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Job Title: Specialty Pharmacy Director Location: Baltimore, MD PRINCIPAL ACCOUNTABILITIES: The position reports directly to the Senior Director of the Pharmacy Evaluation & Oversight and is a critical leadership position within the unit responsible for understanding the specialty marketplace, opportunities for utilization management, and cost containment. The Director of Specialty Pharmacy will interact frequently with the EVP of Medical Affairs, the CEO, and other senior leaders across....


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


Senior Principal Mechanical Engineer - R&D Fremont, CA Summary of the Senior Principal Mechanical Engineer - R&D: Sr. level Principal Mechanical Engineer with strong medical device design and development experience is required to act as a Technical leader and provide work direction to engineers across multiple programs for one of our clients in California. This is a long-term Fortune 500 client of ours who has engaged us to locate team members to be part of their advanced development....


Well-established Medical Device manufacturer has a unique opportunity for a Technical Service Manager for their line of Dialysis equipment. This individual may be located near a major airport on the east coast.The Technical Service Manager will develop and manage end-to-end service of dialysis equipment in North America. This includes the installation, service and repair, and assisting with in-servicing the Sales and Clinical teams, and with external customers, on the (non-clinical) use of....


Position Overview The Sr. Manager will represent Regulatory Affairs for pharmaceutical development projects and marketed products. Working with manager, responsible for development and communication of global regulatory strategy on R&D project teams. Main Areas of Responsibilities The Sr. Manager Regulatory Affairs will ensure technical accuracy and regulatory compliance of all submissions for which they are responsible and ensures that applications are executed appropriately and submitted


Job Category: Research & Development The Senior Clinical Program Leader I3 (Inflammation, Immunology and/or Infectious Disease) is accountable for the operational strategy, planning and execution of the clinical development portfolio up to LIP for the designated Discovery and Translational Area (DTA).You provide the primary interface between the I3 DTA and pRED’s the Clinical Program Execution (CPEX) function in Clinical Operations, oversight for program and study management, line....

- Cincinnati, OH

Lead and participate in continuous improvement projects supporting the manufacture of sterile pharmaceutical products for commercial and clinical supplies. Define, measure, analyze, and propose improvements to current processes and systems. Author and execute engineering studies, technical reports, change controls, and validation protocols necessary to support implementation of project. This position will work closely with Line Management and Department Leaders to execute projects focused on....


Are you a RN who meets the qualifications of an Emergency Room Director? This is a VERY High volume role. We need someone with experience at a large facility if you have not been a director. : 5 years progressively responsible clinical experience working in the ER5 years progressively responsible high level management experience in a VERY high volume ER. Client prefers someone who is already in a Director role.Does your management expereince includes management of the ER, revenue....


Reporting to the Vice President, Drug Development-Generics, the Director, Project Management will use the global PDP (Product Development Process), allied systems & tools, to plan and manage/coordinate resources and activities related to product development and maintenance of business projects throughout Global R&D, and other company organizations. Responsibilities: Responsibilities:Champion and lead projects for new generic product development.Management of project team members from....


My CLIENT, is a New Jersey based, stable, not-for-profit biomedical research organization devoted to developing drugs that will slow the progression of neurodegenerative disease (NDD) and provide meaningful clinical benefit to patients. They are seeking a junior, but highly motivated and organized individual to assist their Science Directors managing projects in the clinical portfolio (including, but not limited to clinical studies and trials). They want a Bachelors or Master’s degree in life....


POSITION OBJECTIVE: Responsible for leading the CMC (Chemistry, Manufacturing and Controls) regulatory function, the Senior Manager, Regulatory CMC will collaborate cross-functionally to develop the CMC regulatory strategy, provide guidance to broader CMC functions, and drive CMC regulatory filing(s). Working collaboratively with senior leadership to develop CMC regulatory strategies for one or more investigational and/or commercial products this position will lead the preparation and filing....


Overview: The Surgical Regulatory Affairs Sr Manager handles all regulatory development aspects of surgical devices. The incumbent participates on the product development team to provide regulatory guidance for surgical devices assigned. They also manage relevant regulatory strategy components and interactions with Regulatory Authorities for their assigned surgical products and may perform due diligence efforts on new product opportunities. Responsibilities: Responsibilities may include but....

- Any US State

Pharmaceutical company hiring MSLs- GI and Pain and Addiction There is three openings for an MSL in Pain and Addiction to cover the whole United States in the: East, Central and West. There is one openings for an MSL in GI for Texas region only please only apply if you have previous and recent Medical Science Liaison experience for the pharmaceutical or biotech or medical device industries looking for three or more years of experience as an MSL The Medical Science Liaison (MSL) plays a crucial

- Waltham, MA

TOP TIER PHARMACEUTICAL COMPANY in MASSACHUSETTSglobal biopharmaceutical company developing innovative medicines The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates Position SummaryWe have the need for a highly collaborative, experienced Manager of Medical Writing Operations to join our team based in MA. The position reports into our Director of Medical Writing and will lead writing responsibility of documents which ensure....


The Senior Manager Clinical Operations is responsible for developing operational strategy for one or more clinical studies, and leading the cross functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Senior Manager Clinical Operations Lead will independently plan all aspects of the clinical operations for one or more clinical studies and oversee the execution of


Pharmaceutical client in NYC hiring two Clinical Research Study Managers for their Global Trials The Clinical Research Study Leader (CRSL) will provide leadership to global Study Management Teams responsible for delivering First in Man, Proof of Concept through to Phase 3 registration studies in various indications. The CRSL will manage a number of studies, either for a single indication or across different indications. The CRSL is accountable for the strategic and tactical study activities,....


Director of Clinical Development Cardio This global Pharmaceutical company is the worldwide biologics research and development leader. Here, you’ll have the opportunity to make a difference in people’s lives every day. As one of the world’s premier biotechnology companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease. As a Director, Clinical Development in Gaithersburg MD or Cambridge UK, you’ll play a pivotal role in....


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....


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....


Global Pharmaceutical Leader is looking for consultant (all levels) Clinical Managers for their growing Clinical Development team Accountable for leading the operational study team, which is responsible for the execution and delivery of quality studies, including in-process quality control activities (e.g. quality checks and balances to ensure inspection readiness, enrollment, metrics, milestones, timelines and budget). This position requires advanced knowledge of the functional disciplines....

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