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Manager, Inpatient Pharmacy Services
CAMBRIDGE, MASSACHUSETTS, UNITED STATES
...physicians. The Manager of Inpatient Pharmacy Services for Cambridge/Somerville Hospitals is responsible for managing the day-to-day activities of two of our three inpatient pharmacies, which includes a staff of 14 pharmacists, 4 PGY1 pharmacy residents, 13 pharmacy technicians and...
Senior GxP Project Manager
CAMBRIDGE, MA, UNITED STATES
Location: Cambridge, MA (Hybrid)Zifo is looking for a Project Manager with understanding of and experience in GxP processes for a client in Cambridge, MA. The Project Manager will be responsible for the delivery of various technical solutions.RequirementsHigh level PM Job Description...
Senior Manager, Regulatory CMC Lead
CAMBRIDGE, MA, UNITED STATES
Job DescriptionAbout This Role This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsibilities include preparation and compilation of...
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M&A Project Manager
CAMBRIDGE, MA, UNITED STATES
Client is seeking a full-time contract Project Manager based in the U.S. to manage upcoming M & A integration projects. These projects may be a full company integration or an asset integration. Remote (Local to Cambridge, MA for occasional visit), 37.5 Hours per weekBioMedical...
Regulatory Affairs Manager III
CAMBRIDGE, MA, UNITED STATES
The Fountain Group are a national staffing firm and are currently seeking a Regulatory Affairs Manager III for a prominent Pharmaceutical client of ours. This position is Remote. Details for the position are as follows: Job Description:Pay: 75.00-86.54/hr on W2.6-month assignment to start...
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Regulatory Affairs Manager
CAMBRIDGE, MA, UNITED STATES
Responsibilities: However, they will mainly fall within the areas of Pharmaceutical, Biotechnology or Biologics Regulatory Affairs This individual will prepare, compile, and submit CT/IND/MAA I NOA, manage and implement label review, translation requirements, fee requirements, and may...
CMC Regulatory Affairs Program Manager
CAMBRIDGE, MA, UNITED STATES
Responsibilities: Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality guidelines to ensure that the current and phase appropriate requirements and standards are properly and timely implemented. Provide...
Senior Clinical Data Manager
CAMBRIDGE, MA, UNITED STATES
...Senior Clinical Data Manager to join their growing team. In this role, you will play a crucial part in overseeing the clinical data management process, ensuring the integrity and quality of clinical trial data. If you are a dedicated professional with a strong background in clinical data...
Senior Product Manager, HCP Marketing (MS Franchise)
CAMBRIDGE, MA, UNITED STATES
Job DescriptionAbout This RoleReporting to the Sr. Director of HCP Marketing, the Senior Product Manager, HCP Marketing will drive key HCP marketing initiatives to drive growth for Biogen s MS brands. What You ll Do Ensure specific HCP initiatives including marketing programs and...
Associate Director, Enterprise Risk Management
CAMBRIDGE, MA, UNITED STATES
...assets, and maintain regulatory compliance in a dynamic industry.What You ll DoRisk Assessment and Analysis:Mature processes to identify and assess potential risks across all areas of Biogen, including financial, operational, strategic, compliance and reputational risks. Collaborate...
Engineer
CAMBRIDGE, MA, UNITED STATES
...Combination ProductsRegulatory StandardsProblem Solving / Root Cause AnalysisStrong individual contributorCollaborative team playerFast and continuous learnerFlexible/highly adaptive to continuous changing priorities/environment Top 3 Must Have Skill Sets:Effective Communicator...
Director of Information Security
CAMBRIDGE, MASSACHUSETTS, US
...oversight of technical regulatory and compliance requirements. Ensure security is embedded in the minds and culture of all employees. This includes being involved with our community and continuously driving awareness through training, conversations, presentations, etc. Help manage vendor...
Senior Director, Total Rewards
CAMBRIDGE, MASSACHUSETTS, US
...plan compliance with regulatory filings and updates, notices, ACA mandates & reporting, plan audits, and non-discrimination testing. Prepare audit documentation to ensure SOX compliance. With an eye for important regulations, ensure all CarGurus-related administrative forms, reports, processes...
Clinical Research Associate
CAMBRIDGE, MA, UNITED STATES
...with the Clinical Trial Manager has responsibility to assist and support for all study management aspects of assigned Client Lab studies or may manage a unique part of studies (e.g. recruitment, scheduling, and ISF filing).This individual provides operational support to teams from study startup...
Clinical Research Associate
CAMBRIDGE, MA, UNITED STATES
...with the Clinical Trial Manager has responsibility to assist and support for all study management aspects of assigned Client Lab studies or may manage a unique part of studies (e.g. recruitment, scheduling, and ISF filing).This individual provides operational support to teams from study startup...
Engineer
CAMBRIDGE, MA, UNITED STATES
...priorities \" Design Controls / Combination Products \" Regulatory Standards \" Problem Solving / Root Cause Analysis \" Strong individual contributor \" Collaborative team player \" Fast and continuous learner \" Flexible/highly adaptive to continuous changing...
Director, Clinical Science
CAMBRIDGE, MA, UNITED STATES
...on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time. Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, impacting millions of people.Our proprietary Gene Traffic Control platform is a...
Director, Clinical Operations
CAMBRIDGE, MA, UNITED STATES
...on the chromatin regulatory system, which opens and closes the right sections of DNA at the right time. Breakdowns in the chromatin regulatory system lead to a wide range of diseases, including cancer, impacting millions of people.Our proprietary Gene Traffic Control platform is a...
Technical Validation Business Systems Analyst
CAMBRIDGE, MA, UNITED STATES
...ensure compliance with regulatory requirements. Provide technical expertise and guidance to project teams regarding validation requirements and best practices. Perform periodic review and revalidation of systems to ensure continued compliance. Stay up to date with industry trends and...
Validation Engineer
CAMBRIDGE, MA, UNITED STATES
...ensure compliance with regulatory requirements Provide technical expertise and guidance to project teams regarding validation requirements and best practices Perform periodic review and revalidation of systems to ensure continued compliance Stay up-to-date with industry trends and...
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