Associate Director, Clinical Supply Chain

Job description

Job Summary

About IDEAYA Biosciences: IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Our approach integrates expertise in small‑molecule drug discovery, structural biology and bioinformatics with robust internal capabilities in identifying and validating translational biomarkers to develop tailored, potentially first‑in‑class targeted therapies aligned to the genetic drivers of disease. We have built a deep pipeline of product candidates focused on synthetic lethality and antibody‑drug conjugates, or ADCs, for molecularly defined solid tumor indications. Our mission is to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized with the goal of altering the course of disease and improving clinical outcomes for patients with cancer.

When you’re at IDEAYA, you will be in the midst of brilliant minds working on precision medicine therapies to help cancer patients. We are passionate and committed about being on the forefront of oncology medicine, which means we all have a high internal drive that is at the very core of every person at IDEAYA. We are inquisitive, ask deep questions, and are data-driven innovators who like to collaborate and use team work to move science forward. For more information, please see

Location: South San Francisco, CA.

Position Summary

IDEAYA is seeking an Associate Director of Clinical Supply Chain. The role of Associate Director is responsible for providing execution support for all aspects of clinical trial materials (CTM) for all clinical trials of IDEAYA programs. This position will provide support to the leadership of Clinical Supply Chain in the planning, forecasting, material sourcing, packaging and labeling, distribution, return and destruction of IDEAYA investigational drugs. The essential responsibilities of Associate Director include (but not limited to) clinical trial supply management, vendor management, oversight of external partners including depots and Contract packaging Organizations to ensure robust and compliant supply chain for all IDEAYA’s programs and in accordance with applicable laws and regulations. This role requires close coordination and collaboration with stakeholders across multiple functional areas within IDEAYA including CMC, QA, QC, Clin Dev/Clin Ops, Regulatory, and Program Management.

This position is based in our South San Francisco headquarter offices and required to be onsite four days per week per our company policy.

Reporting to: Director, Clinical Supply Chain.

Job Description

What you’ll do:

Clinical Supply Management (General)

Assist with identification and management of external global partners (e.g., depots, couriers, CMOs, IRT vendors) to ensure availability of drug supply at depots/clinical trial sites.

Lead and assist with developing, maintaining, and implementing supply chain policies, procedures, systems and techniques with a focus on continuous improvements.

As requested, assist with the preparation of the departmental budget, collaborate with Finance to address budget and invoice inquiries

Create and/or revise study specific Pharmacy Manuals and supply related training/instructional materials (i.e., Investigator Meeting and Site Initiation Visit slides, Dosing Cards, Diaries, etc.) based on protocol requirements.

Ensure appropriate documentation of IP supply activities is filed for the Trial Master File

Participate in relevant team meetings providing clinical supply status and support

Manage supply planning/demand forecasting to ensure alignment with study activity and timelines

Monitor inventory levels at clinical sites and depots throughout the life of a trial taking preventative actions to avoid potential supply issues; management may be manual or automated depending on study phase and complexity

Establish and document a supply plan for each project as applicable.

Assist with procurement and management of commercially sourced supplies

Follow-up and resolve Temperature Excursions and/or Product Complaints from sites/depots

Ensure expiry extensions are provided to depot/sites as needed to support continued use

Collaborate with study team and vendors to assure proper distribution of clinical supplies to study sites

Manage return and destruction of clinical supplies, with proper documentation of all steps.

Collaborate with the CMC and clinical team in developing CTM supply requirements planning based on forecasts provided by Clinical Operations

Provide and/or support documentation for global shipment of clinical supplies, e.g., proformas and commercial invoice

Support QA with timely review and approval of batch records for packaging and labeling of study drug

Vendor Management/Oversight

Serve as point of contact for third party packaging, labeling, distribution, storage Vendors, and CRO for assigned projects representing Clinical Supply Chain

Serve as the point of contact for study specific IRT URS, UAT and enhancements in support of clinical supply management

Packaging and Labeling

Preparation of label text, coordination of label translations and proofs that align with county specific regulatory requirements

Review of pre and post executed labeling batch records

Liaise with appropriate parties to ensure adequate clinical study supply releases are obtained per applicable regulations (e.g., QP Release, Certificates of Analysis/Compliance, Country specific CTM release)

Coordinate expiry date extensions and re-labeling operations, when applicable

Oversee maintenance of appropriate quantity of retain samples

IRT (Interactive Response Technology) Systems

Work with cross-functional teams to develop study-specific IRT specifications and requirements from a Clinical Supply perspective

Perform user acceptance testing (UAT)

Perform unblinded monitoring of IRT inventory at depots/sites with respect to recruitment

Perform unblinded IRT functionality monitoring to assure resupply generation, etc. occur within defined specifications

Post IRT deployment, manage system updates for supply expiration date extensions, addition of new depot inventory, generation of manual re-supply shipments, evaluation of temperature excursions, etc.

Serve as the point of contact for supply related issues reported by clinical sites and managed within the IRT

Distribution

Oversee and prepare documentation to support import/export of globally transferred CTM as needed

Support movement of CTM from depots to clinical sites regionally from depots

Provide site specific documentation as needed to depots and clinical sites to ensure on time and compliant delivery of CTM to clinical sites

Requirements

BA/BS in Supply Chain, Engineering, or life sciences; certifications such as APICS, CPIM, CIRM, PMP are desirable.

10+ years’ experience in biotech/Pharmaceutical industry with 7+ years’ experience in Supply Chain. Experience with CMC operations is desirable.

Demonstrated ability to establish supply chain strategy from clinical protocol.

Demonstrated knowledge of forecasting and inventory management, pooling supplies, drug product allocation, and IRT drug management modules

Demonstrated experience in management of IRT systems

Demonstrated experience in supporting global oncology trials with globally labelled CTM including packaging and over labeling commercial drug supply for combination trials

Demonstrated skill in successful international shipment, including customs clearance

Proven experience managing clinical drug supply for phase 1-3 global trials, Expanded Access Programs (EAP), and Investigator sponsored trials (IST)

Proven experience working with and managing external packaging and distribution partnersProven experience working with and managing external packaging and distribution partnersLi>"

The successful candidate will be a team player with integrity, a commitment to quality, and the ability to think critically and creatively in a fast‑paced, changing environment

Ability to think strategically to anticipate risk to supply chain and develop mitigation strategy

Having deep understanding of GMP/GDP/GCP, impact of regulatory timing on supply chain, global distribution and logistics

Proficiency in MS Office Suite and IRT. Experience with drug supply forecasting technology is strongly preferred.

Travel required: Yes

Percentage of time in a year: 5-10%

Domestic or International: Domestic

All employees are expected to act with integrity and in full compliance with applicable laws, regulations, and IDEAYA policies, including IDEAYA’s Code of Conduct.

Employees must demonstrate good judgement and ethical behavior in all business activities, maintain patient and product safety as a top priority, and report any suspected violations of law or Company policy through appropriate channels.

Total Rewards

Along with our inspiring mission, and highly collaborative and inclusive environment, IDEAYA offers a competitive total rewards package that reflects our pay‑for‑performance philosophy where employees are eligible to be considered for merit‑based salary increases, company discretionary short‑term incentive plan participation, and company discretionary stock option awards (based on board approval). Our comprehensive benefits package includes, but is not limited to, medical/dental/vision coverage (100% company paid for employees and 90% company paid for dependents), 401k, ESPP, and wellness programs.

The expected salary range for the role of Associate Director, Clinical Supply Chain is $167,000 - $206,000. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the office location where this open position is located, the final candidates’ experience within their profession, experience in the disease areas we are striving to make an impact in as a company, length of time within the industry, educational background, and performance during the interview process.

The Company complies with all laws respecting equal employment opportunities and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state, and local law.

IDEAYA is an equal opportunity employer. In accordance with applicable law, IDEAYA does not discriminate in hiring or otherwise in employment based on race, color, religion, sex, national origin, age, marital or veteran status, disability, sexual orientation, or any other legally protected status. EOE/AA/Vets.

We are committed to providing reasonable accommodations to qualified individuals with disabilities. If you need assistance or an accommodation due to a disability, please get in touch with us at

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Worksite address

south san francisco, CA, 94083, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.