Top Pharmaceutical Jobs in Boston, MA

The Sales Representative promotes and sells Ferring products, manages customer relationships, achieves sales quotas, and represents the company at industry meetings.

The Regional Sales Specialist in Uro-Oncology will promote Ferring's intravesical gene therapy to healthcare professionals, aiming to achieve sales quotas through effective customer engagement and collaboration with cross-functional teams.

The Associate Director will lead the Transparency Reporting program, ensuring compliance and governance while managing global reporting initiatives and collaborating with various business units.

Lead the delivery of accurate and compliant payroll for U.S. employees, manage day-to-day payroll vendor relationships, and ensure payroll processes support compliance and employee trust.

The Director will lead media and digital initiatives in Therapeutic Dermatology, focusing on strategy development, performance optimization, and cross-functional collaboration while promoting innovation in engagement.

Responsible for managing regional sales activities, leading sales professionals to exceed objectives, analyzing sales data, and mentoring team members.

The Executive Director oversees chapter operations, manages staff, ensures alignment with CF Foundation's mission, and develops fundraising strategies.

The Vice President, Program Management oversees Kymera's Program Management Office, ensuring program strategies are optimized and effectively organized for decision-making. Responsibilities include leading program management support, resource allocation, fostering high-performance teams, and driving major scaling initiatives in drug development and commercialization.

The Associate Director, GCP Quality ensures compliance with GCP across clinical trials, providing quality oversight, risk management, and training.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

As a Clinical Research Associate, you will conduct clinical trial monitoring, ensure protocol compliance, analyze data, and collaborate with site staff.

As a Senior Clinical Research Associate, you will oversee clinical trials, ensuring adherence to protocols and regulatory standards, managing multiple sites, and collaborating with teams for data integrity and compliance.

The Product Manager II will lead the product roadmap and development for molecule design products, focusing on GenAI capabilities and collaboration with R&D stakeholders for innovative solutions.

The Senior Governance Engineer will design and deploy governance solutions, ensure compliance, collaborate with teams, and mentor junior members in GSK's data governance initiatives.

Responsible for leading statistical programming activities, managing programmers, ensuring quality and timeliness of deliverables, and collaborating across functions for drug development.

The Director, Global Labeling leads the Labeling function within Global Regulatory Services, managing operations, developing labeling strategies, and mentoring a team across the US and UK.

The Director of Program Management will lead and support the development and manufacturing of small molecule programs, coordinating with internal teams and external contractors to ensure project deliverables are met on time and within scope.