About this opportunity
Kailera Therapeutics lists this Associate Director, Bioanalytical Sciences opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
What You’ll Do
The Associate Director, Bioanalytical Sciences at Kailera Therapeutics will report to the Director, Bioanalytical Sciences and will be responsible for designing and executing bioanalytical strategies to support development programs for patients with obesity-related diseases. This role will oversee GLP‑compliant bioanalytical work for non‑clinical and clinical studies. The Associate Director will manage CRO‑outsourced bioanalysis to advance drug candidates through various development stages while partnering with cross‑functional teams to ensure the seamless integration of data into Kailera’s broader development programs.
Required location: Waltham, MA (hub‑based, onsite 3‑4 days per week).
Responsibilities
Lead bioanalytical strategy and execution in clinical and non‑clinical studies
Collaborate with cross‑functional teams to design and implement bioanalytical aspects of clinical development programs
Identify, select, and oversee CROs, ensuring adherence to timelines, budgets, and regulatory requirements
Manage and oversee outsourced bioanalysis of small molecules, peptides, and biomarkers
Direct the development, validation, and implementation of bioanalytical assays
Review validation protocols, test procedures, raw data, and technical reports to ensure scientific rigor and compliance with regulatory guidelines
Provide leadership in ensuring GLP compliance for bioanalysis in both non‑clinical and clinical trials
Author and review bioanalytical sections of regulatory submissions
Represent the bioanalytical function in cross‑functional project teams
Required Qualifications
10+ years of relevant industry experience in bioanalytical sciences with a Bachelor’s degree or 5+ years with an advanced degree
Expertise in regulated bioanalysis and clinical‑stage drug development
In‑depth knowledge of GLP/GCP requirements and industry best practices in bioanalytical laboratories
Proven experience in the regulatory requirements for method development and validation
Strong track record of managing CRO‑outsourced bioanalysis and vendor relationships
Excellent project management skills with the ability to manage multiple priorities effectively
Experience with regulatory interactions is highly desirable
Experience contributing to regulatory filings for biologics and small molecules
Preferred Qualifications
Experience with GLP‑1 receptor agonists or related therapeutic areas
Strong understanding of bioanalytical considerations for incretin‑based therapies
Education
Bachelor’s degree in a relevant scientific discipline required (e.g., bioanalytical chemistry, pharmacology, or related field); PhD preferred
Salary Range: $159,000—$195,000 USD
For Full Time Roles
This range represents the company’s good‑faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year‑end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants—because your well‑being and future matter to us.
Equal Employment Opportunity Information
Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy‑related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
E‑Verify
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.