THE LARGEST COLLECTION OF PHARMACEUTICAL JOBS ON EARTH
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Our client turns ideas into life changing medicines. They have a very robust pipeline and they focus on breakthrough science. The environment is entrepreneurial, with the goal of making the impossible ..
Position Description / Responsibilities Vedanta is looking for a talented Clinical Trial Associate (CTA) to add to our growing clinical operations team. The candidate will participate in a variety of my ..
Kelly Services is currently seeking au00a0Pharmacovigilance SABR Associateu00a0position withu00a0one of our top pharmaceutical clientsu00a0inu00a0Cambridge, MA for au00a0 W2u00a0contract through the end of 2018.u00a0rnPOSITION SUMMARYu00a0rnrnThe SABR QC PRM Senior Associate II liaise ..
Junior manager sought for a freelance position supporting CDM tasks, entering and verifying data, supporting research trials. Science-focused BA/BS, exceptional communication skills, computer proficiency a must. Long-term, one year, temporary job.
nnJob DescriptionnAt ProClinical, we are seeking an individual to fill the role of Regulatory Associate II and III, based in Raynham, MA.Aid in preparation and submission of global regulatory documents.Provide independent ..
nnJob DescriptionnSABR Senior Associate IIThe Company: A global and well-known biotechnology company located in Massachusetts is seeking to hire a Safety and Benefit Risk Management, Quality and Compliance, Process and Records ..
The CMC Regulatory Affairs Network Strategy Implementation Team Lead will provide leadership and be the Regulatory CMC point of contact for major projects in the Network Strategy Implementation workstream, including ..
nnJob DescriptionnDescription:rrrThe CMC Regulatory Affairs Network Strategy Implementation Team Lead will provide leadership and be the Regulatory CMC point of contact for major projects in the Network Strategy Implementation workstream, including ..
nnJob DescriptionnAt ProClinical, we are seeking an individual to fill the role of Associate Director of Clinical Pharmacology, based in Cambridge, MA. The ideal individual will support drug development by providing ..
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription ..
Rubius is seeking a Research Associate to join the Discovery team to help develop, and advance Red Cell Therapeutic prototypes from idea creation to proof of principle. The candidate ..
The candidate will work as part of a team that provides patient testing to support Sanofi Genzyme's post-marketing commitments in a GCLP and CLIA compliant laboratory environment. The position will focus ..
Job Description :
The Associate Clinical Trial Manager assists the Clinical Trial Managers in the conduct of trials and may be responsible for managing startup activities, vendor communication or other project ..
Will work on reviewing investigational sites and CRO performance deliverables, assisting with selecting and recruiting investigational sites, and performing on-site monitoring. At least 3 yrs of experience is required. Contract position. ..
Full-time, temporary position requiring at least a bachelor's degree. Duties include serving as a team lead for network strategy implementation leads, acting as a point of contact for major projects, & ..
Manage and conduct the monitoring of clinical sites, function as a primary contact and collaborate with projects managers, forms for case reports and procedure manuals. Option for remote job with moderate ..
Associate Director, Immuno-Oncology Research','1800459','!*!
Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. ..
Sound good so far? It really is!
We are inclusive, prize ingenuity, and are united by a common mission to rapidly advance transformative medicines for patients who cannot get ..
SummaryThe Safety Process and Records Management Sr. Associate II will lead and manage Biogen's pharmacovigilance system master files (PSMF). With a strong knowledge of safety regulations and systems, this ..
PURPOSE AND SCOPE : The Clinical Research Associate II (CRA II) supports the companyu2019s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all ..
What you'll be doing
Ensures a consistent and timely completion of launch readiness activities. Provides guidance and develops launch expertise among functions to ensure launch excellence. Works with functions ..
10194BR,ActualValueFromSolar:null},Department Analytical Development ,ActualValueFromSolar:null},Posting location Boston, MA ,ActualValueFromSolar:null},Job Title/Position Title Sr. Scientific Associate,ActualValueFromSolar:null},Posting Job Title Scientific Associate II Analytical Development,ActualValueFromSolar:null},Job Description Vertex is seeking a talented individual to join our Analytical ..
Associate Director, Statistical Programming The Role:
This role is an exciting opportunity to be a critical part of the clinical development group of a high growth organization that is radically ..