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- Clearwater/St. Louis, MO, FL

Assistant or Associate Director, Regulatory Affairs- Medical Device/CMC Position can be located in either the St. Louis, Missouri office or their Clearwater, Florida office relocation is provided Candidate MUST have Medical Device experience and must have written CMC submissions in the past (recent past is preferred) Individual Contributor role Specialty and Diverse Pharmaceutical company is adding to their high profile team competitive base salary, plus bonus, full benefits and other Long....

- Hackensack, NJ

Analytical Chemist Northern New Jersey (Hackensack, NJ - Full Relocation Offered) Competitive Base Salary, 15% target Bonus We have an immediate need for an experienced Analytical Chemist for our New Jersey facility (petro / chemical / industrial manufacturing environment). They have developed some of the petrochemical industry’s most significant process technologies, which are used today to produce millions of tons of petrochemical intermediates in numerous licensed process plants worldwide.....

- Lancaster, SC

Analytical Chemist responsibilities include, but are not limited to, the following :Execute experiments utilizing analytical methods to support preclinical pharmaceutical product development activitiesUse analytical techniques and instrumentation, such HPLC and spectroscopyPrepare test solutions, compounds, and reagentsMaintain laboratory instruments to ensure proper working order and troubleshoot malfunctions when neededBe the owner of technical data you generateRead, write, and prepare....


Job Description: Reports directly to Vice President of Research & Development for investigation of ingredients and product sourcing. Provide scientific assessment of new or existing active ingredients. Investigate formulations and assist formulators with ingredient sources and dosing. Roles and Responsibilities:Assist in the development of new products for the Veterinary Division, including rationale, project timeline, and budget.Assist and support V/P R&D in development of product....

- Lancaster, SC

Roles and Responsibilities:The Quality Control Chemist (QCC) reports to Quality Control (QC) Management.The QCC will stay current on publications released by USP, FDA and other pertinent regulating bodies to ensure the Quality Control Chemistry Laboratory complies in the areas of analytical applications, release specifications, and documentation practices.The QCC will assist in evaluating new testing applications and instrumentation, either developing methods or adopting compendial methods.....


Global Pharmaceutical company (headquarted in West Palm BEach, Florida) is growing and needs a Strong Clinical Lead (someone who mas managed the CRAs and the clinical study trials but can also monitor when needed as Snr CRA). Snr Clinical Research Associate for oncology trials. Must have five to eight years of experience with at least two years of oncology experience. Must come from a Sponsor company (Pharma or Biotech) and be bi-lingual (spanish speaking - many sites are in Latin America).....


Global Pharmaceutical Company out of Madison, NJ and Irvine, CA Position Summary: (Irvine, CA or Madison, NJ) Responsible for leading internal and outsourced Clinical Programming activities in support of Clinical Research studies and managing the design, development, validation, implementation, and oversees ongoing support to electronic case report form (eCRF) systems (e.g. InForm, etc.), external data acquisitions, reporting/business intelligence tools (e.g. SpotFire, J-Review), and other....

- Cranford, NJ

Global Pharmaceutical company is hiring a \ for their growing company. Our Clinical Trainer is responsible for identifying and implementing Clinical Development staff training needs. They may benchmark Clinical SOPs and insure SOP training is completed and up to date. The Clinical Operations Trainer may also periodically co-monitor and evaluate staff performance and provide guidance for performance, improvement and adherence to FDA and SOP requirements. They may liaise with US and Taiwan....


Job Description: We are seeking an experienced and determined professional with a passion for Project Management. As a consultant you will primarily work with clients in the pharmaceutical industry. You will engage directly with key decision makers and have the potential to create true impact. Tasks will mainly relate to Project Management of or within large investment projects. We are looking for a candidate with strong leadership and communication skills who is driven by a desire for....


Global Pharmaceutical company with US Headquarters in Chicago area of Illinois and Boston area of Massachusetts is adding to their team in Deerfield, IL Looking for Project Manager for their Sales/continuing education department PMP preferred 6 month full time contract and then up for renewal $45-50/hour, w-2, health benefits and more Local candidates only OBJECTIVES: - Deliver project objectives within time, resource, and budget constraints - Build and maintain collaborative relationships by....

- Des Moines, IA
new job!

Join a large global leader as, Quantitative Scientist responsible for corporate involvement of data management, digital platform development, prototyping, and problem solving initiatives for matrix organization. In this role, you will use advanced mathematical models, operations research techniques, simulation, quantitative genetics and strong business acumen to deliver insight, recommendations and solutions for Product Development science and business problems. You will formulate and apply....


DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS – CMC Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout lifecycle.....

- Gaithersburg, MD

Director of Lab Operations - CRO Highly regarded contract research organization seeks a Director of Lab Operations to lead P&L business operations for the research group. The Director of Lab operations will:Support implementation of new service linesPlan and direct operational activities leading growth and profitsMaintain exceptional bioanalytical lab operations, focusing on customer satisfaction and successful outcomesEstablish and drive operational management and development....

- Pittsburgh, PA

Director of Regulatory and Clinical Operations The ideal candidate will take on the following tasks: · Contribute to the strategic planning of the company’s regulatory affairs · Lead the implementation of the company’s regulatory strategy and provide evidence-based opinions and advice · Manage all relations with FDA and 510k submission · Provide management with continuous input on regulatory matters and their interactions with business development, clinical development, commercialization,....


Director Analytical Method Development & Validation (GMP BiopharmaceuticalPhD preferred or MS with LOTS (5+ mgt, 10+ GMP)Analytical Method Devt, qualification and validation experience requiredComplex and New Method workLarge Cell experience is a mustWould love to have protein Characterization and analyticsGMP and STRONG leadership (team up to 60-100), Financial Management


My client is in start-up mode seeks a Director to oversee clinical research and drug safety activities along with clinical research strategy. The ideal candidate will take on the following tasks:Oversee clinical study activities.Recruit, manage and develop a small clinical research and drug safety team.Oversee data analysis, evaluation and reporting of clinical data including study reports, FDA and ethics committee progress/final reports, and assist with manuscript preparation.Forecast....


Director, Drug Discovery, Proteomics, Neurodegenerative DiseaseIf you are an accomplished drug discovery leader who would like the freedom of a smaller research institute where your input and opinion really matters and would like to engage in translational research aimed at treating and someday curing a debilitating neurological disease this may be the opportunity for you. My central New Jersey client, a recognized leader in neurodegenerative disease research, seeks a Ph.D. researcher with....


Global Pharmaceutical company with high profile trials is expanding and looking for a Director, Regulatory Affairs for their Global Management Team Competitive base salary and bonus, full relocation and benefits, Long Term Incentives and more Position IDEALLY is located in the Cambridge, MA office (there is small possibility the role can be based in their NJ office) The Rare Disease Global Regulatory Team Lead (GRTL) is part of the Global Regulatory Affairs (GRA) team based in the US. He/she....

- San Francisco Bay Area, CA

Director, Research - Immuno-OncologyOur pre-clinical stage client is working on exciting technology in the field of Immuno-Oncology.This newly created critical leadership has 4 direct reports currently. Ideal candidate will be a Ph.D with strong industry experience in a pre-clinical setting in Immuno-Oncology. This person will outline, implement, and lead the company research strategy and growth towards commercialization. Every day, they will make decisions that matter. Qualifications:Define....

- Palo Alto, CA

The Director is primarily accountable for nonclinical toxicology, working in collaboration with nonclinical pharmacology and pharmacokinetic scientists to drive the overall global nonclinical regulatory submission strategy and coordination for multiple company portfolio products, from research to registration and beyond. The individual has experience in evaluating and responding to inquiries from regulatory authorities addressing global nonclinical development issues in support of IND and....

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