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This position will be in the Labelling Excellence & Operation team within the Global Regulatory Labeling department. The position will be responsible for: Preparation of US labelling documents. Ensuring compliance..
Provide operational support on MS GHEVA plans and activities Ensure alignment with MS product / brand strategies, in close collaboration with matrix teams: V&A leads, Medical, & HEVA team Work..
Subject/Patient recruitment for clinical trials: ? Ability to convey the purpose of the study and eligibility requirements to study volunteers. Becomes familiar with individual protocol/consent details. ? Phone screening of..
Job Title: Clinical Trial Operations Manager III Provides input into identifying implications of study progress on overall timeline goals and conduct plans. Provides input into content and execution of investigator..
Principal Clinical Trial Manager (Contractor) Position Description: The Principal Clinical Trial Manager provides leadership and oversight of the clinical research program(s) to ensure delivery on time, within budget, and of..
The Pharmacovigilance Scientist (PVS) will serve as a core member of the safety team and is responsible for performing proactive pharmacovigilance activities on a product, or group of products in..
Responsible for the collection, data entry, routing, follow-up, and timely reporting/submission of safety information related to drug products from a variety of sources (clinical trial, spontaneous, literature), both U.S. and..
Job Summary: This U.S. Trade Customer Support team member is an integral part of the order to cash process. Trade Analyst shall perform tasks on a daily basis that directly..
This Global Regulatory Affairs (GRA) Labeling Associate position will ensure active adherence to the local and global labeling processes using the appropriate tools and systems to ensure harmonization and compliance..
Duration: 12 months Job Description: System Administrator/System Archive SME for contract work in Peapack, NJ. Responsibilities would include, but are not limited to, administering a Server development room and Data..
This role is not a Data Manager. It's a clinical role and data mangers are not qualified. ? Degree in life sciences ? Experience working on oncology or hematology clinical..
Onsite at Thousand Oaks or Cambridge, MA Peferred: RN, PharmD or PA Clinical/medical research experience Processes and regulations for pharmacovigilance and risk management Aggregate data analysis, interpretation and synthesis Signal..
This is for STATISTICAL Programmer role. Typical Daily Work Hours = 8am to 5pm (some flexibility in start/end times) Weekend work & OT is not required. 100% onsite work. Responsibilities..
Correct title: Consultant Biologics Drug Product Manufacturing The successful candidate will manage the manufacturing and clinical supply chain for a range of therapeutic protein products in clinical development ? Will..
What's Our Competitive Edge? * We aren't the new guys on the block in Consulting, Sales & Marketing! We are local, established and already connected to the community. * Our..
Communications Representative - Full Time Our Company has openings for full time, entry level Customer Service / Marketing Representatives working with our team. This representative will be .....
Entry Level Customer Service & Sales Rep [CSR | Full Time] Looking to join a company who embodies a "Work Hard, Play Hard" philosophy? We thought so. Entry Level Customer..
Blue Square Concepts is seeking brand assistants/marketing coordinators to act as the face of client brands and marketing & sales campaigns throughout the Houston area. Our client creates tailored .....