Senior Manager, GCP QA

Shionogi Inc. (U.S.); Florham Park (NJ); On-site; USD 135,000 - 165,000; Full time

Job summary

Shionogi Inc. (U.S.) is looking for an experienced Senior Manager, GCP QA to ensure quality oversight of clinical studies while maintaining ICH GCP and FDA compliance. This pivotal role involves collaborating with clinical study teams, conducting audits, and providing GCP guidance.

The ideal candidate should possess a BA/BS in life sciences, at least 5 years of relevant experience, and a strong understanding of GCP regulations. The role requires travel up to 25% and an office presence at least 50% of the time.

The base salary range for this position is $135,000 - $165,000.

Qualifications

• Minimum of 5 years of experience in a GCP QA/quality/compliance role.
• Working knowledge of GCP regulations including ICH, FDA, EMA.
• Experience in performing GCP-related audits.

Responsibilities

• Provide quality oversight and GCP guidance to clinical teams.
• Evaluate clinical trial documentation for compliance.
• Perform GCP audits and manage the audit process.

Skills

Attention to detail

Communication skills

Critical thinking

Problem-solving abilities

Education

BA/BS in life sciences or related field

Job description

We are seeking an experienced Senior Manager, GCP QA to join our team. This role is crucial for ensuring quality oversight of clinical studies and vendor programs, maintaining compliance with ICH GCP and FDA regulatory requirements, and upholding our high standards for data integrity. The ideal candidate will provide advisory and collaborate with clinical study teams and internal departments to assess and mitigate risks associated with vendors.

Responsibilities

• Provide quality oversight and GCP guidance to clinical study teams and CROs/vendors to ensure compliance with ICH GCP and FDA regulatory requirements, as well as Shionogi standards.
• Ensure clinical trials adhere to GCP principles, producing high-quality and reliable data.
• Evaluate clinical trial documentation, processes, and study plans to ensure alignment with Shionogi’s expectations and regulatory requirements.
• Interpret and evaluate clinical and regulatory compliance requirements in coordination with the GCP QA team to meet company obligations.
• Collaborate with clinical study teams to provide vendor quality oversight, identify risks, and propose remediation actions. Conduct CRO or vendor audits or assessments.
• Develop, as needed, and ensure the GCP audit plan(s) is(are) executed for assigned clinical studies as part of quality oversight. Conduct investigator site audits or TMF audits.
• Work with internal cross-functional teams to assess risks associated with vendors and implement risk mitigation strategies to ensure product quality, study compliance, data integrity, and patient safety.

General Quality And Regulatory Compliance

• Maintain up-to-date knowledge of applicable regulations, industry standards, and Shionogi GCP standards and their interpretations.
• Provide guidance on quality and compliance issues, ensuring adherence to applicable regulations, guidelines, and company policies.
• Evaluate the effectiveness of CAPAs and follow up on audit findings to ensure timely resolution.

Audit Support

• Perform GCP audits (e.g., CRO, vendor, investigator site, TMF, internal process) and manage the GCP audit process for self-performed audits and outsourced audits.
• Support GCP regulatory inspections and manage assigned CAPAs identified during inspections.
• Other duties as assigned.

Minimum Job Requirements

Qualifications

• BA/BS in life sciences, a scientific, technical discipline, or a related field.
• Minimum of 5 years of experience in a GCP QA/quality/compliance role supporting clinical study teams.
• Working knowledge of GCP regulations and guidelines, including ICH, FDA, EMA, and PMDA requirements.
• Experience in performing GCP-related audits.

Competencies

• Strong attention to detail, team player, agile, excellent communication skills, strong critical thinking skills, and effective problem-solving abilities.
• Experience with various types of clinical trials and familiarity with additional regulatory environments.
• Capable of operating in an ambiguous environment.
• Capable of operating independently with a leveled understanding of decision making.

Other Requirements

• Ability and willingness to travel up to 25% of the year both domestically and internationally.
• Must live a commutable distance to our US Corporate Headquarters in Florham Park, NJ. Office presence required at least 50% of the time per month.

Additional Information

The base salary range for this full-time position is $135,000 - $165,000. Individual pay is determined by several factors, which include but are not limited to: job-related skills, experience, and relevant education or training. The range does not include the comprehensive benefits, bonus, long-term incentive, applicable allowances, or any additional compensation that may be associated with this role.

EEO

Shionogi Inc. is an equal opportunity employer supporting individuals with disabilities and veterans. All qualified applicants will receive equal consideration for employment opportunities based on valid job requirements without regard to race, color, religion, sex (including pregnancy), marital status, national origin, age, ancestry, citizenship, disability, genetic information, status as a disabled veteran, a recently separated veteran, Active Duty Wartime or Campaign Badge Veterans, and Armed Forces Service Medal Veterans, or any other characteristic protected by applicable law. It is the policy of Shionogi Inc. to undertake affirmative action for protected veterans and individuals with disabilities in compliance with all federal, state, and local requirements to recruit a diverse pool of protected veteran and individuals with disabilities applicants and to ensure that our employment practices are, in fact, non-discriminatory.

If you are qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request accommodations by calling 973-307-3550 or by sending an email to [e-mail].