Associate Director, Marketing

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. C4Ts degrader medicines are designed to harness the bodys natural protein recycling system to rapidly degrade disease-causing proteins offering the potential to overcome drug resistance drug undruggable targets and improve patient outcomes. For more information please visit .

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 at C4T. Your 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 C4Ts 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.

Competitive Intelligence

• 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 Cemsidomides development and messaging.

Congress Booth Presence

• Own C4Ts 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 Bachelors 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 malignancies experience strong preferred including multiple myeloma experience ideally on a launch or pre-launch team.
• Experience at a small or emerging biotech building processes from scratch.
• Familiarity with the healthcare professional community

Compensation

The base pay range for this position at commencement of employment is expected to be between $199104.00 $219500.00 annually; however base pay offered may vary depending on multiple individualized factors including job-related knowledge skills and experience.

C4 Therapeutics is an Equal Opportunity Employer.

Required Experience:

Director