Biotechnology & Pharmaceuticals industry jobs in Newark, Delaware

Johnson & Johnson companies are equal opportunity employers. Medical Surveillance Systems Manager-9957130604 Description Animas Corporation, a member of the Johnson & Johnson Family of Companies, is recruiting for a Medical Surveillance Systems Manager for its location in West Chester, PA. Animas Corporation develops and manufactures glucose management systems that help people living with diabetes...
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Johnson & Johnson companies are equal opportunity employers. Worldwide Director, Human Resources - Neuro-3157130306 Description DePuy Orthopaedics Inc. is recruiting for a Worldwide Director, Human Resources - Neuro position located in either West Chester, PA or Raynham, MA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic and neurological ...
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Principal Objective(s): The Principal Medical Writer researches, writes, and edits complex clinical documents for submission to regulatory agencies to meet the objectives of Clinical Research and Development (CRAD). Major Duties and Responsibilities: Preparation of clinical study reports, integrated summaries of safety and efficacy, and other high level clinical summary and overview documents for ...
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The Data Standards Technical Specialist follows established standards and procedures to provide a wide range of data programming duties associated with the delivery of data and documentation that complies with CDISC standards, related FDA guidance and internal standards. Major Duties and Responsibilities: · Follows established procedures for developing, implementing and maintaining processes to as...
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The Intake Coordinator will be responsible for the Intake of a Service Request Form (SRF) up until Shipment. This role’s primary responsibilities will consist of a full benefits investigation (to establish coverage for services under the Major Medical and/or Pharmacy portion of a patients plan) of which should be completed within 24 hours of the receipt of a completed SRF, initiate prior authoriza...
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The Senior Clinical Programming Specialist follows established standards and procedures to provide a wide range of clinical programming duties involving designing, developing, evaluating and modifying computer programs to analyze and evaluate clinical data. The position will develop activities within the scope of a project. Major Duties and Responsibilities: Follows established procedures for deve...
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Principal Objective(s): The Senior Director, Clinical Development Operations is a key role for the strategic planning and implementation of clinical projects conducted by ViroPharma. The Senior Director, Clinical Development Operations will provide effective leadership, oversight and mentoring of the global clinical operations department thereby maximizing the potential of the global clinical oper...
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Principal Objective(s): The Senior Director, Global Clinical Pharmacology will provide scientific, technical and strategic leadership and expertise to the Clinical Pharmacology Department. This individual will have responsibility for the design and execution of all Clinical Pharmacology research and development activities. The individual will bridge activities and relationships stemming from bench...
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Principal Objective(s): The Clinical Data Associate at ViroPharma Incorporated follows established standards and procedures to provide a wide range of clinical data management duties to ensure the accuracy and completeness of clinical trial data. Major Duties and Responsibilities: Follows established GCP procedures and practices for implementing and maintaining processes to assure departmental goa...
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Principal Objective(s): Work within ViroPharma to oversee the management of Phase I through IV clinical research studies conducted in Emerging Market countries to ensure compliance with regulatory requirements (e.g. GCP/ICH), overall quality study conduct and adherence to study timelines. Major Duties and Responsibilities: Identification, selection and oversight of Phase I-IV Clinical Research sit...
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Principal Objective(s): As an integral part of the Patient Services Center (“PSC”) department, the Patient Care Coordinator shall be accountable to relationship management of its customers. This includes regular calls to patients related to insurance, shipment of drug and available marketing programs; working closely with patients that are enrolled in the ViroPharma Charitable Foundation (“VCF”) t...
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- Ensure group benefits programs (including but not limited to) medical, dental, vision, group life, disability, Workers' Compensation, unemployment, education assistance, voluntary benefits, 401(k), FSA, COBRA, HIPAA, FMLA and OSHA, are being administered in accordance with all compliance and government provisions - Ensure timely and accurate transfer of information, Payroll and other authorized ...
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Our client, a Pharmaceutical Company in King of Prussia, is looking for a FirstDoc developer/engineer/analyst for a contract opportunity through the end of 2013. Required Skills and Experience: 2 to 5 years experience configuring, supporting and/or customizing the FirstDoc R&D application. Ability to analyze business requirements and author technical documentation including IQs and Tech Specs. Exp...
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Our client, a Pharmaceutical Company in King of Prussia, is looking for a R&D IT Application Support Engineer for a 1 year contract opportunity. Required Skills and Experience: A software engineer with 2+ years experience supporting, configuring and/or customizing R&D applications within a Pharmaceutical company. Experience with the FirstDoc, ISI Publisher, ClinSupplies or Insigh for Publishing ap...
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Description Janssen Research & Development, LLC., a Johnson and Johnson Company is hiring a Senior Scientist, Drug Product Development - Biologics to be located in Radnor, PA. Janssen Research and Development , LLC develops treatments that improve the health and lifestyle of people worldwide. Research and development areas encompass novel targets in neurologic disorders, gastroenterology, oncology...
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Our requirements include: · High school diploma or equivalent, as well as Phlebotomy certification (where required) from an accredited agency · Completion of an approved phlebotomy training course (or equivalent) · Valid driver's license with clean driving record · Minimum of 2 years of experience as a patient service technician/phlebotomist · Proficiency in the following: blood collection by veni...
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Clinical Data Manager Quality Data Services, Inc., a highly respected Clinical Research Organization in King of Prussia, PA, is seeking a Clinical Data Manager to manage the timely and quality completion of databases of clinical studies contracted to Quality Data Services, Inc (QDS), manage internal data management and database development staff, and act as liaison with sponsor and/or third-party ...
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Asset Management System (RAM) Consultants We have an immediate requirement for a team of 4 to 6 consultants to handle RAM (Blue Mountain) system activities at 2 sites of a reputed pharmaceutical company. Consultants are required to be on-site every day, and should be willing to start within 2 weeks of notice. We welcome resumes from qualified consultants with extensive experience and background in...
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1812PMW Senior Director, Clinical Development Operations Location: Philadelphia Area Salary: Up to $200K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking a Senior Director, Clinical Development Operations that will provide effective leadership, oversight and mentoring of the global clinical operations department thereby maximizing...
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1813PMW Assistant Director of Regulatory Affairs, CMC Location: Philadelphia Area Salary: Up to $130K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking an Assistant Director, Global Regulatory CMC that will be responsible for managing and maintaining multiple US and international (including emerging market) registration dossiers wh...
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1814PMW Assistant Director, Clinical Development Operations, Emerging Markets Location: Philadelphia Area Salary: Up to $130K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking an Assistant Director, Clinical Development Operations, Emerging Markets to oversee the management of Phase I through IV clinical research studies conducted ...
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1811PMW Director of Regulatory Affairs Location: Philadelphia Area Salary: Up to $160K + Bonus CLICK HERE TO VIEW VIDEO! We are a growing, dynamic, customer focused pharmaceutical company that is seeking a Director, Regulatory Affairs to provide oversight, direction and leadership for all regulaotry activities related to assigned therapeutic areas. WHAT WILL YOU DO HERE? - Develop regulatory strat...
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Pharmaceutical sales opportunity for motivated, driven, results oriented individual. You are encouraged to apply if you are a self-starter and possess an entrepreneurial spirit looking to further your career development with a rapidly growing specialty pharmaceutical company. Responsibilities - Utilize sales data to create and execute a territory management plan - Expand and develop sales territor...
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Description Janssen Scientific Affairs, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Medical Science Liaison - CNS position to cover the following region: PA, MD, OH, DE & DC. Janssen Scientific Affairs, LLC is dedicated to providing medical information and consultative support to a number of J&J pharmaceutical companies. The company's mission is to create t...
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Director ICT - Bioinformatics / Genomics / Big Data- based near Cambridge, UK The Wellcome Trust Sanger Institute is a charitably funded non-profit organisation and world leader in genomic research, with an expanding scientific programme dedicated to understanding gene function in health and disease. The Director of Information & Communication Technology (ICT) represents a significant and exciting...
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