Sr. Associate, Clinical Supplies Planning and Logistics

About Us

Structure Therapeutics develops life-changing medicines for patients using advanced structure-based and computational drug discovery technology. The company's platform combines the latest advancements in molecular interactions visualization, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical-stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and capitalizing on the strengths of each geographic location.

Position Summary

Structure is seeking a talented, independent, and highly motivated entry-level Clinical Supplies Professional with experience in relevant fields. They will be involved in typical clinical supply activities including forecasting Investigational Product (IP) supply requirements, packaging, labeling, and inventory management, and managing distribution through 3rd party vendors, for multiple clinical trials.

Job Responsibilities

• Participates in clinical supply and logistics activities, including but not limited to demand forecasting and supply planning, label text generation and approval, packaging and labeling operations at clinical supply vendors, batch record review, distribution management, temperature excursion, expiry extension, drug return and destruction records, and inventory management.
• Manages IP vendors: participates in packaging planning, label proof review, batch record review, weekly meetings, etc.
• Collaborate with external partners (CMOs, CROs, shipping and IRT vendors, study sites) and study team members to ensure successful execution of clinical trials.
• Collaborate with Clinical Operations and Regulatory Affairs to provide packaging and labeling information, including labeling and packaging design in compliance with relevant SOPs, policies, and regulations.
• Works closely with QA to ensure compliance with IP documentation, procedures, Lot numbers, managing expiration dates, and coordinating release schedules.
• Tracks GCP adherence at sites.
• Supports inspection team in preparation for and during regulatory agency inspection.
• Ensures appropriate documentation of IP supply activities is provided to clinical trial teams for the Trial Master File.
• Supports the review of IP-related study documents (e.g., pharmacy manual, IP section of protocol) and training materials for clinical study teams and investigational site use as needed.
• Provides input to and review of drug kit randomization specifications and master kit lists.

Education/Experience

• Bachelor's degree (BA/BS) required, scientific discipline, or Supply Chain management preferred.
• 3+ years of relevant experience in one or more of the following areas: Clinical Supplies, QA, manufacturing, process development, materials management, and/or analytical development in a GxP environment in the biotechnology/pharmaceutical industry.
• Or supply chain management or packaging design in any industry with demonstrable knowledge of scientific principles.
• Experience in global logistics a plus.
• Knowledge of cGMP, GCP, GDP, and/or GLP strongly preferred.
• Experience in forecasting, labeling, and/or distribution management.
• 2+ years using Microsoft Office applications, including Excel, Smartsheets a plus.

Qualitative Requirements

• Organizational skills.
• Result-driven.
• Strategic agility.
• Resilience and flexibility dealing with ambiguity.
• The ability to prioritize and handle multiple activities on a daily basis while being flexible and responsive to frequently shifting priorities.
• Demonstrated ability to integrate into a partially remote team environment (US, EU, LATAM, APAC) with a positive attitude.
• Action-oriented with excellent problem-solving skills.
• Strong sense of integrity, ethics, and honesty.

Pay & Benefits

The anticipated base pay range for this role is $109,000 - $135,000. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience. At Structure, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Structure Therapeutics also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, unlimited PTO, and a number of paid holidays including winter shutdown.

Notice to Recruiters/Staffing Agencies

Recruiters and staffing agencies should not contact Structure Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees. We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file. Structure Therapeutics’ receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Structure Therapeutics and such organization and will be considered unsolicited and Structure Therapeutics will not be responsible for related fees.

Fraud Alert

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