This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Lead regulatory labelling strategy for medicinal products in Hertfordshire. Develop and maintain Core Data Sheets and EU/US product information, ensuring global compliance. Collaborate cross-functionally, providing strategic guidance throughout the product lifecycle. Requires strong regulatory af...
Location
United Kingdom , Hertfordshire
Salary
Not provided
Proclinical
Expiration Date
Until further notice
Regulatory Program Manager
Lead regulatory lifecycle management projects in Paris, driving pharmaceutical innovation. Coordinate cross-functional CMC, regulatory, and supply teams to advance a portfolio of products. Ideal candidates have strong project management and CMC expertise within the pharma industry.
Location
France , Paris
Salary
Not provided
Proclinical
Expiration Date
Until further notice
EHS Project Manager
Join our team as an EHS Project Manager in Lexington, MA. You will develop and implement critical safety programs for facilities and construction projects within biotech/pharma. This role requires strong EHS regulatory knowledge and experience with risk assessment and management systems. We seek ...
Location
United States , Lexington
Salary
90.00 - 95.00 USD / Hour
Proclinical
Expiration Date
Until further notice
Automation Technician
Join a global CMO as an Automation Technician in Neuchâtel. Provide vital technical support for OT infrastructure, cybersecurity, and process control systems (PCS). Utilize your expertise in GMP, SCADA, and industrial networks to ensure compliance and seamless operations. This role offers a colla...
Location
Switzerland , Neuchâtel
Salary
Not provided
Proclinical
Expiration Date
Until further notice
Project Manager
Lead the development of Companion Diagnostics (CDx) from concept to care as a Project Manager in Tucson. You will create integrated plans, manage budgets, and mitigate risks to drive project execution. This role requires strong PM expertise to guide cross-functional teams and ensure quality throu...
Location
United States , Tucson
Salary
Not provided
Proclinical
Expiration Date
Until further notice
Assistant Scientist - QC Micro
Location
United States , Zebulon
Salary
Not provided
Proclinical
Expiration Date
Until further notice
QA Validation, Senior Associate
Location
United States , Boston
Salary
90.00 - 97.00 USD / Hour
Proclinical
Expiration Date
Until further notice
Senior Project Manager
Location
United States , San Diego
Salary
75.00 - 90.00 USD / Hour
Proclinical
Expiration Date
Until further notice
QA Consultant
Location
United States , Durham
Salary
Not provided
Proclinical
Expiration Date
Until further notice
Medical Director, Hematology
Location
United States , Boston
Salary
Not provided
Proclinical
Expiration Date
Until further notice
Veeva Clinical Business Administration Specialist
Join our Boston team as a Veeva Clinical Business Administration Specialist. You will optimize Veeva Vault Clinical systems, providing crucial user support and driving process improvements. The role requires expertise in eTMF/CTMS, system validation, and clinical trial processes. This is a key op...
Location
United States , Boston
Salary
Not provided
Proclinical
Expiration Date
Until further notice
Medical Writing Operations Manager
Lead document quality and submission readiness for a top pharmaceutical firm in Cambridge, US. Utilize your regulatory publishing expertise to manage and QC clinical documents like CSRs and IBs, ensuring eCTD compliance. This role demands sharp detail-orientation and proficiency in MS Office/Adob...
Location
United States , Cambridge
Salary
70.00 - 77.00 USD / Hour
Proclinical
Expiration Date
Until further notice
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