Olema Oncology

Program Manager, CMC

Olema Oncology$150K — $170K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences or related field required.
  • Proficiency in Microsoft Office Suite, Smartsheet or equivalent PM tools.
  • Knowledge of CMC development processes across clinical stages.
  • Familiarity with regulatory submission requirements preferred.
  • Minimum 5+ years in life sciences program management or drug development.

Responsibilities

  • Lead integrated CMC planning across various functions and clinical stages.
  • Build and maintain project timelines in Smartsheet, ensuring clarity on deliverables.
  • Identify and mitigate program risks, escalating issues when necessary.
  • Facilitate CMC sub-team meetings, ensuring all action items are documented and tracked.
  • Prepare leadership-ready updates and maintain clear documentation of project statuses.

Benefits

  • Competitive compensation package including equity and bonus.
  • Open and flexible work environment.
  • Opportunities for long-term career development.
  • Collaborative and team-oriented culture.
  • Commitment to diversity and equal opportunity for all employees.
Full Job Description
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.

Your work will primarily encompass:
  • 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 >>>

A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role.

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.

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About Olema Oncology

Olema Oncology is a clinical-stage biopharmaceutical company that develops targeted therapies for women's cancers. The company's lead product candidate, OP-1250, is a small molecule inhibitor of the estrogen receptor (ER) that is being developed for the treatment of breast cancer. OP-1250 has demonstrated preclinical activity in ER-positive breast cancer models and is currently being evaluated in a Phase 1/2 clinical trial. Olema Oncology is also developing a pipeline of other small molecule inhibitors of the ER and other targets for the treatment of breast and gynecologic cancers.
Learn more about Olema Oncology
Size
50 employees
Industry
Founded
2013
NASDAQ

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