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- Pasadena, CA
new job!

The Clinical Trial Data Analyst is responsible for building programs to create datasets, listings, tables and figures from clinical databases, external data sources, and other sources. In addition, the position coordinates in-house data management activities (including vendor management) to ensure the accuracy and consistency of clinical databases for subsequent analysis and reporting. Responsibilities: Prepare data reports, tables and graphs for regulatory submissions, IRB submissions,....

- Sacramento, CA
new job!

Requirements:B.S. Engineering Degree, experienced non-degree acceptable5+ years’ of production floor supervision experiencePluses would be experience out of pharmaceuticals, foods or specialty chemicals and union experienceJob Description: Our client is an expanding player within the pharmaceutical industry. This person will work in a 400-person active pharmaceutical ingredients (API) manufacturing facility. This site runs on a 12-hour shift schedule and in this role, this person will....


Our client is a world leader in laboratory equipment and services, and has an opportunity for a Sales Representative for its industry leading analytical instrumentation used in R&D laboratories. This position will be covering most of Virginia and parts of West Virginia from the Richmond area. Responsibilities:The Technical Sales Representative will be responsible for direct sales of analytical instrumentation products and services (measuring density & viscosity) to R&D customers in

- Manhattan, NY
new job!

Position Summary: Calling on department heads, physicians, nurses, case managers, discharge planners and other healthcare professionals in the hospital and clinical settings to facilitate patient discharge for hi-tech infusion home care services. Requires excellent written and verbal customer service skills and advanced computer skills to interact with sales and operations team members and referral sources. This position is field based and requires daily travel to designated hospital and....


We are looking for a Quality Assurance Specialist who will be responsible for the daily Quality Assurance support in the Manufacturing and Packaging process on site. They will be required to review all appropriate documents during the production process. In this role, the QA Specialist will be readily available to support the Quality Department and the production process; therefore, this position requires the QA Specialist to be flexible based on business need to support QA and business....

- Lancaster, SC

We are looking for a Photographer & Videographer who will be responsible for photography and video services to support company sales and marketing efforts. General Responsibilities:Take high quality photographs and edit the images as neededWork closely with Marketing team to determine video requirements and produce video footage accordinglyHelps set photo and video standards for brands and products in a brand with the ability to brainstorm with members of the Graphic Design / Marketing....


Los Angeles, CA Currently looking for an experienced Manager, Regulatory Affairs - CMC to fill an opening with a Fortune 100 Pharmaceutical Company located in Los Angeles, CA. Interested candidates should hold a Bachelor’s Degree (Regulatory Affairs, Life Sciences, or Engineering) and have 6+ years’ regulatory and/or compliance experience. Responsibilities of the Manager, Regulatory Affairs - CMC Responsible for generation of the region-specific regulatory documents Clinical Trial....

- Chicago, IL

$25B Pharmaceutical Company—North Chicago—Salary Commensurate with Experience The SizzleCompany offers great work/life balance.Company offers competitive benefits and perks, including insurance, PTO and sick days, and work flexibility.Company prides itself on having a diverse and inclusive culture. Note from the Hiring ManagerWill provide relocation assistance for the right candidate.Will sponsor an existing H1B. Position Summary Seeking a Senior IT Auditor to be responsible for conducting....


Location: San Diego, CA Employment Type: Permanent Context: Our client ss is seeking a Sr. Project Manager to manage research and drug discovery projects from the research/discovery phase through to early clinical development. Preference will be given to candidates who have experience with small molecule therapeutics. The ideal candidate will be an innovative, highly motivated project manager with a strong scientific background in preclinical drug discovery research and project management. The


This full time, permanent Mechanical Project Engineer career opportunity is at a company that sets the industry quality standard. They design and build all their products in the United States. The engineers are known for being highly skilled and innovative. Projects are very diverse so the work here is interesting. Employees leave at 3:00 p.m. on Fridays. The successful candidate's duties and responsibilities will encompass:Analyzing and evaluating assigned projectsAssigning and giving....


Associate Director Patient Safety and Loss Prevention | RN or Clinical | New York, NY Competitive Compensation | World-Class Benefits | Exceptional Work/Life Balance Nurse & Clinical Professionals with Patient Safety / Risk Management, Quality or Medical Malpractice Credentials Highly Encouraged to Apply There has never been a better time to leverage your experience and passion for quality healthcare. Make your move from a clinical setting to the corporate world by joining a company that....


Director of Patient Safety and Loss Prevention | New York, NY (Clinical Professionals & Executives) Must live within daily commuting distance to Lower Manhattan Desired Traits: Strategic Thinker | Leader | Ambassador | Liaison | Consensus Builder | Facilitator | Communicator | Analytical Subject Matter Expert | Mentor | Coach | Educator Benefits/Perks: Career Development | Professional Challenge | Career Security | Pro-Active versus Re-Active Work Environment | Partner with a Pedigree....

- Cincinnati, OH

General Description:The QC Analyst IV will join chemistry group to provide technical coaching, perform analytical testing, instrument qualification as required to meet QC cycle times following cGMP. Responsibilities will also include reviewing, reporting test results and ensuring that all activities within the laboratory are performed in compliance with cGMP, internal written procedures and policies. The analyst IV will answer questions that arise regarding cGMP and internal requirements of a....


Three Medical Directors needed The Medical Director is a board-certified physician who has a history of clinical practice, and has significant experience in the cardio therapeutic area, Endocrinology or Renal, Nephrology therapeutic areas. The Medical Director is knowledgeable of the actions of regulatory bodies, in particular FDA, and has experience in clinical trials. An ideal candidate should have significant experience in renal cardio disease management and would thrive on proactively....


Leading Global Pharmaceutical company with office in Waltham Massachusetts Manager, Health Economics & Outcomes Research (HEOR) Position Summary: The Manager for Health Economics & Outcomes Research (HEOR), will be responsible for supporting HEOR activities for company's products. This individual will contribute to evidence generation, development of strategy, data analysis and dissemination and support the HEOR Senior team members (Directors, Senior Directors).....


GLOBAL PHARMACEUTICAL COMPANY IS HIRING A HEAD OF MEDICAL AFFAIRS FOR RENAL Renal Cardio Medical Head (Executive Director) The Renal Cardio Medical Head is a member of the Renal-Cardio Therapeutic Area (RCTA) leadership team and leads the Renal Cardio Core Medical Team. The position can be either a Senior Director or Executive Director based upon the individual's experience. The Medical Lead is knowledgeable of the actions of regulatory bodies, in particular, knowledge of the FDA. He/She has....


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....

- Bridgewater, NJ

The CTM will work closely with the Director, Clinical Operations and Clinical Development team on the design, execution and oversight of clinical trials (all clinical phases) related to pharmaceutical product development and registration. The CTM is responsible for the overall operational planning and activities for the implementation and conduct of studies (clinical trials, IIT studies, compassionate use and registries) including data management activities, ensuring that clinical studies are....


Position Overview Provide analytical expertise and leadership in the development of drug substances and pharmaceutical products from early development through commercialization. Plan analytical research and development activities, devise strategies for achieving project goals and independently manage CMC timelines. Make pivotal contributions to drug product development strategy at project team level. Independently manage multiple projects and ensure timely delivery of all deliverables to meet....


Represents Regulatory Affairs for pharmaceutical development projects and marketed products. Responsible for development and communication of all aspects of global regulatory strategy on R&D project teams. Leads team of regulatory professionals to assure successful planning and completion of regulatory activities on a worldwide basis. Responsible for knowledge of regulatory requirements of major regions (e.g. US, EU JP) with responsibility for working with colleagues on a worldwide basis....

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Unless noted above, applicants MUST be authorized to work in the US without Visa Sponsorship. US citizens and Green Card holders ONLY. We do not provide relocation assistance for those living outside the continental US. Please only click apply if you meet the specific requirements of the job listing, you are able to work in the location listed, and are comfortable with the salary range indicated above. Thanks for your interest. We look forward to working with you.