The successful candidate will maintain the Interactive Technologies Systems and all associated elements. Role & Responsibility Perform changes/updates to ICOPho...
COMPANY INFO: NOW HIRING!! Are you looking to expand your career and enhance your professional skills? MedFocus is now seeking a Regulatory Affairs Associate Ou...
COMPANY INFO: NOW HIRING!! Are you looking to expand your career and enhance your professional skills? MedFocus is now seeking an EHS Manager Our client is deve...
COMPANY INFO: NOW HIRING!! Are you looking to expand your career and enhance your professional skills? MedFocus is now seeking a Clinical Marketing Manager Our ...
The successful candidate will maintain the Interactive Technologies Systems and all associated elements. Role & Responsibility Perform changes/updates to ICOPho...
Our Company We are a rapidly growing pharmaceutical manufacturer with strong lines in hospital and ophthalmic markets, and many new products in development and ...
Summary: The CMC Global Lead will manage projects within the Global Biologics R&D organization with overall responsibility of coordinating CMC activities betwee...
Summary: With supervision as required, proficiently performs all assigned chemistry techniques. Demonstrates a good understanding of scientific principals and t...
Summary: Develop global registration strategy for new products and manage the submission process to secure expeditiously registration in a cost effective manner...
Our Company We are a rapidly growing pharmaceutical manufacturer with strong lines in hospital and ophthalmic markets, and many new products in development and ...
Summary: The Medical Communications Department's objective is the dissemination of all or any medical/technical information regarding all Hospira products upon ...
Summary: Oversees the registrations of products in countries outside the US that they are in compliance with applicable regulations, are appropriately documente...
Summary: Assures that new products are developed in line with the global registration requirements of targeted countries and obtains expedient registration of t...
Summary: The Operations Sr. Regulatory Associate is responsible for the assembly, quality control and dissemination of data and documentation to regulatory agen...
Summary: In collaboration with the customer, develops product strategies to bring product to market and maintain them over their product lifecycle. Will provide...
COMPANY INFO: NOW HIRING!! Are you looking to expand your career and enhance your professional skills? MedFocus is now seeking a Clinical Project Manager Our cl...
Job Description: Experienced data management professional who is responsible for all activities relating to over 20 studies over the course of 1 year. The prima...
Our Client has an opening for a Clinical Study Manager in Abbott Park, IL. It is for 3 months Contract- Right to hire. ( Sponsorship is not available) Client wi...
PRIMARY JOB FUNCTION: The Lead Management, Licensing Opportunity Licensing Opportunity and Contract Database coordination, including data entry/updates, triage/...
Primarily provides search and analysis as needed of patents and published literature related to biology/biotechnology subject matter including diagnostic and mo...