Biotech Jobs in King of Prussia, Pennsylvania

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155 King of Prussia, PA Biotech jobs found on Monster.

Jobs 1 to 20 of 155
Senior Medical Writer Experience: • A minimum of 5 years medical writing experience within the biopharmaceutical industry or a contract research organization. • A solid understanding of the clinical development process, including the documents that are required at each stage. • Excellent written and verbal communication skills. • Excellent level of English language proficiency. • Expert MS Office...
Job Description: CTMS Business Analyst Consultant We are recruiting on an open ended contract position on behalf of a leading pharmaceutical company looking to expand their Clinical Development Operations and Biometrics team by adding a CTMS Business Analyst. The selected individual will serve as an integral part of the team supporting the Clinical Trial Management System (CTMS), including designi...
SENIOR PROJECT BIOSTATISTICIAN *These remote opportunities are open to any US home-office location. Theorem Clinical Research is seeking Senior Project Biostatisticians for full-time, salaried roles in the US. In this role, the selected candidate will analyze all parts of any clinical study, and provide planning on multiple clinical studies from multiple clients, along with the following: Manage B...
SENIOR SAS PROGRAMMER *These remote opportunities are open to any US home-office location. Theorem Clinical Research is seeking Senior SAS Programmers for full-time positions supporting our sponsor’s biometrics project needs. In this role, the SAS programmer should be able to produce basic analysis displays and information from the clinical data management database and program all tables, listings...
PRINCIPAL SDTM PROGRAMMER *This remote opportunity is open to any US home-office location. Theorem Clinical Research is currently searching for experienced SDTM Programmers. In this role, the SDTM Programmer will be responsible for mapping entire studies in accordance with SDTM guidelines, as well as performing Quality Control checks. RESPONSIBILITIES: Create SAS datasets of clinical data from cli...
Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...
Worldwide Clinical Trials (WCT) is a leading therapeutically focused Contract Research Organization (CRO) that applies deep therapeutic expertise to help customers achieve their drug development goals. WCT’s global footprint, full complement of development service offerings, and innovative use of proprietary and cutting edge technology, bring about an environment which allows us to focus on identi...
Company Confidential King of Prussia, PA, 19406
Title of Position: Regulatory Affairs Associate (Biologics/Vaccines) Job Description: The scope of the work is to assist CMC Regulatory Affairs personnel by representing RA in project team meetings, assessing the content requirements for IND amendments or BLA supplements, assisting in the draft, review and/or editing of regulatory submissions, taking responsibility for review and quality of publis...
Start: immediately, upon background check process completion Duration: five months/role could extend and/or become permanent Location: Wayne, PA 19087 DESCRIPTION This role is responsible for working individually or within a team of analysts and/or projects to improve and maintain business processes within various teams. Basic Qualifications A four-year degree, or the equivalent in work experience...
Global provider of business and consumer finance solutions seeks Data Analyst with expertise in data mining and reporting using SPSS, SQL, and Excel. •Developing data queries for reporting, ensuring high data quality and accurate information to support scorecard management and other stakeholders. •Analyzing large datasets and preparing reports. Presenting this analysis (directly or indirectly) to...
Project Support Specialist-Clinical Site Regulatory Document Management Location: Audubon, PA Duration: 6-months Requirements: - BS Degree Preferred - 6 months of experience supporting site initiation and activation by collecting an maintaining essential regulatory documents (1572’s, informed consent forms, investigator CV’s) - Experience working with electronic document management systems preferr...
Requirements: - BS in Biology or Healthcare field - 1 year experience in Drug Development, Regulatory Affairs, CRA experience a plus. - Dialysis, Rheumatology, Oncology, Cardiology, Pediatrics or GI experience preferred - Ability to travel up to 80%, including overnight - Knowledge of Medical/Regulatory Terminology Description: - Assist with Administration of clinical research projects: recruiting...
Job Description Research Scientist is responsible for developing new algorithm capabilities in support of non-traditional ISR techniques. This position will be hired for Valley Forge, PA; a TDY to Goodyear, AZ may be required until the program completes relocation transition (late summer 2014). Applicants selected will be subject to a government security investigation and must meet eligibility req...
Nature and Scope The Regulatory Associate provides administrative support to the Clinical Regulatory group. He/She is responsible for the organization and compilation of the regulatory submissions and maintains the regulatory files to ensure that dossiers are easily retrieved for review by the team. He/She works with pharmacovigilance to process and file Pharmacovigilance reports to the FDA in a t...
ePharmaSolutions (ePS) is a global industry-leading clinical services and technology solutions provider that supports the top pharmaceutical, biopharmaceutical and clinical research companies in the world. Our award-winning Clinical Trial Portal (CTP) and eTMF are used by more than 350,000 clinical researchers in 135 countries. At ePharmaSolutions, we welcome your knowledge, experience and enthusi...
ePharmaSolutions (ePS) is a global industry-leading clinical services and technology solutions provider that supports the top pharmaceutical, biopharmaceutical and clinical research companies in the world. Our award-winning Clinical Trial Portal (CTP) and eTMF are used by more than 350,000 clinical researchers in 135 countries. At ePharmaSolutions, we welcome your knowledge, experience and enthusi...
PLYMOUTH MEETING, 19462
As an Army National Guard Chemical Operations Specialist, you'll be there and prepared whenever a community is flooded, an earthquake shakes the foundations of a city, a hurricane makes landfall, or an enemy uses biological or chemical warfare. You will know what to do to evacuate the area, control the situation, and solve the problem. In order to perform these functions, you will be trained to ex...
Staffing Sales Account Executive: At Workforce Integration - Wi? - we know people are the key to successful organizations. So we have concentrated on getting people down to a Science. Ask us Wi? We are currently seeking a Staffing Sales Account Executive to work out of the Greater Philadelphia ares. This role is critical to our company's continued success. Major Duties and Responsibilities: As a s...
ePharmaSolutions (ePS) is a global industry-leading clinical services and technology solutions provider that supports the top pharmaceutical, biopharmaceutical and clinical research companies in the world. Our award-winning Clinical Trial Portal (CTP) and eTMF are used by more than 350,000 clinical researchers in 135 countries. At ePharmaSolutions, we welcome your knowledge, experience and enthusi...
Overview This is an experienced Ph.D. level position requiring the individual to have laboratory expertise in synthetic organic chemistry. This position requires full use and application of chemical principles, theories and techniques applied toward a wide range of difficult problems across projects within one or more areas of expertise. The individual will be responsible for conduct, evaluation a...
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