Full-Time

Manager – CMC Project Management

Crescent Biopharma

Crescent Biopharma

51-200 employees

Clinical-stage biotech developing solid-tumor therapies

Compensation Overview

$140k - $180k/yr

+ Performance bonus + Equity

Waltham, MA, USA

In Person

Bachelor's

Category
Project & Program Management (1)
Required Skills
Supply Chain Management
Forecasting
Quality Assurance (QA)
Risk Management

Get referred to Crescent Biopharma

See people who can refer or advise you

Requirements
  • A bachelor's degree in a scientific, engineering, or related discipline is required.
  • Five to eight years of biotech or pharmaceutical industry experience.
  • Experience in CMC, Technical Operations, Project Management, Manufacturing, Supply Chain, or related functions.
  • Familiarity with good manufacturing practice (GMP) manufacturing and external partner management.
  • Strong project management and organizational skills.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Experience with project planning and tracking tools.
  • Ability to identify risks and drive issue resolution.
  • Experience in the oncology space.
  • Detail-oriented with strong follow-through and accountability.
Responsibilities
  • Lead cross-functional CMC project management for clinical-stage development programs by developing and maintaining integrated project plans, timelines, critical path activities, milestones, risks, and decision logs.
  • Drive project execution by facilitating cross-functional meetings, tracking actions and decisions, proactively identifying risks and dependencies, and escalating issues to ensure program objectives are achieved.
  • Coordinate activities across Drug Substance, Drug Product, Analytical Development, Quality Control, Quality Assurance, Supply Chain, Regulatory CMC, and other Technical Operations functions to align priorities and deliverables.
  • Partner with contract development and manufacturing organizations, contract research organizations, testing laboratories, and other external vendors to monitor deliverables, manufacturing activities, timelines, and issue resolution.
  • Coordinate planning and execution of CMC regulatory submissions, including Investigational New Drug applications, Investigational Medicinal Product Dossiers, amendments, and health authority responses, ensuring cross-functional deliverables are completed on schedule.
  • Support program budgeting, forecasting, resource planning, purchase order tracking, and financial reporting to enable effective execution of CMC development activities.
  • Identify and implement process improvements to strengthen CMC project execution, governance, resource planning, and organizational effectiveness.

Crescent Biopharma develops oncology therapies for solid tumors, focusing on immuno-oncology and targeted approaches. Its lead program, CR-001, is a tetravalent antibody that blocks PD-1 and VEGF to boost anti-tumor immunity while cutting blood vessel growth, and it is in a global Phase 1/2 trial. Additional programs include CR-002, an anti-PD-L1 antibody-drug conjugate, and CR-003, an ITGB6-targeted ADC, creating a multi-modal portfolio. The company differentiates itself by pursuing combination strategies that pair immune checkpoint blockade with VEGF inhibition and other targeted modalities, and its goal is to advance multi-agent regimens for solid tumors toward regulatory approval and commercialization.

Company Size

51-200

Company Stage

IPO

Headquarters

Waltham, Massachusetts

Founded

2003

Get referred to Crescent Biopharma

See people who can refer or advise you

Simplify Jobs

Simplify's Take

What believers are saying

  • July 30, 2026 funding lifted pro forma cash to $305.1 million.
  • ASCEND enrollment progressed in 2026, with first patient dosed February 18, 2026.
  • CR-002 IND submission and first combination trials are scheduled for H2 2026.

What critics are saying

  • CR-001 trails ivonescimab, which beat pembrolizumab in Phase III during 2025-2026.
  • ASCEND's first meaningful readout arrives Q1 2027; failure would crush CBIO's thesis.
  • Three raises since June 2025 signal relentless dilution if trials miss or slow.

What makes Crescent Biopharma unique

  • CR-001 pairs PD-1 and VEGF blockade, targeting a crowded solid-tumor backbone.
  • Kelun-Biotech partnership gives Crescent ex-China rights to SKB105 and China rights to CR-001.
  • June 2025 merger transformed a dead-listing into a cash-rich oncology platform.

Help us improve and share your feedback! Did you find this helpful?

Benefits

Unlimited Paid Time Off

Flexible Work Hours

Remote Work Options

Hybrid Work Options

Parental Leave

401(k) Retirement Plan

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Paid Sick Leave

Paid Holidays

Professional Development Budget

Growth & Insights and Company News

Headcount

6 month growth

-2%

1 year growth

-1%

2 year growth

11%
AllSci
Jul 15th, 2026
Crescent Bio to raise USD 125m to provide oncology pipeline runway into 2028.

Crescent Bio to raise USD 125m to provide oncology pipeline runway into 2028. July 15, 2026 Massachusetts-based Crescent Biopharma, Inc. (Nasdaq: CBIO) announced the pricing of an underwritten public offering of ordinary shares and pre-funded warrants, raising approximately USD 125 million in gross proceeds to fund the clinical advancement of its oncology pipeline, including its lead PD-1 x VEGF bispecific antibody and two ADC programs. The raise extends the company's cash runway, which stood at USD 189 million as of March 31, 2026 and was projected to fund operations into 2028 - a figure that the current offering materially supplements ahead of multiple anticipated data readouts in 2027. The offering comprises 8,094,793 ordinary shares priced at USD 14.50 per share, with pre-funded warrants to purchase up to 525,897 additional shares offered at USD 14.499 per warrant to certain investors in lieu of ordinary shares. Underwriters were granted a 30-day option to purchase up to an additional 1,293,103 ordinary shares at the offering price, which if exercised in full would increase total gross proceeds beyond the USD 125 million base. The offering was expected to close on July 16, 2026. Crescent's pipeline is built around three clinical or near-clinical assets, all developed in partnership with China-based Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. under a bilateral licensing arrangement announced in December 2025 that included an USD 80 million upfront payment by Crescent for ex-China rights to CR-003 and a reciprocal grant to Kelun-Biotech of Greater China rights to CR-001. The lead asset is CR-001, a tetravalent bispecific antibody simultaneously blocking PD-1 and VEGF, currently being evaluated in the global Phase I/II ASCEND trial across multiple solid tumor types including non-small cell lung cancer and gastrointestinal and gynecological cancers. First patient dosing occurred in February 2026. Management has guided for proof-of-concept data - covering initial safety, pharmacokinetics, pharmacodynamics, and preliminary antitumor activity - in Q1 2027, with combination data alongside standard-of-care chemotherapy expected by mid-2027. The first ADC combination trial pairing CR-001 with a Kelun-Biotech ADC is on track to initiate in H2 2026. CR-001 operates in a competitive space alongside ivonescimab, which demonstrated superiority over pembrolizumab in a large Phase III trial, though cross-trial comparisons remain constrained by differences in design and patient populations. CR-002, a PD-L1-targeted ADC with a topoisomerase I inhibitor payload, is on track for IND submission to the US FDA in mid-2026, with Phase I/II trial initiation planned for H2 2026 and proof-of-concept data anticipated in H2 2027. CR-003, an ITGB6-targeted ADC also carrying a topoisomerase I payload, is already in an ongoing Phase I/II trial in China under Kelun-Biotech's sponsorship, with proof-of-concept data expected in Q1 2027. A Phase I/II combination trial of CR-003 and CR-001 is expected to initiate in H1 2027. The current offering is Crescent's third significant capital raise since its June 2025 Nasdaq debut via reverse merger with GlycoMimetics, which was accompanied by a concurrent USD 200 million private placement. A second USD 185 million private placement closed in December 2025 alongside the Kelun-Biotech partnership. The July 2026 public offering represents a shift from institutional private rounds to a broader public equity raise, providing additional capital flexibility as the company approaches its first clinical data milestones. Q1 2026 net loss was USD 23.3 million on R\&D expenses of USD 17.9 million, reflecting accelerating clinical spend as ASCEND enrollment advances and IND preparations for CR-002 proceed. This article was generated with AI assistance and reviewed and edited by the AllSci editorial team Explore more at AllSci News: https://allsci.com/news/

Aktiencheck.de AG
Jul 14th, 2026
Crescent Biopharma launches public offering of ordinary shares and pre-funded warrants

Crescent Biopharma, a clinical-stage biotechnology company focused on cancer therapies, announced it has launched an underwritten public offering of ordinary shares and pre-funded warrants. The Waltham, Massachusetts-based company plans to grant underwriters a 30-day option to purchase up to an additional 15% of ordinary shares at the public offering price, less underwriting discounts and commissions. All securities in the proposed offering will be sold by Crescent. The offering is subject to market and other conditions, with no assurance regarding completion timing or final size and terms.

GlobeNewswire
Jul 14th, 2026
Crescent Biopharma Announces Proposed Public Offering of Ordinary Shares and Pre-Funded Warrants

WALTHAM, Mass., July 14, 2026 (GLOBE NEWSWIRE) -- Crescent Biopharma, Inc. (“Crescent” or the “Company”) (Nasdaq: CBIO), a clinical-stage biotechnology...

Business Wire
Jun 27th, 2026
GlycoMimetics Enters Into Acquisition Agreement With Crescent Biopharma

GlycoMimetics, Inc. (NASDAQ: GLYC) announced today it has entered into an acquisition agreement with Crescent Biopharma, Inc. (“Crescent”), a privately held ...

AD HOC NEWS
Feb 7th, 2026
Fidelity takes 15% stake in Crescent Biopharma ahead of key industry summit

Fidelity has taken a 15% stake in Crescent Biopharma, accumulating approximately 4.13 million shares as of year-end, according to regulatory filings. The investment from one of the world's largest asset managers signals institutional confidence in the biotech company's strategic direction. The stake disclosure comes ahead of Crescent's appearance at the Guggenheim Emerging Outlook: Biotech Summit 2026 in New York on 12 February. The company's executive team will participate in a fireside chat at 11:30 EDT, with a live webcast available for remote viewers. Crescent shares closed at $9.51 on Thursday, down 3.09%, but trading volume of 510,788 shares significantly exceeded the 20-day average of 198,000, suggesting investors are positioning ahead of the conference presentation.