Jobs at Rhythm Pharmaceuticals

Supports pharmaceutical QA and regulatory compliance for clinical and commercial products. Responsibilities include batch release documentation, GMP/GDP record review, quality event tracking, document workflows, supplier qualification records, quality metrics, audit readiness, and inspection preparation. The role collaborates with Qualified Persons, Technical Operations, Supply Chain, Regulatory Affairs, and external partners while identifying documentation gaps and maintaining compliant quality systems.

Serve as Switzerland’s Responsible Person under the Swissmedic Wholesale Distribution License, ensuring GDP compliance, product quality, inspections, recalls, CAPAs, audits, training, and regulatory communications. Support global GDP operations through Veeva documentation, batch disposition, quality events, temperature excursions, audits, procedures, change controls, and cross-functional launch readiness. Manage outsourced GDP activities, suppliers, 3PLs, and Swiss-specific quality systems within a global biotech organization.

Supports safety science across clinical development and post-approval products, leading aggregate safety surveillance, signal detection and management, risk-benefit assessments, and safety data interpretation. Prepares global pharmacovigilance documents including PBRERs, PSURs, DSURs, and RMPs; contributes to clinical and regulatory documents; improves PV processes, compliance, and data quality; and mentors staff and vendors.

Lead Qualified Person activities and GMP/GDP quality assurance for investigational and commercial medicinal products. Responsibilities include batch certification and release, supply-chain oversight, deviation and CAPA management, audits, quality agreements, inspection readiness, regulatory compliance, and cross-functional support across manufacturing, clinical, commercial, and distribution operations.

Supports international employees and leaders across Italy, Spain, marketing, market access, and medical teams. Advises on organizational effectiveness, workforce planning, talent management, employee relations, performance, recruitment, development, compliance, benefits, and change management. Partners with leadership, payroll, legal counsel, vendors, and HR teams to implement regional people strategies, policies, and programs while ensuring legal and ethical compliance across multiple countries.

Leads pharmaceutical brand strategy, localization, and marketing execution across Spain and Portugal. Develops omnichannel campaigns, promotional programs, patient and HCP initiatives, events, and congresses. Coordinates with medical, sales, legal, regulatory, agencies, and international marketing teams to ensure compliant execution. Manages budgets, KPIs, performance analytics, stakeholder relationships, and the marketing-to-sales handoff while optimizing regional tactics and customer experience.

Leads global compensation strategy, benchmarking, salary structures, pay transparency, annual compensation cycles, incentive and equity programs, NQDC administration, regulatory compliance, and process improvements. Partners with HR, Talent Acquisition, Finance, and business leaders to support job evaluations, offers, promotions, pay equity, data integrity, and employee communications across a global organization.

Manage specialty pharmaceutical sales for IMCIVREE, focused on acquired hypothalamic obesity across Minnesota, North Dakota, South Dakota, and parts of Wisconsin. Educate healthcare professionals, build specialist relationships, support patient enrollment and adherence, collaborate with medical and marketing teams, present at industry congresses, maintain CRM data, manage territory budgets, and meet compliance and administrative requirements. The role requires frequent travel and residence in Minneapolis.

Manages scientific publication activities across integrated publication plans, coordinating authors, vendors, internal stakeholders, submissions, documentation, timelines, budgets, and congress materials. Ensures compliance with publication standards, maintains accurate records, tracks milestones, resolves operational issues, and improves processes. The role supports medical affairs and publication teams in a pharmaceutical environment.

Oversee accurate, compliant monthly payroll across international markets, especially Europe. Responsibilities include payroll processing, input validation, reconciliation, vendor coordination, statutory compliance, employee inquiries, audits, reporting, system enhancements, process improvement, and support for new market entities. The role partners closely with HR, Finance, payroll providers, and local authorities while managing sensitive payroll and compliance matters.

Provides statistical programming support for clinical studies, regulatory submissions, and integrated analyses. Develops, validates, and maintains ADaM datasets, tables, listings, figures, specifications, macros, and submission documentation using SAS and CDISC standards. Partners with cross-functional teams and vendors, supports submission readiness, resolves programming risks, improves processes, and may mentor programmers, oversee vendors, and contribute to departmental standards.

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

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.

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.

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 (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 the Eastern Canada territory across Quebec and Atlantic provinces for a specialty biopharmaceutical company. Develop territory business plans, achieve sales targets, build relationships with healthcare professionals, communicate clinical information, execute educational and conference activities, report CRM data, manage budgets, and maintain compliance. The role requires frequent field travel, French and English fluency, and at least six years of specialty pharmaceutical or biotech sales experience.

Serves as statistical lead for clinical studies and program activities, supporting study design, sample size calculations, SAPs, analyses, TLFs, interim analyses, regulatory submissions, and interpretation of results. Collaborates with clinical, regulatory, safety, data management, programming, and external vendor teams. Reviews statistical outputs, ensures quality and compliance, contributes to inspection readiness, and supports process improvements in a fast-paced biotech environment.

Leads biostatistical strategy for clinical development programs, including study design, sample size calculations, protocols, SAPs, analyses, TLFs, regulatory submissions, interim analyses, and interpretation of results. Collaborates with clinical, regulatory, safety, data management, programming, and medical writing teams; oversees statistical vendors; supports publications and process improvements; and provides strategic leadership in a dynamic biotech environment.