R & D Jobs in Florham Park, New Jersey

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151 Florham Park, NJ R & D jobs found on Monster.

Jobs 1 to 20 of 151
Support study data management and data cleaning process on an ongoing basis, applying study specific documents and conventions. Identify and issue queries, incorporate query replies, track query status and apply permissible clarifications using the EDC (e.g., RAVE) and related systems (e.g., SAS, jReview, etc.). Assist in documentation gathering and archiving. Minimum 3 years as a Study Data Mang...
Currently we have a temporary opening for a Facilities Engineer to support a company located in the Short Hills, NJ area.   Responsibilities: Manage major construction projects at multiple North American sites. Developing design concepts with the users and design engineering firm Developing request for proposals to bid projects, coordination with customers, contractors and consultants, Revie...
Job ID: 4299 Position Description: Interpace Diagnostics, LLC focuses on assisting molecular diagnostics companies to commercialize their products and offers a full suite of services that includes field sales management, reimbursement support, marketing, and comprehensive financial partnerships that can meet almost any need. A full-time Diagnostic Account Executive is needed to exemplify the va...
Job ID: 4294 Position Description: Company Overview At EngageCE, a division of PDI, Inc., we believe instilling positive behavior within the practice is the cornerstone of providing optimal patient care. Many practices face challenges and old habits that impact their ability to follow care recommendations, which can negatively impact patient outcomes due to: • Difficulty establishing and maint...
Outstanding CDM opportunity available with a growing clinical research organization in the Northern New Jersey area. A positive work environment and recognition of the importance of work life balance has led to employee satisfaction and company success. A competitive salary and comprehensive benefits package are offered. Job responsibilities: The Sr. / Clinical Data Manager leads data management...
PRINCIPLE ACCOUNTABILITIES · To support clinical trials at assigned sites including the responsibility of site management by coordinating all activities pertaining to qualification and initiation of and ongoing site support for the clinical trial. · To provide in-service education and training for physicians, hospital personnel and office staff on study related documents and devices in support o...
Regulatory CMC Associate.....URGENT NEED!! Duties: Under supervision, provide strategic and operational global CMC regulatory direction and documentation for MARKETED PRODUCT maintenance. Experience desirable. The following activities may be performed within this capacity: Provide and/or implement global CMC regulatory strategy for products. Lead or contribute to global CMC submission activiti...
Company: Yoh Clinical Research Associate needed for a contract opportunity with Yoh's client located in East Hanover, NJ. What You'll Be Doing: - Responsible for implementation of operational aspects of clinical development and medical affairs trials in the US Hematology franchise. - Interfacing with the oncology therapeutic area global and U.S. clinical team members to conduct trials in maint...
Pharma client seeks a Pharmaceutical Quality Systems Project Manager for a 6 month contract with possibility of extension. ***Travel to local sites required*** Quality Systems Duties: - Perform project management functions for transfer of Quality Systems for site to site transfer: FARs, Deviations, CAPA, Change control, Documentation, Training systems, Complaints, Release, etc. - Lead activitie...
GPV Alliance Management Contractor Requirements: -Bachelor’s degree in the legal field, at least 2 years of relevant work experience contract drafting and negotiations and experience working with contract databases. -The ideal candidate will also have experience working in the pharmaceutical industry environment and will have knowledge of global pharmacovigilance regulations and concepts. -Exc...
Requirements: -MD with 5+ years of pharmaceutical experience; specializing in cardiovascular, pulmonary or critical care medicine. -Expertise in Nephrology. Responsibilities: -Individual will support US medical affairs focusing on phase 4 development program and support of technical information regarding cardiopulmonary products. Location: Whippany NJ Duration: 10-20 hours per week for perio...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Qualifications: Minimum of a BS degree Regulatory experience preferred Pharmaceutical/Biological manufacturing or Quality experience preferred Experience preparing CMC (Chemistry, Manufacturing, Controls) post approval submissions preferred Experience with Trackwise and regulatory tracking databases preferred Proactive and highly productive Sound judgment Attention to detail Strong writte...
LEO Pharma is an independent, research-based specialty pharmaceutical company committed to the discovery and development of novel drugs for patients within the area of dermatology in the U.S. For 105 years our products, which are marketed in more than 100 countries worldwide, have improved the quality of millions of people's lives around the world. We understand that people power our success. Our...
The RBA Group is a multi-disciplined Engineering, Architectural and Planning Firm. We offer a competitive salary as well as a wide cadre of benefits which include: 4-day work week 4 weeks of paid time off PPO Medical Plan with 4-tier coverage structure Dental Plan Vision Plan 401k Savings Plan which includes a company match Company paid Life and AD&D Insurance Flexible Health and Dependent...
LEO Pharma is an independent, research-based specialty pharmaceutical company committed to the discovery and development of novel drugs for patients within the area of dermatology in the U.S. For 105 years our products, which are marketed in more than 100 countries worldwide, have improved the quality of millions of people's lives around the world. We understand that people power our success. Our...
LEO Pharma is an independent, research-based specialty pharmaceutical company committed to the discovery and development of novel drugs for patients within the area of dermatology in the U.S. For 105 years our products, which are marketed in more than 100 countries worldwide, have improved the quality of millions of people's lives around the world. We understand that people power our success. Our...
Qualified candidates will have 5 years of Medical Information experience: Writes and updates relevant, unbiased custom and standard response documents and product profiles for products to ensure information provided to customers represents the most complete and accurate information. Acts as expert in therapeutic areas of responsibility and uses this expertise to influence appropriate decision ma...
Outstanding opportunity for a leading pharmaceutical and OTC organization. This is a full time position offering a competitive salary and benefits. The position will be based in the White Plains, NY area. Relocation assistance provided. Job Information: · Develop and review of clinical protocols; review of scientific literature; and work with physicians and external consultants to develop clinic...
Exciting opportunity to join a select team that is leading the way in the Pharmaceutical/Biotech industry.Competitive salary, bonus incentive program and comprehensive benefits package offered. The position will serve as a subject matter resource for identified area(s), including relevant activities in assigned Therapeutic Area program(s) or Business Objects program. Job Responsibilities: · Wor...

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