Sr. Manager GRA Audits, Inspections and Compliance - Pipeline

Takeda Pharmaceutical Co.; Kendall Square (MA); Presencial; USD 137.000 - 215.000; Jornada completa

Descripción de la vacante

Takeda Cambridge, MA is seeking a Senior Manager, GRA Audits, Inspections and Compliance to lead global management of GCP audits and inspections within Regulatory Affairs. You will ensure readiness, provide live support during audits, manage post-audit follow-up and drive process improvements across Global Regulatory Affairs.

The role requires a Bachelor’s in science or business, 5+ years in pharma with 3+ in regulatory/compliance, experience with Veeva (RIM and Clinical), strong communication,

Formación

• Bachelor's degree in a science- or business-related field.
• Minimum of 5 years in pharma, including at least 3 years in clinical trial management, Regulatory Affairs, Quality Assurance or Compliance.
• Deep knowledge of global regulatory requirements for clinical trials across major markets.
• Experience using the Veeva platform, including RIM and Clinical.

Responsabilidades

• Manage, coordinate and follow up on GCP audits and inspections globally.
• Support audit/readiness and provide live support during audits and inspections.
• Lead post-audit and post-inspection follow-up activities.
• Collaborate with GCP Compliance, GCP Excellence and Clinical Program Quality teams.
• Align regulatory initiatives with stakeholders and drive process improvements.
• Build relationships to implement global regulatory processes and systems.

Conocimientos

GCP audits

Regulatory affairs

Quality Assurance

Cross-functional collaboration

Veeva platform (RIM/Clinical)

Communication skills

Educación

Bachelor's degree in science or business

Herramientas

Veeva RIM

Veeva Clinical

Descripción del empleo

About the role

The Senior Manager, GRA Audits, Inspections and Compliance (GRAIC) - Pipeline provides expertise and support for the global management, coordination and follow-up of GCP audits and inspections related to Regulatory Affairs processes. This role helps ensure inspection readiness, provides live support during audits and inspections, manages post-audit and post-inspection follow-up, and drives continuous improvement across Global Regulatory Affairs.

How you will contribute

• Manage, coordinate and follow up on GCP audits and inspections related to Regulatory Affairs processes globally, helping ensure readiness and compliance.
• Partner closely with International Clinical Trial Regulatory Leads and Global Regulatory Leads to support audit and inspection readiness.
• Act as a liaison among GCP Compliance, GCP Excellence and Clinical Program Quality teams.
• Monitor and support global regulatory compliance performance for Global Regulatory Leads across therapeutic areas, including Neuroscience, Oncology, Gastrointestinal, MPD and International Clinical Trial Regulatory Leads.
• Align Global Regulatory Affairs initiatives and implementation strategies with relevant stakeholders across the organization.
• Build collaborative relationships with Global Regulatory Leads and International Clinical Trial Regulatory Leads to develop and implement global regulatory processes and systems.
• Lead and contribute to efforts that simplify and optimize business processes and platforms, including opportunities to automate and harmonize processes.

Skills and Qualifications

• Bachelor's degree in a science- or business-related field.
• Minimum of 5 years of experience in the pharmaceutical industry, including at least 3 years in clinical trial management, Regulatory Affairs, Quality Assurance and/or Compliance.
• Deep knowledge of global regulations related to clinical trials across major markets, with practical experience working cross-functionally and across regions in multicultural, matrixed organizations.
• Experience using the Veeva platform, including Veeva RIM and Veeva Clinical.
• Clear and effective communication skills, with the ability to synthesize and communicate complex issues to diverse internal and external stakeholders, both verbally and in writing.
• Ability to proactively identify and anticipate risks of non-compliance in a complex environment.
• Ability to manage conflict tactfully and diplomatically while seeking effective solutions for all parties.
• Ability to manage multiple priorities within time and resource constraints.
• Critical-thinking skills and the ability to analyze complex or ambiguous information, assess its impact on products and processes, and communicate findings effectively.

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.

Location: Cambridge, MA 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.

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

Cambridge, MA

Worker Type

Employee

Worker Sub-Type

Regular Time

Time Type

Full time

Job Exempt

Yes

Legal Note

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.

About Takeda

Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own.

Takeda is an equal opportunity employer.