Biotech Meeting Event Jobs

562 jobs

Meeting Planner Job Label:MAG_14C0AAA0873-2 Meetings and Events International is a state-of-the-art meetings and communication company specializing in the healthcare industry. Since 1984 we have partnered with pharmaceutical, biotech, and medical device companies to provide compliant education to healthcare professionals and patients. Predicated on MEI's extensive industry experience, our soluti...

Meetings and Events International is a state-of-the-art meetings and communication company specializing in the healthcare industry. Since 1984 we have partnered with pharmaceutical, biotech, and medical device companies to provide compliant education to healthcare professionals and patients. Predicated on MEI's extensive industry experience, our solutions are designed to keep pace with your needs,...

Unique chance for a confident Executive Assistant to provide support to a very busy executive and be part of a great team dedicated to making this company succeed. As the Executive Assistant, you will be responsible for providing support including calendar management, frequent travel coordination, arranging meetings and events and screening all calls to the CEO and other senior leaders. Ideally th...

Join Theorem Clinical Research for a SAS Programmer/Statistics Interview Day in Plymouth Meeting on March 18, 2015. SAS PROGRAMMING Statistical Programmer/Analysts Senior Statistical Programmer/Analysts Principal Statistical Programmer/Analysts Manager, Statistical Programming CDISC/SDTM Subject Matter Expert STATISTICS Principal and Analytical Statisticians Manager, Statistics Associate...

Regeneron Pharmaceuticals is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, inc...

Regeneron Pharmaceuticals is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, inc...

Regeneron Pharmaceuticals is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, inc...

Convention Partner, Commercial Meeting & Convention Services Requisition ID-00435655 Description The general purpose of the Convention Partner role is to provide support to the Convention team specifically focused on coordinating assigned housing, registration, ancillary events, maintenance of the convention schedule, collaborating with Meeting Partners on larger convention housing projects, cr...

Drug Safety RN. This is a 4 month contract with our client. This is a remote position. Pay is $35-$41/hr. Here is the job description: RESPONSIBILITIES: Review, assess, and identify safety adverse events from US patient medical records (patient charts), using project-specific instructions. Assess patient records and flag for adverse events. The review must be performed on time, within budget a...

To serve in a supportive capacity to the Clinical Trials Managers/ Clinical Trial Leaders (CTMs/CTLs) for their assigned clinical trials and Field staff (CRAs). Relevant tasks may include collection of regulatory documents, maintenance of various tracking databases, processing of Serious Adverse Event reports, review of trip reports, approval of CRA expenses, and co-monitoring for one or more proj...

Provides high level medical expertise in the safety evaluation and risk management of key company assets or other highly complex products in clinical development and/or the post-marketing setting Ensures that adverse event and other safety information is efficiently evaluated in order to meet global compliance and regulatory requirements, identify the need for product labelling updates and drive ...

Provides high level medical expertise in the safety evaluation and risk management of key company assets or other highly complex products in clinical development and/or the post-marketing setting Ensures that adverse event and other safety information is efficiently evaluated in order to meet global compliance and regulatory requirements, identify the need for product labelling updates and drive ...

The Opportunity: Drug Safety Scientist The Drug Safety Scientist assists and supports the ongoing aggregate review and analysis of product safety for both pre and post-marketing data. Tasks include preparation and authoring of aggregate safety data including signaling analysis, DSUR, PSURs (Periodic Safety Update Reports), Annual Safety Reports, and reports to support internal/external data safet...

The Opportunity: Drug Safety Scientist The Drug Safety Scientist assists and supports the ongoing aggregate review and analysis of product safety for both pre and post-marketing data. Tasks include preparation and authoring of aggregate safety data including signaling analysis, DSUR, PSURs (Periodic Safety Update Reports), Annual Safety Reports, and reports to support internal/external data safet...

**Description:** Thecandidate will work alongside their Senior Analyst and Junior Analyst peers inall aspects, from idea generation to company/medical meetings, including butnot limited to the following: ·Perform complex financial modeling & valuation work. ·Write regular industry and company reports and company launch initiations fromscratch. ·Evaluate medical literature/studies to opine on t...

Essential Responsibilities: -Collection, logging, tracking and filing of essential regulatory documents (TMF filing/coordinating) -Tracks and distributes study specific documents such as operational, pharmacy, and lab manuals to clinical research organization (CRO) and study sites if applicable. -Assist with the management and meeting coordination of the members of our data safety monitoring bo...

Thecandidate will work alongside their Senior Analyst and Junior Analyst peers inall aspects, from idea generation to company/medical meetings, including butnot limited to the following: ·Perform complex financial modeling & valuation work. ·Write regular industry and company reports and company launch initiations fromscratch. ·Evaluate medical literature/studies to opine on therapeutic/marketo...

CRA: Core role is to verify that investigational sites are adhering to the rights and well-being of human subjects, the reported trial data are complete, accurate, and verifiable against source documents, and that the trial is conducted in compliance with the currently approved protocol, Good Clinical Practices, applicable regulations and applicable standard operating procedures (SOPs). Conduct ...

Description Intern, Biotech Innovation and Commercial Strategy Company Summary: Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, cancer, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique ...

Executive Assistant jobs in San Diego, CA Ajilon Professional Staffing is proactively seeking candidates to fill Executive Assistant jobs in San Diego, CA for our clients in the biotech and life sciences industries. Candidates may be responsible for executive assistant, event planning, office management, and personal assistant duties. These opportunities are temporary to direct hire and direct hi...