Biotech Jobs in Newark, New Jersey

476 jobs

Job ID: 5805 Position Description: PDI was the first contract sales organization that provides insight-driven multi-channel messaging for established and emerging health care companies. Today, PDI is pioneering new and innovative approaches to how pharmaceutical and medical device companies engage customers. When you join PDI, whether as part of our field sales organization or at our corporate ...

Project Manager III Requirements: -Bachelor’s degree in a scientific/technical or related field from an accredited college or university, and five (5) to seven (7) years pharmaceutical experience. Advanced degree preferred. -Must have worked in a formal project management department or a PMO -Experience in Phases II-IV -CNS/Neurology & Pain experience -MS Project experience is a must -PMP p...

Company is seeking a SeniorDataScientist for Insurance Analytics. Employer paid relocation along with fantastic pay and benefits can be expected! You will apply your highly developed analytical skills to work on all aspects of the insurance value chain, ranging from pricing models, fraud detection, process triaging, and financial risk models to a variety of other analytics solutions. You will al...

MANAGER, GLOBAL DRUG SAFETY REQUIREMENT #15-01016 RECRUITER: CINDI PISNOY JOB LOCATION: JERSEY CITY, NJ JULY 21, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: The Associate Director in the PVRM Safety Information Management group is responsible for analyzing/summarizing complex safety data, and managing the operations of Safety Management Team (SaM...

PROJECT MANAGER, CLINICAL RESEARCH REQUIREMENT #15-01000 RECRUITER: BRIDGET BURNS JOB LOCATION: JERSEY CITY, NJ JULY 17, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Under general direction, plans, coordinates and executes function specific clinical research programs for the clinical evaluation of products. Supervises assigned department staff. E...

R&D PROJECT MANAGER FOR CNS / NEUROLOGY REQUIREMENT #15-00980 RECRUITER: BRIDGET BURNS JOB LOCATION: JERSEY CITY, NJ JULY 13, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: The Manager, R&D Project Management CNS, Internal Medicine, Oncology is responsible for the effective management (organization, planning, execution, monitoring and controlling, a...

MANAGER, CLINICAL RESEARCH REQUIREMENT #15-00972 RECRUITER: BRIDGET BURNS JOB LOCATION: JERSEY CITY, NJ JULY 10, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Under general direction, plans, coordinates and executes function specific clinical research programs for the clinical evaluation of products. Supervises assigned department staff. Essential...

ADVERSE EVENTS / PRODUCT COMPLAINT ASSOCIATE REQUIREMENT #15-01025 RECRUITER: CINDI PISNOY JOB LOCATION: JERSEY CITY, NJ JULY 22, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Under general supervision receives, processes, and evaluates adverse events and product complaints associated with the client’s products in accordance with the current depart...

Position Summary: The Field Test Coordinator will work in the Global Engineering Team reporting directly to an Engineer within the Marketing and Technology group. This group delivers a high quality and innovative service providing solutions to the Technology Group, which has responsibility for the development of new lubricants. A critical part of this development process is to demonstrate the pe...

Job ID: 39434 Position Description: Clean Harbors is the leading provider of environmental, energy and industrial services throughout North America. The Company serves a diverse customer base, including a majority of the Fortune 500 companies, thousands of smaller private entities and numerous federal, state, provincial and local governmental agencies. Through its Safety-Kleen subsidiary, Clean ...

CRA Oncology - Solid Tumor North East Home Based URGENT NEED for experience CRA that is looking for a permanent role working for a full-service CRO. Our client is seeking CRA’s for our specialty business unit which is dedicated to one sponsor. Working in a true partnership environment. This Regionally based CRA supporting sites in the East will be home-based. This role is primarily responsible f...

Everest Clinical Research ("Everest") is a contract research organization providing statistical, data management, statistical programming, medical writing, subject randomization and drug supply management, regulatory submission, and clinical trial management to pharmaceutical, biotechnology, and medical device companies. We serve some of the best-known companies worldwide, and work with many of t...

Must have: - BA/BS - Must possess strong project management skills, preferably in business/health administration or clinical health environment. - Prefer candidate to have project management, document management and coordination experience in pharmaceutical industry. - Proficiency with computer systems (MS Office necessary; Advanced Excel and Word skills preferred) and document management syst...

Seeking a Clinical Manager for a consulting position at a pharmaceutical client. Skills: - ≥ 3 years technical and operational experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organization. - Proven ability to work independently and ability to collaborate and work effectively in teams. - Demonstrated ability to suppor...

Job Number: 430831 Biostatistician III OVERVIEW Be the principal statstical advisor for the Global Medical team. Work with multi-disciplinary team to create strategy and tactics in support of new evidence generation activities e.g. Data mining of Phase 3 data, design of clinical and real world studies etc. Skills: Proficiency with most complex statistical methods and modeling that apply to P...

The entry level chemist with a BS or BA degree in chemistry will be responsible for several areas. This person will be supervised for the first 6 months and then be expected to be self- starting. The first 6 months will be a trial period. Temp to permanent position. We will provide training for the label & SDS software system via webinars conducted by the manufacturer. The typical hours for thi...

Manager, Global Drug Safety Requirements: -BS in Nursing or Pharmacy or PharmD preferred -Knowledge of FDA, EU, and ICH guidelines and regulations -Knowledge of Pharmacovigilance and Risk Management -Knowledge of Coding dictionaries (e.g., WHO ATC drug dictionary, and MedDRA) -Drug safety database knowledge: ARISg, Argus, Business Objects (reporting tool) and Empirica (data mining software t...

Regulatory Affairs Associate Requirements: -BS or MS degree in a scientific field such as Pharmacy, Chemistry, Biology, etc. -2 years in Regulatory Affairs, in generic Pharmaceutical Industry, or 2-4 years’ exposure in Pharmaceutical field such as Analytical, Products Development or Manufacturing Responsibilities: - Preparation of ANDAs, Supplements, Annual Reports and responses to FDA review...

The Senior Research Scientist I is a scientific leader in the AD laboratory, able to independently conduct a broad range of routine analyses, develop and validate methods and document results in notebooks. As assigned, the Senior Research Scientist prepares, reviews and/or approves protocols, reports and investigations. The Senior Research Scientist mentors other analysts in the execution of labor...

This position is responsible for independently planning and execution of formulation development strategies. The person functions as a subject matter expert in dealing with government agencies and external contract research organizations. Coordinates with other departments to get the advancement of key R&D goals. Essential Functions and Responsibilities: Designs and conducts pre-formulation, for...