better Biotech Pharma Job in Connecticut

My client a medium size biopharmaceutical company is looking for an In House CRA. The CRA is assist in the preparation for an NDA submission. This position involves the ability to recognize and locate study related ICH essential documents within the company's document management system and in official paper files. My client is looking for someone who is familiar with data management and or statistical documents and data would be a plus. Knowledgeable with FDA/GCP/ICH guidelines and phase 1-3 clinical trial

in Newton Massachusetts and operations in Texas Connecticut RTP North Carolina the UK France and...

My client a medium size biopharmaceutical company is looking for an In House CRA. The CRA is assist in the preparation for an NDA submission. This position involves the ability to recognize and locate study related ICH essential documents within the company's document management system and in official paper files. My client is looking for someone who is familiar with data management and or statistical documents and data would be a plus. Knowledgeable with FDA/GCP/ICH guidelines and phase 1-3 clinical trial

Original Posting Date 01-Nov-2008 STARS Req ID 6275BR Department Psychology University Generic Title Biostatistician Posting Position Title Biostatistician 1 Bargaining Unit None Job Category Managerial & Professional Type of Employment Full Time Duration Type Fixed If Fixed Duration, Period 1 year from date of hire If Fixed Duration, is continuation possible? Yes Salary Grade(Min/Max) 23 Work Week Standard - 37.5 hrs (M-F, 8:30-5:00) Work Location Central Campus Worksite Address 309 Edwards Street Position

Original Posting Date 05-Sep-2008 STARS Req ID 5645BR Department Biotechnology Services University Generic Title Biostatistician Bargaining Unit None Job Category Managerial & Professional Type of Employment Full Time Duration Type Fixed If Fixed Duration, Period 1 year from date of hire If Fixed Duration, is continuation possible? Yes Salary Grade(Min/Max) 23 Work Week Standard - 37.5 hrs (M-F, 8:30-5:00) Work Location Medical School Campus Worksite Address 300 George Street Position General Purpose Provide

City North Haven State CT Job Title MGR CLINICAL DATA 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

City North Haven State CT Job Title CLINICAL RESEARCH ASSOC II Description The incumbent will be empowered to incorporate the Total Quality philosophy into all aspects of the job. This includes working as a team member, striving to meet and exceed external and internal customer expectations and committing to continuous quality improvement. The Clinical Research Associate is responsible for providing clinical guidance, strategy, and support for the development of new technologies, new products, extended product

Clinical Research Associate CRA Senior CRA Connecticut 0805941 Apply Online Description The Clinical Development...Profile Locations USA Connecticut Organization USA02 US Clinical Development Svcs...

Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! Supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal and communication

Keywords clinical pharmacist pharmacy residency specialist pediatric surgical ICU intensive care staff hospital oncology IV SICU Connecticut CT...

Job Advertised by HOSPITAL JOBS ONLINE- STAFF PHARMACIST JOB DESCRIPTION Description: The Staff Pharmacist position, provides pharmaceutical care services to the patients of the hospital including, but not limited to oversight, monitoring, preparation, dispensing and proper documentation of patient medication therapy as well as providing drug information, patient information and oversight of information and dispensing systems. The successful candidate will work with the team to ensure compliance with

Consults with nursing and medical staff on prescription orders, patient reactions, and errors or complaints and conducts drug utilization reviews and prepares drug review criteria for medical staff approval. Requires PharmD degree..POSITION SUMMARY: Support clinical program managers on operation and development of pharmacy clinical management programs using both traditional utilization management (e.g., step therapy, therapy over time, prior authorization) and consumer oriented (e.g., education and incentives

This position is responsible for the statistical support of drug development programs from preclinical to regulatory submission. The major area of responsibility will include the design, analysis and reporting of the series of clinical studies required by these programs. Other activities include providing statistical consultation for the preclinical and drug discovery projects within the company. Interact with project team to plan and identify goals for individual drug development programs. Work with

Our client, a biopharmaceutical company, located in the Central Southern region of CT has an opening for a Supervising Statistician/Biostatistician in the Pharmaceutical Service and Data Analysis Department. The staffing expansion is required to support several specific projects. These projects involve tissue microarray and attendant analytic processes in the field of tissue biomarkers. The work will be under the direction of a senior science team which is recognized as pioneering the commercial development

Our client, a biopharmaceutical company, located in the Central Southern region of CT has an opening for a Statistician/Biostatistician in the Pharmaceutical Service and Data Analysis Department. The staffing expansion is required to support several specific department projects. These projects involve tissue microarray and attendant analytic processes in the field of tissue biomarkers. The work will be under the direction of a senior science team which is recognized as pioneering the commercial development and

Our client, a biopharmaceutical company, located in the Central Southern region of CT has an opening for a Supervising Statistician/Biostatistician in the Pharmaceutical Service and Data Analysis Department. The staffing expansion is required to support several specific projects. These projects involve tissue microarray and attendant analytic processes in the field of tissue biomarkers. The work will be under the direction of a senior science team which is recognized as pioneering the commercial development

Our client, a biopharmaceutical company, located in the Central Southern region of CT has an opening for a Statistician/Biostatistician in the Pharmaceutical Service and Data Analysis Department. The staffing expansion is required to support several specific department projects. These projects involve tissue microarray and attendant analytic processes in the field of tissue biomarkers. The work will be under the direction of a senior science team which is recognized as pioneering the commercial development and

Consults with nursing and medical staff on prescription orders, patient reactions, and errors or complaints and conducts drug utilization reviews and prepares drug review criteria for medical staff approval. Requires PharmD degree..POSITION SUMMARY: Support clinical program managers on operation and development of pharmacy clinical management programs using both traditional utilization management (e.g., step therapy, therapy over time, prior authorization) and consumer oriented (e.g., education and incentives

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 review, preparation for entry, query processing, discrepancy management

Responsibilities: Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! Supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal

Experienced Regional Clinical Research Associates are being sought for one of the top large pharmaceutical companies in the world! Supporting new drug applications, the Regional CRA monitors clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines, and company SOPs. As specified in the monitoring plans, you will support project teams in the placement, implementation, evaluation, and conclusion of clinical studies. This role lets you use your exceptional interpersonal and communication

Description The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your career soar! We are seeking an enthusiastic CRA to join the team in our Northeast region.

Our client is a small pharmaceutical company that needs an experienced Data Manager that can work on a growing team. This is a unique opportunity to work on a 'best of class' drug, finalize work for an FDA submission, and assist in developing a team. With excellent funding, this is a great opportunity to made significant impact on a small, growing company. For confidential consideration, please respond electronically noting the job title and refID in the subject line.. Job Requirements: The candidate must

Clinical Research Associate CRA to Assist in New Drug Application Submission JOB DESCRIPTION - Recognize and locate study related ICH (International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use) essential documents within the Document Management System and in Official Paper Files. (May also involve the search for misplaced documents, if contract time permits which will involve working with company staff to locate documents that may be stored

This contract, in-house CRA position will assist in preparation for an NDA submission. The position involves the ability to recognize and locate study related ICH essential documents within the company's document management system and in official paper files. Additionally the contract CRA will assist in the verification that procedural-related documentation is present and accounted for. The position may involve the search for misplaced documents, if contract time permits which will involve working with company

Clinical Research Associate CRA to Assist in New Drug Application Submission REQUIRED SKILLS - Excellent understanding of clinical research, submission documents, regulations and demonstrated competence in FDA/GCP/ICH guidelines. - Phase 1-3 clinical trial monitoring - Command of medical terminology and of the application of scientific/medical & clinical concepts used to conduct Phase I-IV clinical trials - Ability to work effectively with minimal supervision - Communication skills (both verbal and

POSITION SUMMARY: Support clinical program managers on operation and development of pharmacy clinical management programs using both traditional utilization management (e.g., step therapy, therapy over time, prior authorization) and consumer oriented (e.g., education and incentives) strategies that lead to CIGNA's goal of establishing a meaningful cost advantage and superior clinical outcome. RESPONSIBILITIES Maintain operational efficiency of existing clinical programs Support development of pharmacy

Must be licensed in the state of Connecticut or have reciprocal licensure in order to...

Keywords clinical pharmacist pharmacy residency specialist pediatric surgical ICU intensive care staff hospital oncology IV SICU Connecticut CT...

Welcome to Genesis HealthCare! We're setting the standard for clinical excellence and responsiveness in meeting the unique needs of every resident and patient in our care. We're focused on becoming the recognized leader in clinical quality and customer satisfaction in every market we serve. Position Description: This is a floater position for CT in the New Haven , Wallingford, etc area. The Clinical Operations Manager provides clinical leadership to Center staff and works in collaboration with the Regional

Our customer, an internationally known Sponsor company committed to excellence for all patients, is seeking two clinical data managers to join their team; one for a long term project and the other as a permanent employee. Our customer offers an exceptional work environment, the opportunity to advance as a consultant and employee and benefits that are second to none in the industry. If you re looking to be part of a company that values its employees and offers a fun and friendly work environment than look no

Senior Clinical Data Manager Our client is a small pharmaceutical company that needs an experienced Data Manager that can work on a growing team. This is a unique opportunity to work on a 'best of class' drug, finalize work for an FDA submission, and assist in developing a team. With excellent funding, this is a great opportunity to made significant impact on a small, growing company.

Air Products Healthcare, one of the top five providers of home respiratory products and services in the U.S. and a subsidiary of Air Products and Chemicals, Inc.(NYSE:APD), is seeking a Clinical Pharmacist in our Stratford, CT location. Job Description: The Clinical Pharmacist will perform specified distributive and clinical pharmacy activities and related services as they pertain to providing safe and effective home infusion therapies. Job Responsibilities: -Assists the physician and nursing staff

Our Culture In a world where business is driven by short term financial goals, Boehringer Ingelheim Corporation is truly a company with a different philosophy. Although we are one of the largest and fastest growing pharmaceutical companies in the world, we have been able to maintain a dedication to our values. Our focus is on helping patients, serving our customers and improving the quality of life for the millions of people who rely on us. Simply put, we have remained committed to doing the right thing-for

Our Culture In a world where business is driven by short term financial goals, Boehringer Ingelheim Corporation is truly a company with a different philosophy. Although we are one of the largest and fastest growing pharmaceutical companies in the world, we have been able to maintain a dedication to our values. Our focus is on helping patients, serving our customers and improving the quality of life for the millions of people who rely on us. Simply put, we have remained committed to doing the right thing-for

Our Culture In a world where business is driven by short term financial goals, Boehringer Ingelheim Corporation is truly a company with a different philosophy. Although we are one of the largest and fastest growing pharmaceutical companies in the world, we have been able to maintain a dedication to our values. Our focus is on helping patients, serving our customers and improving the quality of life for the millions of people who rely on us. Simply put, we have remained committed to doing the right thing-for

The incumbent will be empowered to incorporate the Total Quality philosophy into all aspects of the job. This includes working as a team member, striving to meet and exceed external and internal customer expectations and committing to continuous quality improvement. The Clinical Research Associate 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. This may

Accountabilities have an immediate opening for a Clinical Data Manager to support Pharmaceutical industry in Stamford. CT. Candidate will assist in preparation for an NDA submission. The position involves the ability to recognize and locate study related documents and data within the company s document management system, in official paper files and in electronic directories. Additionally The position requires acute analytical skills to determine if all required documents are present and appropriate. Any deviations

in the Pharmaceutical industry and located in Connecticut has an exciting long term contract opportunity...

Qualifications - Prefer BS/BA. - 1 year monitoring experience or combination of on-site monitoring and clinical research coordinator experience. - Customer service orientation. - Sound knowledge of medical terminology and clinical monitoring process. - In depth therapeutic and protocol knowledge as provided in company training. - Ability to perform regionalized travel an average of 65%, depending on project needs. - Excellent verbal and written communications skills.

Job Description To formally apply to this position please visit our website at www.pfizer.com/careers, and reference job requisition # 077744. The Study Manager is responsible for simultaneous delivery of the operational aspects of a number of clinical studies from protocol feasibility through database release. The Study Manager also contributes beyond database release to support effective study reporting and close-out; submission activities; and audits/inspections, as appropriate. The Study Manager

Location: 352 Knotter Drive Cheshire, CT 06410 www.alxn.com recruit@alxn.com fax: 203-699-9940 Responsibility: The primary focus of this position will be to perform a variety of complex and responsible tasks to enter, process, review and validate clinical trial data received in-house and remotely in order to ensure complete, accurate, high quality, regulatory compliant data in support of publications and regulatory submissions. Principal Activities: Develop data entry