Senior Manager, Clinical Quality Assurance

Deciphera Pharmaceuticals; Waltham (MA); On-site; USD 138,000 - 190,000; Full time

Benefits offered by this job

Competitive salary and annual bonus

Comprehensive benefits package

Parental leave and family planning benefits

Opportunities for personal growth

Job summary

Deciphera Pharmaceuticals in Waltham, MA, is seeking a Senior Manager, Clinical Quality Assurance to oversee GCP activities for clinical trials. This role involves ensuring compliance with regulatory standards and working closely with clinical operations.

The ideal candidate will have over 8 years of pharmaceutical experience, a Bachelor's degree, and strong abilities in project management and compliance oversight. Deciphera offers competitive compensation and robust benefits.

Qualifications

• Must have 8+ years of direct GCP experience.
• Strong understanding of ICH E6R3.
• Ability to handle multiple projects under pressure.

Responsibilities

• Develop and maintain Clinical QA SOPs.
• Conduct internal and external audits.
• Assist with inspection readiness.

Skills

GCP pharmaceutical/biotechnology experience

Interpersonal skills

Project management abilities

Knowledge of GCP, GLP and ICH requirements

Education

Bachelor's degree or equivalent

Job description

Job Description

The Senior Manager, Clinical Quality Assurance is responsible for the development, maintenance and oversight of GCP activities related to the Clinical Trial activities sponsored by Deciphera. The primary responsibilities are to ensure both quality and compliance of Deciphera sponsored clinical trials with respect to Standard Operating Procedures, applicable regulatory requirements (US FDA, ICH, and country specific), along with current industry standards and practices.

Key Responsibilities

Clinical Quality Support 50%

• Draft, review or revise Clinical QA SOPs to assess consistency and compliance with regulatory requirements/internal standards
• Attend cross-functional team meetings and provide guidance to clinical operations staff based on interpretation of current regulations to ensure best practices including risk-based management
• Work closely with Clinical Operations to ensure/coordinate appropriate and complete resolution of findings/non‑compliant issues, quality investigations, etc. in a timely manner, including approval of corrective action and preventative action (CAPA) plans, as necessary
• Provide Quality Control (QC) review of clinical protocols, amendments, Informed Consent Forms, Clinical Study Reports and other clinical trial related documents
• Assist and advise with training QA and clinical staff as necessary for GCP
• Identify potential systemic gaps and coordinate with the appropriate stakeholder to ensure timely remediation
• As appropriate, elevate issues of critical non‑compliance and/or lack of urgency in remediation to senior management via the Quality Board
• Perform program specific root cause analysis of compliance issues and provide the appropriate metrics for tracking and trending for the overall QA reporting requirements to functional and senior management

Audit Planning and Oversight 40%

• Conduct and/or assist in internal audits (systems, processes, vendors, computer system validation)
• Interact with contract auditors in the scheduling process, kick‑off meetings with auditors and internal groups, assist in the drafting of audit plans, confirmation letters and agendas, etc.
• Identify the need for, conduct and/or assist in external audits (includes, but is not limited to, investigator sites, central IRBs, CROs and clinical labs)
• Oversee the audit response process for the Investigator Site and Contract Research Organization (CRO) audits/inspections and ensure acceptability of actions to address findings through the CAPA process

Inspections 10%

• Assist with inspection readiness, and regulatory inspections as needed

Qualifications

Other duties and responsibilities as assigned.

• 8+ years of direct GCP pharmaceutical/biotechnology experience with Bachelors degree or equivalent
• Solid understanding and application of GCP, GLP and ICH requirements, especially ICH E6R3
• A well organized, self‑motivated and independent work style with the ability to initiate and follow through on assignments
• Excellent interpersonal skills with knowledge of basic negotiation, influencing and conflict management to assure effective interactions within and across departments
• The ability to simultaneously handle multiple project issues while dealing with time demands, incomplete information, or unexpected events
• Broad experience in product development, clinical operations, regulatory compliance and GCP auditing
• Willingness to travel up to 25% both domestic and international

Additional Information

Deciphera is committed to fair and equitable compensation practices. The base salary pay range for this role is $138,000 – $190,000. Actual compensation packages will depend on various factors, including, but not limited to depth of experience, education, skillset, overall performance and/or location.

Deciphera believes in providing a competitive compensation and benefits package to all employees. Our base salary is just one component of Deciphera’s competitive total rewards strategy that also includes annual performance bonus, a long‑term incentive plan, full range of benefits and other incentive compensation plans (if applicable).

Benefits

• Competitive salary and annual bonus.
• Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match, and more.
• Generous parental leave and family planning benefits.
• Outstanding culture and opportunities for personal and professional growth.

Apply Now

Join us in our mission to improve the lives of people with cancer. Apply today to become a part of our dynamic team!

EQUAL EMPLOYMENT OPPORTUNITY INFORMATION

Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements, we invite you to complete the confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. We are committed to make all hiring decisions and other employment decisions on a non‑discriminatory basis.