Full-Time Customer Service Representative jobs in the Biotech, R&D, Science category

Do you want to work in the fastest growing industry? Do you possess excellent interpersonal skills with the ability to multitask and service customers in an effective manner? [1]POSITION SUMMARY: [2]Monster has partnered with a leading pharmaceutical services company with a location in the Naperville, IL area on their search for Customer Service representatives for a new facility opening soon. The...
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Senior Biostatistician (Senior Manager) Role Description To lead and perform statistical activities on the assigned project/protocols, including input to clinical design, prepare statistical section of protocol, Statistical Analysis Plan, Statistical Analysis Report, Statistical programming for key statistical techniques to be used in trial analysis and other statistical activities associated with...
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Responsibilities Candidate, as a member of Biostatistics and Programming Department, will provide statistical supports for Phase 2/3 clinical studies and/or perform statistical methodology research. The candidate will closely collaborate with project teams consisting of clinicians, project managers, clinical trial managers, data management and other functions. Activities include preparing study pr...
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TechData is hiring SAS/Stat Programmers (Some can be telecommuting), Biostatistician (Can telecommute), and Architect in Gaithersburg, MD. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitive pay rate and benefits. TechData is the leading supplier in the pharmaceutical consulting industry. Sr. SAS Pr...
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Excellent opportunity for experienced Biostatistician! Fast-growing and very stable pharmaceutical company! Excellent work environment! Long-term contract! The client is looking for a self-motivated, PhD or MS statistician with experience in clinical trials who will: • Provide statistical support to protocol; review and provide comment on the study protocol. • Review and approve CCG plan, data cle...
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Lexicon is a biopharmaceutical company focused on discovering and developing breakthrough treatments for human disease located in The Woodlands, Texas. We currently have multiple programs in clinical development for diabetes, irritable bowel syndrome, carcinoid syndrome and other indications, all of which were discovered by our world class research team. We have used our proprietary gene knockout ...
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Sr. Study Manager The Study Manager is responsible for • Leading one or several cross functional study teams (and/or sub-teams) to deliver clinical research studies on time, within budget and with good quality in compliance with Regulatory Authorities regulations/guidelines and Celgene SOPs/WPs. • Sharing best practices • Contributing to process improvement initiatives Study Manager Responsibiliti...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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Senior Associate, SAS Programming This individual will be responsible for SAS programming Role Senior Statistical Analyst Role Description To lead and perform statistical activities on the assigned project/protocols, including input to clinical design, prepare statistical section of protocol, Statistical Analysis Plan, Statistical Analysis Report, Statistical programming for key statistical techni...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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TechData is hiring Biostatistician (some can telecommute), SAS Programmer (Some can be telecommute), Sr. Clinical data manager, Sr. Medical Writer,Life Sciences Hub (LSH) Consultant and Oracle Clinical for Global Librarian/Modeler, Biomarker Trial head for our pharmaceutical clients in Northern NJ. Please see below requirements and send your inquiry and resume to: dan.chen@techdataservice.com or r...
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Job Summary: The purpose of this job is to create, without supervision, any type of clinical regulatory document (e.g., protocol, CSR, CIB, clinical sections of IMPD and CTD) according to company guidelines and international governmental regulations and to present clinical data objectively in a clear, concise format. This position is for an independent, proactive, experienced medical writer with d...
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Excellent opportunity for experienced Biostatistician! Very stable, fast-growing pharmaceutical company! Excellent work environment! Long-term contract opportunity! Description of Services Required: • Support clinical trial design and protocol concept sheet development • Develop protocols especially for statistical section • Participate study related activities and provide statistical support such...
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Excellent opportunity to work with a fast-growing pharmaceutical company! Great work environment! Long-term contract opportunity! Description of Services Required: · Support clinical trial design and protocol concept sheet development · Develop protocols especially for statistical section · Participate study related activities and provide statistical support such as safety review, interim analyses...
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TechData is hiring SAS Programmer (Some positions can be telecommute), clinical Data Analyst, Biostatistician (some can be telecommuting), Clinical Data Manager, Clinical Outsourcing Consultant, Clinical Research Scientist for our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData is...
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Medical Monitor Job Description: The Medical Monitor is accountable for patient safety and provides medical guidance during study design and execution. In addition to study level activities, the MM will participate on Program Teams, participate in standing committees, review compounds for potential in-licensing including performance of due diligence reviews and provide assistance to New Business D...
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TechData is looking for Validation Analyst (6 positions), Sr. Drug Safety Associate, Computer System Quality Assurance, SAS Programmer (Some can be telecommuting), Biostatistician, Sr. Clinical Data Manager for our pharmaceutical clients in SFC, CA. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitiv...
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PRINCIPAL REGULATORY WRITER Locations: Boston, MA; Philadelphia, PA; Nashville, TN Our client is coming off a year of substantial growth, and this has created an opportunity for a highly experienced Principal-level Regulatory Writer. They also have a highly stable environment, having never downsized a performing writer in over 20 years. The Principal Regulatory Writer is involved in driving the cr...
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PRINCIPAL REGULATORY WRITER Locations: Boston, MA; Philadelphia, PA; Nashville, TN Our client is coming off a year of substantial growth, and this has created an opportunity for a highly experienced Principal-level Regulatory Writer. They also have a highly stable environment, having never downsized a performing writer in over 20 years. The Principal Regulatory Writer is involved in driving the cr...
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PRINCIPAL REGULATORY WRITER Locations: Boston, MA; Philadelphia, PA; Nashville, TN Our client is coming off a year of substantial growth, and this has created an opportunity for a highly experienced Principal-level Regulatory Writer. They also have a highly stable environment, having never downsized a performing writer in over 20 years. The Principal Regulatory Writer is involved in driving the cr...
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