R & D Jobs in Collegeville, Pennsylvania

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144 Collegeville, PA R & D jobs found on Monster.

Jobs 1 to 20 of 144
Bench Scientist Biologist needed for a contract opportunity with Yoh's client located in Collegeville, PA. Top Skills Should You Possess: - Molecular Biology - ELISA What You'll Be Doing: - Provide molecular biology support to R&D therapeutic area program teams on a worldwide basis. - Involves molecular cloning and characterization of cDNAs in support of drug discovery (for generation of recombina...
Job Details: Duration : 12+ Months Contract with possible extension Location : Collegeville, PA 19426 Title : Global Innovative Products Clinical Quality Control Reviewer The candidate will review and modify submission-ready clinical documents by demonstrating high attention to detail, in order to guarantee quality of the final document. The ability to work independently to think through results,...
The candidate must have strong organizational skills and attention to detail . Their background must include technical writing skills, documentation management and technical expertise in the pharmaceutical industry. Position responsibilities: • Facilitate the creation or revision of global Quality Standards. • Collaborate with technical SMEs to ensure that revisions are accurate and consistent wit...
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...
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...
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...
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...
Manages and prioritizes tasks related to data management to meet project needs. Responsible for overall quality of the database to be delivered to the statistician and sponsor. ESSENTIAL FUNCTIONS: Serve as UBC primary contact for data on a project Responsible for delivering quality databases to stakeholders and communicating any clarifications or details that would affect the data analysis to the...
SUMMARY OF POSITION: Responsible for the oversight, management and development of client proposals and pricing for UBC Commercial Services (including REMS with ETASU, Reimbursement, Clinical Call Centers, Nursing Site of Care, and Patient Assistance Programs). Duties consist of a broad range of proposal development activities, including but not limited to the management of the development of mediu...
This is a lead position contributing to functions of the programming roles within the Biostatistics and Programming Departments. Responsibilities include: Acts as the lead programmer on multiple studies Manages project timelines, budgets, and resources Effectively assigns and communicates priorities and work direction to ensure completion of assigned tasks on time and within budget Oversees the pr...
Company Profile: Inovio Pharmaceuticals is a Blue Bell, PA based vaccine product development company with research and engineering facilities in San Diego, CA and Blue Bell, PA. Inovio is developing a new generation of vaccines, DNA vaccines, to treat and prevent cancers and infectious diseases. These SynCon® vaccines are designed to provide broad cross-strain protection against both known and new...
A large and globally renowned Clinical Research Organization is currently recruiting for a Clinical Research Associates (CRA) to join their organization for long term 12+ month contract position on site at their headquarters in Blue Bell, PA. This position is an onsite CRA position with minimal travel interstate to Kansas City, MO. This position is paying a generous hourly rate with the possibilit...
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