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We are looking for a Research and Development Technician to assist formulation scientists by conducting lab scale formula trials, analyzing finished goods, reporting results to R & D team assisting production during the scale-up process and maintaining a clean and safe work environment. General Responsibilities:Effectively collaborate and communicate with R & D teamAccurately weigh appropriate raw materials for lab batchesPerform laboratory bench work to investigate formulations and....


Our client is a global leader in the manufacture of coatings and related technologies. They currently require an experienced chemist/material scientist to lead projects and people in order to characterize materials, differentiate product performance and drive product development. This position is located at a corporate research facility in Minneapolis. ResponsibilitiesLead material science research programs in collaboration with business unit R&D teams. Build core technology competencies....


Global Specialty Pharmaceutical company in Bridgewater, New Jersey is looking to hire a Manager of Clinical Quality AssuranceThe Manager Clinical Quality Assurance is a key member of the company Research and Development organization. This role is responsible for Clinical QA activity related to the planning, conduct, and reporting of GCP audits in order to ensure that clinical studies are conducted in compliance with applicable regulations, guidelines and company standards. This role also has....


The Manager, Medical Information will assist in the operational oversight of medical information within the Medical Affairs function under the guidance of the Lead of Medical Information. The manager will be responsible for providing and supporting the provision of accurate, scientifically balanced and timely responses to inquiries received from health care professionals, consumers and other customers. The manager will monitor the scientific literature and communicate new data to relevant....


High Profile Pharmaceutical company with recent FDA one of a kind approval is hiring a Senior Manager of Regulatory Affairs CMC Reporting to the director technical writing of RA CMC of Regulatory Affairs, the Senior Manager of Regulatory Affairs, CMC will be responsible for the preparation of high quality regulatory submission content focusing on CMC to support global clinical development, registration, and product life cycle management in accordance to regulatory requirements and guidelines.....


The Rare Disease Global Regulatory Team Lead (GRTL) is a Director-level role which is part of the Global Regulatory Affairs (GRA) team based in the US. He/she is responsible for developing long- and short-term regulatory strategies that impact company’s business objectives. Specific responsibilities include: Global Regulatory Team Lead (GRTL) is responsible for developing global regulatory strategy for projects in his/her remit, which include both pipeline and life cycle management programs.....


Our client is seeking a strong Field Service / Applications Engineer for their CNC Turning line of Machine Tools. Strong technical skills on Miyano or other Turning CNC Machines. May consider other CNC Machining experience with the right technical background. Strong knowledge of Programming, Process Troubleshooting, installations, maintenance, preventative / predictive maintenance programs, training of personnel, and the ability to work with customers to resolve problems. Required Job....


Our client is seeking a strong Field Service / Applications Engineer for their Swiss CNC line of Machine Tools. Strong technical skills on Citizen or Miyano CNC Machines. May consider other CNC Machining experience with the right technical background. Strong knowledge of Programming, Process Troubleshooting, installations, maintenance, preventative / predictive maintenance programs, training of personnel, and the ability to work with customers to resolve problems. Required Job Functions:....

- Kenosha, WI

Title:- Systems Engineer - Linux Position Responsibilities:- - Design, plan and implement enterprise-wide Unix system solutions. - Support server software and hardware and related applications and systems. - Design systems that proactively monitor health and performance of systems and infrastructure. - Assist in capacity planning, data center build outs and performing software/firmware upgrades. - Implement tools to provide analytic trend analysis and performance data. - Assist in standardized

- Kenosha, WI

Provide support for WAN, LAN and WLAN with a Cisco centric infrastructure, routers, firewalls, security, wireless, LAN switching, Nexus Data Center, along with LAN/WAN design and implementation.Manage load balancing (DNS/DHCP/IP).Provide remote access solution support (VPN, Terminal Services).Perform remote monitoring and management of system alerts and notifications.Run application performance and packet analysis.Work with emerging technologies such as SD-WAN or Data Center products.Manage....


Pharmaceutical company is hiring an Associate Director Medical Writing for their Waltham Massachusetts location.We are a leader in innovative medicines that address the unmet needs and challenges of people living with debilitating diseases. As a fully integrated global biopharmaceutical company, we apply our scientific expertise, proprietary technologies, and global resources to develop products that are designed to make a meaningful difference in the way patients manage their disease. Our....


Top Tier Pharmaceutical company (with focus in Cardio, respiratory, CNS, Psych and more) in Madison, NJ is looking for a new Director, Clinical Development for to add to this growing team!The Director Clinical Development will report directly to the Vice President and is responsible for the scientific, strategic, therapeutic, and operational management of programs to evaluate, register, and market pharmaceutical agents. Lead and direct study programs, activities, and teams for one or more....

- Buffalo, NY

Clinical Project Manager As a Clinical Project Manager (CPM), you will work in a matrix management environment and serve as the primary contact for interdepartmental and external study contacts. This experienced CPM role is responsible for managing all stages of a clinical study within GCP and ICH guidelines when direct management by the sponsor is required. The CPM may also function as the liaison and provide support for sponsor managed studies in an international setting, and, may oversee....


Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study personnel


Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study personnel


Safety Physician POSITION OBJECTIVE: Supports the Pharmacovigilance team in reviewing, querying, documenting and reporting on all serious adverse events (SAE) & Suspected Unexpected Serious Adverse Reactions (SUSAR) cases related to clinical studies. Essential Job Functions/ResponsibilitiesProvide timely and sound medical review of individual case safety reports (ICSR) from clinical trials.Actively participates in the case initiation process (case triage) and case data inputting/data entry

- Cranford, NJ

As a Clinical Study Monitor, you will work within a clinical team setting to ensure study compliance with protocol, FDA and ICH guidelines. Essential Job Functions/Responsibilities · Ensure the Sponsor, Investigator, and study team adhere to current FDA regulations, applicable ICH/GCP guidelines, local policies and standard operating procedures. · Adhere to monitoring plan protocols; e.g. monitoring visit type, frequency, and required critical monitoring activities by utilizing monitoring....

- Buffalo, NY

Senior Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study....

- Cranford, NJ

Senior Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. . Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study....


Clinical Research Physician Global Oncology Pharmaceutical company is expanding and looking to add an MD Strong base salary and benefits and long term incentives POSITION OBJECTIVE: The Clinical Research Physician will be dedicated to providing a leadership role on a matrix team dedicated to stage appropriate clinical development of multiple innovative compounds. He or she will lead the development of clinical strategies for compounds and drive their successful implementation. Essential Job....

161-180 of 238 results