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Support HEOR (Health Economics and Outcomes Research) activities for Sanofi Genzyme commercial and pipeline products. Support the current HEVA (Health Economics and Value Assessment) team as required. Work cross-functionally with..
We are looking for a Regulatory Affairs Specialist for a contract opportunity for a huge pharmaceutical company. Type: consulting/contract Duration: 6 months Location: Swiftwater PA Job Description: The Regulatory Affairs..
The Manager of Print Production is responsible for managing the print process and ensure timelines are captured and met from development through the review process, production and dissemination. Exceptional communication..
Looking for a career change or first employment? Job Title: Customer Care Rep (Spanish Speaking) Location: Flushing, Queens NY Company: Kryshundayal Agency LEADS ARE AVAILABLE Description: We provide .....
Onsite San Francisco M-F Ideal Candidate-High functioning clinical trial associate (CTA)/Junior level clinical trial manager who is able to perform daily clinical trials activities, as well take on stretch responsibilities..
Assist in the packaging of pharmaceutical products. Position required adherence to Safety Rules, Good Manufacturing Practices and Standard Operating Procedures. Experience: 3 to 6 years. Individuals supporting this position will..
Ideal Candidate-High functioning clinical trial associate (CTA)/Junior level clinical trial manager who is able to perform daily clinical trials activities, as well take on stretch responsibilities such as writing and..
Aequor Technologies, Inc. is a global consulting and staffing services company providing value services to the Pharmaceuticals, Life Sciences, and Healthcare industries for nearly 20 years. We have strong relationships..
This position can sit on-site in Thousand Oaks, CA or can be REMOTE. Day to Day Responsibilities: Lead the development of ADaM Standards. Provide strategic direction in the adoption and..
Job Title: Technical Writer II CMC Regulatory Writing Duration: 21 Months Location: Bridgewater, NJ Job#: 8183633 The candidate must have excellent Chemistry, Manufacturing and Controls (CMC) technical writing and communication..
The Clinical Trial Operations Manager (CTOM) is responsible for all aspects of clinical trial including key data management activities in compliance with GCP?s, SOPs and standards within established timelines and..
Actual Job Title = SAS Programmer Duration = thru end of the year, possible extension Location: Berkeley Heights, NJ Job#: JP00006555 Typical Daily Work Hours = 8am to 5pm (some..
***Please note, this position is not on the current rate card. Use Title Pharmacovigilance Scientist II. Bill Rate commensurate with experience not to exceed rate range (USD)(USD)102.84 - (USD)134.90/hr. The..
Actual Job Title = SENIOR Data Manager Duration = One year from start date Typical Daily Work Hours = 8am to 5pm (some flexibility in start/end times) Weekend & OT..
The Clinical Trial Operations Manager (CTOM) is responsible for part of the operational aspects of clinical trial oversight including the delivery of every study on time within budget and scope..
Using references and knowledge of relevant guidance/regulatory documents, contractor will perform compliance activities supporting Change Control and Regulatory documentation related to: registration support artwork management specification updates other quality activities..
Actual Job Title = Statistician in Clinical Trials DURATION = one year from start date Location: Berkeley Heights, NJ Job#: JP00006535 Typical Daily Work Hours = 8am to 5pm (some..
CUSTOMER SERVICE CONSULTANTS NO EXPERIENCE NECESSARY / TRAINING AVAILABLE We are the nations largest union labeled supplemental benefits company, and are currently experiencing explosive growth! We .....
This position is not to directly manage trials but does require several years of Clinical Trial Experience in any therapeutic area (Pharma or Biotech) Please try to stay to the..