Sr. Manager, Bioanalysis

Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in four disease areas: bone and mineral; intractable hematologic; hematology oncology; and rare disease.  A Japan-based company, our goal is to translate science into smiles by delivering therapies where no adequate treatments currently exist, working from drug discovery to product development and commercialization. In North America, we are headquartered in Princeton, NJ, with offices in California, North Carolina, and Mississauga, Ontario.

Summary:

The Senior Manager, Bioanalysis plays a key role in advancing Kyowa Kirin’s pipeline through providing bioanalytical support and strategy to cross-functional and cross-regional teams for early-phase and late-phase clinical studies, as a bioanalytical SME and a member of Bioanalysis sub-team of global Clinical Pharmacology department. This position involves managing regulated bioanalysis conducted at bioanalytical CROs throughout the assay lifecycle (assay validation through all phases of clinical sample analysis). The role integrates a deep understanding of regulated bioanalysis and effective communication across global cross-functional teams to support program strategy and execution. 

Essential Functions:

•    Managing PK and immunogenicity bioanalysis conducted at CROs including on-site CRO visits and assay troubleshooting with support from internal SMEs.
•    Providing bioanalytical guidance on PK and immunogenicity required for clinical projects to cross-functional global clinical study teams, including advising on bioanalytical sample collection and processing, and storage, and data transfer procedures.
•    Reviewing clinical study protocols and providing bioanalytical summaries and reports for clinical pharmacology reports and CSRs. 
•    Developing summary documents for regulatory submission and participating in strategic communication with regulatory agencies. 
•    Extensive collaboration with counterparts in Japan on activities/initiatives for bioanalytical method development/transfer, CRO qualification/ selection/visits, and process improvements, including creation of work instructions (WIs) and Standard Operation Procedures (SOPs) and co-leading task forces.
•    Ensuring full compliance with current global and local bioanalytical guidance and GxPs. 
•    Simultaneously completing tasks on multiple projects including method validation and sample analysis activities, with support from internal team members.

Requirements:

Education
Bachelor’s degree in life sciences, healthcare, or closely related discipline is required. An advanced degree (MS or PhD) is highly desirable.

Experience
•    Minimum of five (5) years of pharmaceutical industry experience (Sponsor and/or CRO) in the bioanalysis of large and small molecule therapeutics.
•    Three (3) or more years of hands-on experience at a bioanalytical CRO or in conducting vendor oversight to support clinical development programs across all phases; experience with early-phase programs is strongly preferred.
•    Proven experience in preparing strategic regulatory communications and developing reports and summary documents for regulatory submissions.
•    Demonstrated ability to manage expedited sample analysis timelines while ensuring high-quality data delivery.
•    Experience in authoring and reviewing Work Instructions, Manuals, and/or Standard Operating Procedures (SOPs).

• Technical Skills
•    Strong familiarity with bioanalytical assay methodology including ligand-binding and cell-based assays, LCMS/MS, and novel technologies. 
•    Strong analytical skills to resolve technical issues. 
•    Ability to effectively use tables, figures, and listings for data review (adequacy of bioanalysis) and cleaning (no missing samples).
•    Advanced knowledge of guidance documents issued by ICH and local regulatory agencies such as FDA, EMA, PMDA, Health Canada.
•    Familiarity with critical reagents lifecycle management. 
•    Basic proficiency in MS Office Suite
• Working Conditions:
• Requires up to 10% domestic and international travel

The anticipated salary for this position will be $155,000 to $170,000.  The actual salary offered for this role at commencement of employment may vary based on several factors including but not limited to relevant experience, skill set, qualifications, education (including applicable licenses and certifications, job-based knowledge, location, and other business and organizational needs.

The listed salary is just one component of the overall compensation package. At Kyowa Kirin North America we provide a comprehensive range of benefits including:

• 401K with company match
• Discretionary Profit Share
• Annual Bonus Program (Sales Bonus for Sales Jobs)
• Generous PTO and Holiday Schedule which includes Summer and Winter Shut-Downs, Sick Days and, Volunteer Days
• Healthcare Benefits (Medical, Dental, Prescription Drugs and Vision)
• HSA & FSA Programs
• Well-Being and Work/Life Programs
• Life & Disability Insurance
• Concierge Services
• Long Term Incentive Program (subject to job level and performance)
• Pet Insurance
• Tuition Assistance
• Employee Referral Awards

The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.

KKNA and all of its employees have an obligation to act in accordance with the law and with integrity in all our operations and interactions

It is the policy of Kyowa Kirin North America, Inc. to provide equal employment opportunity to all qualified persons without regard to race, religion, creed, color, pregnancy, sex, age, national origin, disability, genetic trait or predisposition, veteran status, marital status, sexual orientation or affection preference or citizenship status or any other category protected by law.

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Your personal data will be retained by Controller as long as Controller determines it is necessary to evaluate your application for employment.  Under the GDPR, if you are located in the European Union, you have the right to request access to your personal data, to request that your personal data be rectified or erased, and to request that processing of your personal data be restricted. You also have the right to data portability, and to lodge a complaint with an EU supervisory authority. If you have any questions about our use of your data, you may contact us by email at usprivacyoffice@kyowakirin.com.

Recruitment & Staffing Agencies

Kyowa Kirin does not accept agency resumes unless contacted directly by internal Kyowa Kirin Talent Acquisition. Please do not forward resumes to Kyowa Kirin employees or any other company location; Kyowa Kirin is not responsible for any fees related to unsolicited resumes.

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