Jobs at Rhythm Pharmaceuticals

The Territory Manager will oversee sales of IMCIVREE® for Acquired Hypothalamic Obesity, ensuring compliance with education provided to healthcare professionals and fostering strong relationships with specialists.

Lead end-to-end development and lifecycle management of drug-device combination products (prefilled syringes, auto-injectors). Own DHF and design controls, drive verification/validation, human factors, risk management, regulatory support, and manufacturing tech transfer. Manage cross-functional teams and external vendors/CDMOs to deliver patient-centric, compliant devices from late-stage development through commercialization.

The Territory Manager will develop business plans, achieve sales targets, foster relationships with healthcare professionals, manage budget allocations, and ensure compliance, while traveling extensively in the Canada West Region.

Field-based territory manager responsible for promoting IMCIVREE for Bardet-Biedl syndrome across a Northwest territory. Build relationships with specialists, deliver disease and branded education, support prescriber enrollment and patient services, collaborate with MSL and marketing, maintain CRM records, and meet sales objectives while complying with regulatory and company standards. Heavy travel and budget management required.

The Director of Nonclinical Development leads and executes nonclinical strategies, manages CRO relationships, and contributes to regulatory submissions for clinical programs.

The Territory Manager will lead sales efforts for IMCIVREE®, provide education to healthcare providers, develop relationships, and ensure compliance in the Florida area.

The Territory Manager will handle sales for IMCIVREE® focused on Bardet-Biedl syndrome, educate HCPs, and develop physician relationships while ensuring compliance and operational responsibilities.

The Territory Manager is responsible for sales of IMCIVREE®, focusing on disease education, building relationships with healthcare professionals, and supporting marketing initiatives while ensuring compliance with company standards.

Develop, validate, and QC analysis datasets, tables, listings, and figures for clinical studies and regulatory submissions. Create ADaM specs, TLF shells, reusable macros, and submission-ready documentation (define.xml, reviewer guides). Partner with Biostatistics, Data Management, Clinical Development, and vendors; identify risks, drive process improvements, and mentor junior programmers as needed.

Provide strategic and technical leadership for analytical development and QC across the product lifecycle. Define control strategies, lead method development/validation/transfer, oversee stability and impurity programs, ensure cGMP/data integrity compliance, manage CDMO/CRO partnerships, support regulatory CMC submissions and inspections, and build a high-performing analytical organization.

The Treasury Manager oversees cash operations, banking administration, compliance, financial analysis, and partnerships to optimize liquidity and streamline treasury functions.

The Head of Global Strategic Sourcing leads the strategic sourcing function, manages supplier relationships, and ensures alignment with business objectives. Responsibilities include executing sourcing vision, optimizing costs, building supplier partnerships, and establishing governance frameworks.

The (Senior) Brand Manager for GSA will lead and execute localized marketing strategies, oversee integrated initiatives, manage compliance, build stakeholder relationships, and analyze performance metrics.

Manage U.S. multi-state payrolls for 270+ employees and Canadian payroll. Ensure compliance with tax laws and improve payroll processes.

Provide legal support for global clinical operations including drafting, reviewing, and negotiating clinical trial contracts (CROs, sites, vendors), lead CLM processes and playbooks, advise business leaders on risk-based strategies, manage outside counsel, and contribute to cross-functional life sciences legal matters.

Lead design, execution, and interpretation of mechanistic and translational in vitro and in vivo studies via CROs and collaborators to inform discovery and early-stage development. Identify and prioritize exploratory biology initiatives, develop hypotheses and assays, integrate multidisciplinary data, guide program strategy, and communicate findings to senior leadership while managing external partners and cross-functional teams.

Lead GCP/GLP/GVP quality oversight for clinical studies, manage QMS and vendor audit programs, develop SOPs and training, support regulatory inspections, review clinical and safety documents, identify and mitigate compliance risks, and partner cross-functionally to ensure GCP compliance and quality across programs.

Lead data management for multiple clinical studies and/or a development program. Oversee CRO-managed data activities, ensure timelines and data quality, develop DM metrics and SOPs, support vendor qualification and audits, drive inspection readiness and submissions, mentor staff, and contribute to operational improvements and hands-on data management as needed.

The Territory Manager will be responsible for sales of IMCIVREE® in Acquired Hypothalamic Obesity, educating healthcare providers, and ensuring compliance with company standards while developing strong relationships in the assigned territory.

Manage day-to-day administration of Veeva QDocs/eQMS, support GxP document lifecycle and end-user troubleshooting, implement QMS improvements, assist complaint intake, coordinate training, participate in GxP IT system validation, perform supplier audits, and support inspection readiness to ensure GMP/GDP compliance for clinical and commercial products.