Program Manager, CMC

Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow‑on product candidate, OP-3136, is a potent KAT6 inhibitor with best‑in‑class potential. About the Role: Program Manager, CMC As the Program Manager, CMC reporting to the Director, CMC Program Management, you will lead integrated CMC program planning and execution across clinical development stages. You will translate CMC strategy into actionable, integrated plans that enable timely clinical and regulatory progress. This role is highly cross‑functional and requires close collaboration with Technical Operations (CMC technical leads), Quality, Regulatory, Supply Chain, Finance and external partners. You will serve as an operational leader – driving accountability, facilitating alignment, managing risk, and helping teams navigate challenges effectively. This role can be based out of our San Francisco, CA or Boston, MA offices and will require 10% travel. Responsibilities Lead integrated CMC planning across Drug Substance (DS), Drug Product (DP), Analytical (AC), Quality (QA), Regulatory (RA), and Supply Chain (SC), partnering with Director‑ and Senior Director‑level functional leaders to define deliverables, timelines, and priorities aligned to clinical and regulatory goals. Build and maintain integrated project timelines in Smartsheet (or similar tools), ensuring dependencies, critical path activities, and milestones are clearly defined and tracked. Identify program risks, drive mitigation planning with functional leads, and escalate issues as needed to maintain timelines. Facilitate CMC sub‑team meetings, document decisions and action items, and ensure follow‑through across internal teams and external partners. Prepare leadership‑ready status updates and presentations, track key program metrics, and maintain clear documentation of plans, risks, and decisions. Support regulatory submission readiness by aligning CMC deliverables, documentation, and cross‑functional inputs to filing timelines. Partner with Technical Operations and CDMOs to drive coordinated execution and proactively identify risks to supply or compliance. Strengthen CMC program management practices, tools, and planning processes to support scalable, efficient execution. Provide program‑level budget visibility and tracking in collaboration with functional leads and Finance. Contribute to a collaborative, accountable, and team‑oriented culture within CMC and across Olema. Ideal Candidate Profile Knowledge Bachelor's degree required, Life Sciences or related disciplines preferred. Proficiency in Microsoft Office Suite (PowerPoint, Excel, Outlook), Smartsheet (or equivalent PM tools), and collaboration platforms (e.g., MS Teams, SharePoint). Knowledge of CMC development processes across clinical stages. Familiarity with regulatory submission timelines and CMC documentation requirements preferred. Experience Minimum 5+ years of experience in life sciences program management and/or drug development operations with a bachelor's degree, or 3+ years with a master's degree. Experience driving CMC execution in early clinical‑stage development (Phase 1–2), with exposure to Phase 3 readiness considered a plus. Working cross‑functionally within drug development teams (Drug Substance, Drug Product, Analytical, Quality, Regulatory Affairs, Supply chain). Demonstrated experience building and managing integrated project plans, identifying critical path activities, and proactively managing risks and dependencies. Collaborating and interacting with external vendors/CDMOs. Experience preparing materials for team or leadership meetings. Attributes Highly organized with strong attention to detail and follow‑through. Energetic, proactive, and action‑oriented — a true “go‑getter.” Friendly and approachable with a collaborative mindset. Strong communicator who can tailor messaging to diverse audiences. Skilled at bridging functions and building strong working relationships. Comfortable navigating a fast‑paced, evolving environment. Solutions‑oriented with sound judgment and appropriate escalation. Strong team player who thrives in highly collaborative settings. The base pay range for this position is expected to be $150,000-$170,00 annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits. Important Information We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated. We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long‑term careers. A Summary of Benefits is available for all applicants. Please note: Olema doesn’t accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you. Fraud Alert: We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema’s official email addresses end in @olema.com. Our official corporate website is olema.com; our careers page is #J-18808-Ljbffr Olema Oncology