with deep understanding of safety regulations.

Responsibilities

• Manage large pharmacovigilance projects with limited oversight.
• Develop and implement risk management strategies for complex situations.
• Lead preparation and review of detailed safety reports.
• Conduct signal detection and safety assessments independently.
• Engage with stakeholders and regulatory authorities, providing authoritative advice.
• Lead and mentor junior staff, fostering a collaborative environment.
• Deliver training on pharmacovigilance practices to enhance team capabilities.

Skills

risk management

regulatory compliance

safety reporting

signal detection

clinical development

stakeholder management

mentoring

Job description

Job Description

About the role: The Pharmacovigilance Scientist, Senior Scientist ensures regulatory compliance and safety of Takeda's products by managing large projects, developing innovative solutions, and leading teams. This role contributes to the development and execution of pharmacovigilance strategies, ensuring patient safety and regulatory adherence.

How you will contribute

• Manage large pharmacovigilance projects or processes with limited oversight
• Develop and implement risk management strategies for complex situations
• Lead the preparation and review of detailed safety reports
• Conduct signal detection and safety assessments independently
• Engage with stakeholders and regulatory authorities, providing authoritative advice
• Lead and mentor junior staff, fostering a collaborative environment
• Deliver training on pharmacovigilance practices to enhance team capabilities

Skills and qualifications

• Applies comprehensive risk management strategies in complex situations, capable of advising others
• Recognized as an expert in pharmacovigilance, able to develop strategic safety initiatives and coach others
• Ensures regulatory compliance with a deep understanding of safety regulations and guidelines
• Proficient in safety reporting and able to lead the preparation of detailed reports
• Conducts signal detection and safety assessments independently, providing critical analysis
• Experienced in clinical development, contributing to the strategic planning and execution of clinical trials
• Engages effectively with stakeholders and regulatory authorities, providing authoritative advice
• Leads teams effectively, fostering a collaborative environment and mentoring junior staff
• Delivers training on pharmacovigilance practices, enhancing team capabilities
• Communicates complex safety data clearly and effectively to various audiences
• Analyzes safety data meticulously to make informed decisions
• Demonstrates strong decision-making skills in high-stake environments

As an expert professional within the organization, you develop innovative solutions to complex problems aligned with organizational objectives. Your work involves addressing intricate issues, requiring in-depth analysis and judgment. You also engage with key contacts outside your expertise area and contribute to the development of new concepts and standards. Operating with considerable autonomy, you serve as a consultant to management and an external spokesperson on major matters, often working independently and leading function teams or projects. Additionally, you play a role in training and mentoring junior staff.

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:

$137,000.00 - $215,270.00

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.

For information about our benefits, please click here.

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

YesIt 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