Associate Director, Marketing

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Marketing Full Time Management Watertown, MA, US

2 days ago Requisition

Salary Range: $ To $ Annually

About C4 Therapeutics:

C4 Therapeutics (C4T) (Nasdaq: CCCC) is a clinical-stage biopharmaceutical company dedicated to delivering on the promise of targeted protein degradation science to create a new generation of medicines that transforms patients' lives. C4T is progressing targeted oncology programs through clinical studies and leveraging its TORPEDO platform to efficiently design and optimize small-molecule medicines to address difficult-to-treat diseases. C4T's degrader medicines are designed to harness the body's natural protein recycling system to rapidly degrade disease-causing proteins, offering the potential to overcome drug resistance, drug undruggable targets and improve patient outcomes.

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Job Summary

The Associate Director, Marketing will own the pre-launch brand foundation for cemsidomide: market definition, positioning, and early launch planning in multiple myeloma. You will work hands-on, translating clinical data into a clear strategic story and partnering closely with Medical Affairs, Clinical Development, Market Access, and Corporate Communications. As cemsidomide is investigational, all external activity will be non-promotional and compliant with pre-approval guidelines.

This is an exciting opportunity for someone equally comfortable designing a marketing campaign and running a physician advisory board to get in on the ground level of our commercial build out r skills and passion for this space will allow you to have a front row seat to see what it looks like to build out a commercial function at a small life sciences company as one of our first dedicated commercial hires.

Your Role

Messaging Development

• Lead development of disease-state and messaging for multiple myeloma, translating clinical data into clear, compliant narratives.
• Run message testing with hematologist-oncologists, community oncologists, and other customers; refine messages as data mature.
• Build and maintain the core messaging platform and ensure consistent use across venues and audiences.
• Take materials through Medical/Legal/Regulatory review with a clear grasp of pre-approval compliance.

Agency of Record (AOR) Selection and Onboarding

• Lead the search for C4T's first marketing AOR: define requirements, build the RFP, run pitches, and recommend a partner.
• Onboard the selected agency: brief them on the disease area, science, and compliance expectations; set up ways of working, review cadence, and scopes of work.
• Manage the agency day to day, including budgets, timelines, and quality of deliverables.

Advisory Boards

• Plan and run advisory boards with KOLs and community physicians, in partnership with Medical Affairs, to gather customer insights.
• Set objectives, design discussion guides, select participants, and manage logistics with vendors.
• Synthesize findings into clear recommendations and share them with cross-functional and senior leadership.
• Track the MM landscape, including next-generation IKZF1/3 degraders, BCMA- and GPRC5D-directed bispecifics, CAR-T, and anti-CD38 regimens.
• Lead congress coverage and competitive readouts at key meetings.
• Deliver regular competitive intelligence updates and assess implications for Cemsidomide's development and messaging.

Congress Booth Presence

• Own C4T's corporate and disease-awareness booth presence at major hematology and oncology congresses.
• Lead booth concept, design, and content with the AOR, medical affairs and exhibit vendors, ensuring all content is non-promotional and approved.
• Manage booth logistics, staffing, budget, and post-congress performance reviews.

Your Background

Required:

• A Bachelor's Degree in life sciences, business, or a related field with a minimum of eight years in the pharmaceutical or biotechnology space, including at least five years in product or brand marketing, including oncology marketing experience.
• Hands-on experience turning corporate and departmental strategy into marketing execution with a strong sense of independence.
• Working knowledge of pre-approval compliance and the Medical/Legal/Regulatory review process.
• Ability to read and communicate clinical trial data with accuracy and confidence.

Preferred

• MBA or advanced scientific degree (PharmD, PhD, MS).
• Hematologic…