Assoc Dir, Medical Communications
(8321BR)
-. Parsippany
Our Strength Is Our People. Passion. Principles. Perspective. At Watson, these are the traits that drive our growth and we apply them to every project and product. If you bring these qualities to your work, then we'd like you to consider joining our team. Watson Pharmaceuticals, one of the world's.
Date posted: 01/28/2012 .
Associate Medical Director - Product Safety
(8472BR)
-. Lake Forest
Provide medical approval and validation of safety reports (as defined by SOP's), including post-market events, clinical events, and periodic reports... Major Duties and Responsibilities:Oversee the process and completion of medical assessment of both drug... Review and evaluate any drug and/or device safety issues and ensure compliance with worldwide regulations and/or...
Date posted: 01/18/2012 .
Marketing Communication Specialist - CF
(3475BR)
-. Cambridge
The Marketing Communication Workflow Specialist coordinates the review and approval of Branded and Non-branded Communications in support of the CF Franchise. Provides support for Communications Review Committee (CRC) Process, including; submission through final approval, production, fulfillment and file archiving. Guide marketing and other key functions through the CRC submission, scheduling.
Date posted: 01/10/2012 .
Product Surv Quality Assoc I
(50857BR)
-. Round Lake
Summary:This position is responsible for complaint handlingEssential Duties and Responsibilities:* Process complaints which may include:* Collect necessary complaint information* Determine reportability of a complaint and submit associated MedWatch reports within 30 days per regulations* Evaluate complaint for need to investigate and coordinate sample retrieval* Document investigation and sample evaluation results*...
Date posted: 01/04/2012 .
Product Surv Quality Assoc I
(50857BR)
-. Round Lake
Summary:This position is responsible for complaint handlingEssential Duties and Responsibilities:* Process complaints which may include:* Collect necessary complaint information* Determine reportability of a complaint and submit associated MedWatch reports within 30 days per regulations* Evaluate complaint for need to investigate and coordinate sample retrieval* Document investigation and sample evaluation results*...
Date posted: 12/29/2011 .
Associate Director, Marketing - Tivozanib
(11-CO126)
-. Cambridge
About AVEOAVEO Pharmaceuticals (NASDAQ: AVEO) integrates a proprietary cancer biology platform with drug development and commercial expertise in its efforts to discover and develop targeted cancer therapeutics. The company's lead product, tivozanib, is an oral, triple VEGF receptor inhibitor with a highly differentiated profile. Tivozanib is currently being investigated in.
Date posted: 12/17/2011 .
Product Surv Quality Assoc II
(49874BR)
-. Round Lake
* Monitor team metrics for critical procedural requirements* Process complaints which may include:* Collect necessary complaint information* Determine reportability of a... Subject matter expert for complaint process. Address first line questions on complaint process. Distribute daily assignments to assigned team. Train and mentor Product Surveillance team. Also responsible for complaint...
Date posted: 12/10/2011 .
Senior Medical Communications Scientist
(3362BR)
-. Cambridge
As a member of the Vertex Pharmaceuticals Medical Affairs group, the Senior Medical Communications Scientist will involve researching, creating, and editing documents associated with Medical Communications and Publications, including manuscripts, abstracts and conference presentations and educational materials... This position will work closely with the Director, Publications and Manager, Publications to.
Date posted: 12/06/2011 .
Sr Mgr/Associate Director, Scientific Communications
(6177)
-. Gaithersburg - Corporate Headquarters
Responsibility for managing the operations of Oncology Scientific Communication Team activities conducted within the Medical Information & Scientific Communications (MISC) department in Medical & Scientific Affairs (MSA) division of the Medical Organization... This person will serve as a key contact for their assigned teams' activities involving Oncology/R&D Strategic Publication Planning.
Date posted: 12/01/2011 .
PV Medical Writer I
(50393BR)
-. Deerfield
The successful candidate will be a member of the Medical Writing team in the Global Pharmacovigilance organization... The Medical Safety Writer is responsible for the coordination, preparation, and completion of Periodic Adverse Drug Reports (PADERs), Periodic Safety Update reports (PSURs), and other ad hoc safety documents for submission to regulatory...
Date posted: 11/19/2011 .
Create job alert using this search criteria
