Apogee Therapeutics

Senior Director, Statistical Programming

Lead statistical programming with 12-15 years of clinical trial programming; SAS/CDISC expertise; regulatory submissions; remote work experience; strong leadership and collaboration.

Senior Manager, Clinical Biomarker Operations

Lead biomarker operations, manage sample logistics, CRO oversight, and collaborate across functions.

Director, GMP Quality Assurance

10+ years GMP QA in biotech/pharma; audits; CDMO oversight; FDA/EMA/ICH; QMS; travel up to 20%.

Senior Manager, Regulatory Affairs

BS/MS/PhD in regulatory affairs or related scientific field; RAC preferred; 5+ years regulatory drug development experience; FDA/EMA experience; strong PM and communication; Veeva RIM, eCTD, and Office tools experience; aligns with Apogee’s CORE values; travel up to 10%.

MS or BS with biomarker operations experience; CRO oversight; clinical trials; travel; collaboration.

Senior Manager, Clinical Systems

10+ years leading clinical systems programs in biotech/pharma; experience with IRT, CTMS, eCOA, LMS; strong PM skills and SDLC knowledge.

Executive Director, GMP Quality Assurance

Executive Director

15+ years GMP QA experience; leadership of QA organizations; manage external partners; develop and scale QA systems and risk management; strong communication.

Associate Director, Analytical Development

PhD in Analytical Chemistry, Biochemistry, or related field; 7+ years in analytical development for monoclonal antibodies/biologics; strong MS, HPLC/UPLC, and biophysical method expertise; experience with external CRO/CDMO partners; travel up to 35%; hybrid work model.

Associate Director, Clinical Operations Standards and Planning

12+ years in clinical operations in pharma/biotech; BS degree; experience overseeing CROs/vendors; global trials; process optimization and standardization.

Clinical Trial Manager

Bachelor’s degree in life sciences; 5+ years clinical trial management experience in international Phase II/III trials; strong ICH/GCP knowledge; vendor management; travel up to 35%.

Associate Director, Clinical Supply Chain Management

12+ years in supply chain; 5+ years leadership; biotech/pharma exp; global clinical trials; import/export; GMP/ICH/CFR knowledge; Excel/forecasting tools; leadership.

Associate Director, Statistical Programming

10+ years in clinical trial programming; advanced SAS; R; CDISC SDTM/ADaM; experience managing CROs and remote teams.

Regional Director, Field Medical Affairs - East

Regional Director, Field Medical Affairs

Advanced scientific degree with 7+ years Medical Affairs and 5+ years field medical; MSL leadership; dermatology experience; strong communication; up to 75% travel.

Senior Manager, Regulatory Affairs Project Management

Regulatory Affairs Project Management

5+ years in pharmaceutical/biotech project management with regulatory submissions (IND/CTA, BLA/NDA/MAA); strong Smartsheet proficiency; global regulatory experience; willing to travel up to 20%

Manager, Clinical Business Operations

Bachelor's in science; 10+ years in biotech/pharma; 3+ years in Clinical Operations; experience across PhI-PhIII; proficient with Smartsheet/Microsoft Project; willing to travel up to 15%.

Senior Manager, Scientific Communications, Planning & Operations

Bachelor's in life sciences; 5+ years in medical/scientific communications, operations, or congress planning; strong PM skills; ML/R review knowledge; experience with publication/review systems; ISMPP familiarity; travel up to 10%.

Senior Director, Commercial Strategy

Director, Commercial Strategy

Approximately 10+ years in industry, including 5+ years in strategic consulting or biotech/pharma strategy; strong commercial strategy experience; remote-capable with up to 20% travel.

Clinical Monitoring Manager

Bachelor's degree in a scientific field; 8+ years as a CRA; 2+ years leading a team; travel up to 35%; CCRA preferred; strong knowledge of ICH/GCP/FDA; proficient with EDC/eTMF and MS Office/Smartsheet.

Associate Director, Data Management

Data Management

Bachelor’s degree; 8+ years clinical data management; experience with data management systems and regulatory requirements; strong CRO/vendor management; NDA/sNDA/BLA submissions; GCP knowledge; EDC/eCOA experience; excellent communication; remote work readiness.

Associate Director, Quality Control – Analytical Sciences 

Associate Director, Quality Control

Lead QC Analytical Sciences with 7+ years of analytical development and QC experience; strong regulatory knowledge; cross-functional collaboration; travel up to 30%.

Director, Drug Product Development

10+ years in drug product development/manufacturing; 5+ years in GMP ops for PFS; leadership in GMP manufacturing of combination products; PhD or equivalent experience; strong cross-functional collaboration and regulatory involvement.

Associate Director, Manufacturing Science and Technology 

PhD or equivalent experience; 7+ years biologics development/manufacturing; experience with late-phase monoclonal antibodies; tech transfer to CDMOs; DS campaigns through scale-up and PPQ; strong cross-functional collaboration.

Associate Director, Biostatistics

Biostatistician

Lead statistical design and analysis for clinical studies; manage CROs; 8+ years in drug development statistics; PhD preferred or MS with relevant experience.

Title	Location	Date
Senior Director, Statistical Programming Full Time · $270K-$295K · 12+ YOE United States · Remote	United States Remote	Apr 30, 2026
Senior Manager, Clinical Biomarker Operations Full Time · $150K-$170K · 3+ YOE United States · Remote	United States Remote	Apr 29, 2026
Director, GMP Quality Assurance Full Time · $210K-$235K · 10+ YOE United States · Remote	United States Remote	Apr 27, 2026
Senior Manager, Regulatory Affairs Full Time · $155K-$175K · 5+ YOE United States · Remote	United States Remote	Apr 24, 2026
Senior Manager, Clinical Biomarker Operations Full Time · $150K-$170K · 3+ YOE United States · Remote	United States Remote	Apr 22, 2026
Senior Manager, Clinical Systems Full Time · $150K-$165K · 10+ YOE United States · Remote	United States Remote	Apr 22, 2026
Executive Director, GMP Quality Assurance Full Time · $275K-$305K · 15+ YOE United States · Remote	United States Remote	Apr 17, 2026
Associate Director, Analytical Development Full Time · $175K-$195K · 7+ YOE Boston or Remote · Hybrid	Boston or Remote Hybrid	Apr 13, 2026
Associate Director, Clinical Operations Standards and Planning Full Time · $175K-$195K · 12+ YOE United States · Remote	United States Remote	Apr 6, 2026
Clinical Trial Manager Full Time · 5+ YOE United States · Remote	United States Remote	Apr 2, 2026
Associate Director, Clinical Supply Chain Management Full Time · $170K-$190K · 12+ YOE United States · Remote	United States Remote	Apr 2, 2026
Associate Director, Statistical Programming Full Time · $190K-$210K · 10+ YOE United States · Remote	United States Remote	Apr 2, 2026
Regional Director, Field Medical Affairs - East Full Time · $250K-$280K · 7+ YOE United States · Remote	United States Remote	Apr 1, 2026
Senior Manager, Regulatory Affairs Project Management Full Time · $150K-$170K · 5+ YOE United States · Remote	United States Remote	Mar 19, 2026
Manager, Clinical Business Operations Full Time · $145K-$160K · 10+ YOE United States · Remote	United States Remote	Mar 13, 2026
Senior Manager, Scientific Communications, Planning & Operations Full Time · $155K-$175K · 5+ YOE United States · Remote	United States Remote	Mar 13, 2026
Senior Director, Commercial Strategy Full Time · $255K-$285K · 10+ YOE United States · Remote	United States Remote	Mar 12, 2026
Clinical Monitoring Manager Full Time · $150K-$170K · 8+ YOE United States · Remote	United States Remote	Mar 2, 2026
Associate Director, Data Management Full Time · $180K-$195K · 8+ YOE United States · Remote	United States Remote	Feb 23, 2026
Associate Director, Quality Control – Analytical Sciences Full Time · $165K-$185K · 7+ YOE United States · Remote	United States Remote	Jan 12, 2026
Director, Drug Product Development Full Time · $210K-$235K · 10+ YOE United States · Remote	United States Remote	Jan 12, 2026
Associate Director, Manufacturing Science and Technology Full Time · $175K-$195K · 7+ YOE United States · Remote	United States Remote	Jan 9, 2026
Associate Director, Biostatistics Full Time · $195K-$215K · 8+ YOE United States · Remote	United States Remote	Jan 5, 2026

Activities	Biopharmaceutical research and developmentClinical-stage drug developmentAntibody engineeringBiologics manufacturingTherapeutic clinical trials
Headquarters	US
Industries	BiotechnologyPharmaceuticals
Name	Apogee Therapeutics
Employees	196
Type	Public
Tagline	Develops engineered biologics for inflammatory and immunological diseases.
Founded	2,022
Website	apogeetherapeutics.com
Stock Exchange	NASDAQ
Stock Symbol	APGE

Apogee Therapeutics

About Apogee Therapeutics