Jobs at Summit Therapeutics | HiringCafe

Summit Therapeutics

Lead, Regional Medical Science Director

Medical Science Director

Doctoral degree in health sciences; 5+ years solid tumor experience; 2+ years Medical Science Liaison; HCIR credentialing; willing to travel up to 75%.

Senior Medical Science Liaison

Doctoral degree; 5+ years solid tumor oncology; 2+ years MSL; travel up to 75%; strong communication and collaboration.

Doctoral degree in health sciences; 5+ years solid tumor oncology; 2+ years as an MSL; willing to travel up to 75%; pharma experience preferred.

Senior Medical Science Liaison 

Doctoral degree in health sciences; 5+ years solid tumor oncology; 2+ years MSL; willing to travel 75%; strong communication and relationship-building; HCIR credentialing.

Senior Director of Technical QA (GMP)

Director of Technical QA

15+ years in pharma with 8+ in commercial manufacturing; biologics GMP experience; strong QMS and regulatory submission expertise; CMOs management; strong communication.

Vice President, US Marketing

Marketing

15+ years pharma marketing; US launch leadership; MBA/PhD preferred; oncology experience; strong leadership and digital marketing.

Associate Director, Regulatory CMC

Bachelor’s degree in chemistry, pharmacy, engineering, or biochemistry; 6+ years Regulatory CMC experience; experience with biologics; strong FDA/EU regulatory knowledge; experience preparing CMC submissions (IND/IMPD/BLA/MAA). Mandarin desirable.

Senior Principal Engineer/Associate Director, Drug Product MSAT

Drug Product MSAT

10+ years life sciences MSAT/sterile DP experience; tech transfer, regulatory writing, cross-functional collaboration.

Senior Manager, Clinical Site Partner (CSP)

Senior Manager, Clinical Site Partner

Bachelor’s degree in a scientific or medical discipline; 8+ years of clinical research experience; extensive oncology late-stage trial experience; US site management and travel up to 75%.

Executive Director, US Market Access Strategy

12+ years market access in oncology; NSCLC experience; BS/BA; US payer relationships; pricing/HEOR experience; willing to travel.

Clinical Trial Manager

Bachelor’s degree preferred; 5+ years clinical project management in international trials; oncology experience; budget and vendor management; travel required.

Clinical Supplies Manager

Experience in clinical supply planning, forecasting, vendor and inventory management in pharma; GMP/regulatory compliance; cross-functional collaboration.

Principal Statistical Analyst

Bachelor’s or Master’s in Biostatistics, Statistics, or Computer Science; 7+ years pharma programming; SAS, CDISC (SDTM/ADaM); regulatory knowledge; Docker; R/Python; SQL; leadership experience.

Sr. Commercial Attorney, Transactions

Commercial Attorney

JD; 8+ years pharma industry in-house or big law; extensive contract negotiation/drafting; regulatory/compliance knowledge; product launches experience; strong communication.

Senior Manager, Data Scientist

Data Scientist

5+ years in data science; biotech/pharma experience; Python/R; SQL; ML; strong communication.

Senior Manager, Clinical Data Management 

8+ yrs in clinical data management, 3+ yrs in leadership; Medidata Rave EDC expert; CRO/vendor oversight; oncology Phase III exp; FDA/ICH/GCP/CDISC knowledge.

Senior Director, Sales Operations (Oncology)

Sales Operations

12+ years Commercial/Sales Operations in Pharma/Biotech; oncology experience preferred; strong CRM/analytics; leadership and cross-functional collaboration.

Senior Medical Liaison (PA, NJ)

Senior Medical Liaison

Doctoral degree in health sciences; 5+ years solid tumor oncology experience; 2+ years in Medical Science Liaison; travel up to 75%; HCIR credentialing.

7+ years pharmaceutical/biotech programming; SAS, CDISC SDTM/ADaM; oncology trials preferred; data manipulation, dashboards, regulatory documentation.

Manager, Quality Assurance (GMP)

Quality Assurance Manager

Lead GMP QA activities, ensure compliance with FDA/EMA/ICH, manage audits, CAPAs, batch review, cross-functional collaboration.

Director, Medical Affairs, Lung

Director, Medical Affairs

MD/PhD/PharmD required; 6+ years medical affairs; oncology launch experience preferred; strong analytics and communication; travel 20-30%.

Director, Statistical Programming

Director of Statistical Programming

PhD with 8+ years or MS with 11+ years in statistics/biostatistics with clinical trials; oncology experience; CDISC; SAS/R; ICH/FDA/GCP knowledge; strong communication and leadership.

Director, Marketing Operations

Bachelor’s degree; 10+ years in marketing operations within biotech/pharma; strong MLR/compliance; digital marketing ops and tech ecosystem leadership.

Director, Market Access Payer Accounts

Director

10+ years biotech/pharma experience; 5+ years oncology payer account management; bachelor's in business/healthcare; advanced degree preferred; strong leadership and negotiation; US payer exposure.

Director, Clinical Scientist

Lead/contribute to study design and execution of clinical oncology/hematology studies; collaborate with regulatory, operations, and CROs; strong data interpretation and communication.

Associate Director, Clinical Data Management

10+ years in Clinical Data Management, oncology focus, leadership of CDM staff/CROs, experience with EDC, data standards, regulatory compliance.

Accounting Manager, R&D (Non-Clinical)

Accounting Manager

Bachelor’s in Accounting/Finance; 5+ years in accounting; R&D accrual experience in biotech/pharma; cross-functional collaboration; global accounting experience; NetSuite; FloQast; Agiloft; MS Office.