Fulfill role as primary preceptor for University of Connecticut School of Pharmacy Infectious Disease Clinical Rotation program...have current Pharmacist license in State of Connecticut or be eligible Ability to communicate effectively...
BASIC PURPOSE - Perform duties of a Trial Statistician to support trials within national or international development projects or for marketed products as required. - Assure well-designed clinical trials. - Provide statistical expertise necessary to support the design as well as analyze, interpret and communicate the results of clinical trials. - Support other Trial Statisticians in their responsibilities. - Support Project Statisticians in their responsibilities, especially in their statistical
At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you
At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you
City NORTH HAVEN State CT Job Title CLINICAL RESEARCH ASSOC II Description SUMMARY OF POSITION: Participates in clinical research programs by assisting with the development of study protocols, case report forms, clinical reports, performing site monitoring visits, and interfacing with site coordinators, field clinical staff, and other company representatives. ESSENTIAL FUNCTIONS: . Ensure that documentation from investigators and investigational sites meets FDA/GCP/ICH requirements. . Assist in designing, planning
Clinical Data Manager Our client, a Successful and Thriving Medical Device company, has an opening for a Clinical Data Manager. The Clinical Data Manager is a lead member of the clinical research team responsible for data management activities across multiple trials. Activities include assisting in data entry, query processing, site management, data reporting and other data management activities in support of clinical trial projects. Perform data management activities on both paper based and Electronic data
City North Haven State CT Job Title Clinical Data Manager Description SUMMARY OF POSITION: Member of clinical research team responsible for data management activities across multiple trials. Activities include assisting in data entry, query processing, site management, data reporting and other data management activities in support of clinical trial projects. ESSENTIAL FUNCTIONS: Perform data management activities on both paper based and Electronic data capture (EDC) studies. Major activities include: .CRF data
Connecticut Children's Medical Center|Hartford, CT|
a full service pediatric hospital in Hartford Connecticut currently has full and part time positions...Connecticut Children s Medical Center CCMC a full...Department Pharmacy General Schedule Full Time Facility Connecticut Children s Medical Center Main Campus Shift...
Job Description The responsible person will serve as safety lead on assigned clinical study teams and will contribute to the development of study-related documents as well as the review and analysis of safety information. This individual will be responsible for ongoing review of accumulated safety data and assist in the development and maintenance of accurate risk profiles for assigned products. Drug Safety Specialist / Manager Duties and Responsibilities Prepares relevant safety documents for company management
POSITION SUMMARY: Directly responsible for ensuring that adverse events are processed, analyzed and reported according to Corporate SOP's, Local Working Instructions and local regulatory requirements. Responsible for distribution and retrieval of data to internal and external customers as needed for analysis and compliance with regulations. Serve as point of contact with clinical team in areas of adverse event process. DUTIES & RESPONSIBILITIES: - Assists in developing and/or implements customized
Summary This position is responsible for providing onsite pharmacy and health education support for employees/participants who are candidates for, seeking to be, or are already engaged in their organizations health management program. The Onsite Pharmacist Health Advocate will provide one-on-one pharmacy/health education and referrals to employer-sponsored pharmacy/health programs that are available through CIGNA and other community-based resources, as appropriate. Duties/Responsibilities: The Onsite Pharmacist
MedFocus Pharmaceutical Research Opportunities|Wallingford, CT|5-7
R&D BIOSTATISTICS COMPANY INFO: MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device industries. We specialize in the nationwide recruitment of clinical trials personnel. Our client is a leading provider of medicines to fight cancer, cardiovascular and infectious diseases -- including HIV/AIDS -- and serious mental illness and is seeking to add a R&D Biostatistics to their team in Wallingford, CT. RESPONSIBILITIES: Provide
City North Haven State CT Job Title Clinical Research Associate II Description SUMMARY OF POSITION: The Clinical Research Associate II is responsible for providing clinical guidance, strategy and support for the development of new technologies, new products, extended product claims and post-market clinical research and surveillance. ESSENTIAL FUNCTIONS: .Maintain the professional competency, knowledge and skill necessary for the successful performance of assigned duties and responsibilities. .Maintain adequate
SUMMARY OF POSITION: The Clinical Research Associate II is responsible for providing clinical guidance, strategy and support for the development of new technologies, new products, extended product claims and post-market clinical research and surveillance. ESSENTIAL FUNCTIONS: Maintain the professional competency, knowledge and skill necessary for the successful performance of assigned duties and responsibilities. Maintain adequate knowledge and understanding of current scientific literature required to
Original Posting Date 09-Apr-2009 STARS Requisition number 7189BR Department Yale Ctr For Clin Inv University Generic Title Biostatistician Bargaining Unit None Job Category Managerial & Professional Type of Employment Full Time Duration Type Regular (Min/Max)">Salary Grade(Min/Max) (Min/Max)">23 Work Week Standard - 37.5 hrs (M-F, 8:30-5:00) Work Location Medical School Campus Worksite Address 2 Church Street South Position General Purpose Assist faculty from the Yale Center for Clinical Investigation (YCCI