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Judge healthcare is currently seeking a Proofreader of Global Labeling Delivery in Gaithersburg MD. This position is responsible for primarily proofreading new and revised printed labeling for assigned products. This job will have the following responsibilities: Assist with labeling submissions for US and EU: QC, proofing, copy editing and formatting Assist GRAPSQA labeling operations staff in...
Job Description: JReview Developer will work closely with business groups and provide custom reporting solutions using the JReview clinical business intelligence platform. JReview Developers will provide report specifications development, testing, deployment, and training. JReview Developers will work with project teams to ensure that all client work has met or exceeded client expectations. Key ...
The Clinical Document Specialist is responsible for the management of clinical study records (e.g., clinical Trial Master File) from set-up through to final archival, ensuring compliance with company SOP's and processes. With a focus on inspection readiness, monitors Trial Master File (TMF) compliance and supports preparation of documentation required for regulatory agency inspection and internal...
Global Feasibility Manager Type: Full-Time Office Based Location: Houston, TX About Pharm-Olam International: Pharm-Olam International is a mid-size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of this and more. We are a company that strives to deliver cost-effective, quick-to-market clinical services in...
Opus Scientific is seeking an experienced Senior Project Manager to lead a team in the life sciences industry. Excellent benefits at this cutting edge company! Responsibilities · Professionally lead and manage the setup of multiple clinical trials, including preparation of study specific setup documents and manuals in collaboration with the setup team and other departments on the external and in...
Summary: Reports to the Director, Clinical Development and supports various activities within Clinical Development, including: Content development and review of Protocols, ICFs, and CSRs . Manage and conduct clinical data review and protocol devation review/evaluation. Author Clinical sections of regulatory documents (IND annual reports/DSUR/PSUR, briefing books, etc.). Manage clinical progra...
Our client in the Fremont Area is looking for a QC Associate I to join their team! Duties: Coordination of Quality Control data and handling of Raw Material samples. Ensures that all data is organized and archived per appropriate workflows and SOPs. Works with GMP and non-GMP databases to ensure all samples are received, logged, stored, distributed and tracked within defined timelines. Intera...
The H-J Family of Companies is a growing and innovative manufacturer and distributor of electrical componentsfor power distribution. H-J has built our company on the quality of our products and service. We are looking for a great candidate to join our team as a R&D Engineer. Summary: We are seeking a creative, energetic individual for an R&D engineering position. Essential Duties and Responsibil...
Company Our client is a Dairy Food Manufacturer with an operating facility in the Dayton / Columbus, Ohio region. Your Role with the company: Responsible for the administration, strategy and technical direction of the R&D group on site Providing necessary technical support to vendors, clients, and operations when problems occur with products Communication with both internal and external clien...
If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International (POI) has one of the largest global footp...
Locations: We are seeking a Proposal Development Coordinator/Writer to work on a full-time basis in one of our offices located in Houston, TX / Research Triangle Park, NC / Plainsboro, NJ / Mississauga, Ontario Canada or it can be home based/remote. About Pharm-Olam International If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive glob...
If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International (POI) has one of the largest global footp...
Job Number: 435896 Clinical Trial Lead-Oncology Overview: A Clinical Trial Lead (CTL) is a member of the project team responsible for the execution of the clinical trial(s) at the site level, accountable for development and execution of the clinical monitoring plan (CMP), site identification and selection, CRA and site training, development of CRA and site materials, trackers, and logs necessar...
PROGRAM/PROJECT MANAGER WITH CLINICAL DEVELOPMENT REQUIREMENT #16-00258 RECRUITER: ANNIE DOYLE JOB LOCATION: JERSEY CITY, NJ FEBRUARY 11, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Reports to the Director, Clinical Development and supports various activities within Clinical Development, including: Content development and review of Protocols, I...
JOB SUMMARY: Responsible for organizing and managing the Quality Control Microbiology Laboratory and assuring that Microbiology Lab operations and testing are performed in compliance with applicable regulations, company specifications, procedures, and policies and current industry practices. The position is also responsible for leadership in all microbiological aspects relevant to manufacturing o...
We have an immediate FT Permanent position for a “ Senior Manager - SAS Programming” with our direct client (Top Pharmaceutical Services Company), if you are interested please send your updated resume to resume@ collabinfo.com or please call 609-662-0262. Title: Senior Manager, SAS Programming Location : Madison, WI FT Permanent - Onsite Job responsibilities and duties may include: • Manage a...
We have an immediate position for a “eTMF Specialist” with our top pharmaceutical client, if you are interested please send your updated resume to greg @ collabinfo.com orcall me at 732-788-3483 Title: eTMF Specialist Duration: 8+ Months Location: Princeton, NJ Essential Job Duties: · Function as Designated Project Team Member to whom a lead data manager may delegate eTMF-related tasks. · Sc...
At Joulé, you could say the right match is in our DNA. We're the specialists in Scientific Staffing. Our unmatched industry network and geographic reach enable us to place professionals like you at top firms every day. For more than 20 years, we've been providing temporary, contract and direct staff to pharmaceutical, biotechnology, food, flavor and fragrance, specialty chemical and other scientif...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders R&D Project Manager Apply Opelousas, LA Full-Time $100,000 - $120,000 Job Details We are a prestigious and leading National Food Product manufacturing and distribution company. Currently were have an R&D Project Manager to join our Culinary Technical Services/Research and Development Team. Our ideal candid...
ASSOCIATE CLINICAL SCIENTIST REQUIREMENT #16-00173 RECRUITER: MEGAN STRAWN JOB LOCATION: HOPEWELL, NJ JANUARY 28, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: We are seeking a Research Scientist with knowledge and background in molecular biology to develop, validate and test molecular assays in clinical trial samples. Members of the Clinical Mole...