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

TechData is hiring SAS Programmer (Some positions can be telecommute), Biostatistician (Some position can be telecommuting), Database Developer, Sr. Clinical Data Manager, Medical Writer, Clinical Manager, Paralegal, Outsourcing managers for our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.c...
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Sr. Statistician Come experience the growth. Frontage is a global, integrated contract research organization (CRO) serving clients within pharma and biotech companies. With headquarters in Exton, Pennsylvania, near Philadelphia, and a division in Shanghai, China, we offer drug R&D services that combine unmatched quality, speed, and value. This role is based in our Exton, PA, Headquarters. Responsi...
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Expert Clinical Manager 6 month, renewable contract w2 candidates only Duties: Clinical trial management of studies under the management of the Clinical Trial Head (CTH)/Lead CTH including all study-related activities and CRO/ vendor management and oversight. Other duties include organizing/compiling/leading the preparation of various regulatory documents including CSR appendices, Investigator Bro...
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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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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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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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Basic Qualifications Masters degree in Statistics/Biostatistics or other subject with high statistical content, and 3 years of post-graduate statistical experience in the pharmaceutical industry or medical research Or, Doctoral degree in Statistics/Biostatistics or other subject with high statistical content Communication of statistical information (written and oral) Demonstrated effective communi...
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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 hiring for SAS/Statistical Programmer(Some positions can be telecommuting), Biostatistician(Some can be telecommuting), Sr. Clinical Data Manager, Clinical database Programmer/Analyst, Manager of Peoplesoft HR Application, Clinical Study Manager, Clinical Outsourcing Consultantfor our pharmaceutical clients in Northern NJ. We also have similar positions in MA, PA, MD, DE, NC and CA. Pl...
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We are currently seeking an experienced Medical Writer who will mainly be responsible for writing, editing and reviewing Clinical Study Reports. This role requires at least five years of experience in medical writing including writing Clinical Study Reports (CSR’s) for a pharmaceutical or biotech company. The ability to analyze and synthesize data independently as well as manage multiple projects ...
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We have several positions and are eagerly reviewing new candidates. Please submit your resume if you feel you meet the necessary requirements below: The Clinical Trials Associate (CTA) is involved in the conduct of the study and interfaces with the Study Manager and the Study Team. Requirements: BA/BS in directly-relevant discipline or equivalent experience required At least 2 years experience as ...
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TechData is looking for Validation Analyst (6 positions), Sr. Drug Safety Associate, SAS Programmer (Some can be telecommuting), Biostatistician (Telecommuting), 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 competitive pay rate and bene...
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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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Member of the clinical team will be responsible for late stage drug development according to Federal Regulations and ICH guidelines. This would include writing study protocols, planning study conduct, interacting with study team members, training of study investigators, planning and running study meetings and providing clinical feedback on Clinical Study reports. Responsible for the initial budget...
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The Clinical Project Manager is responsible for the overall management of multiple studies of various complexity and broader geographic scope. The Clinical Project Manager ensures that activities which impact a study(s) are performed according to the development plan for the study(s). The Clinical Project Manager is responsible for the direct management of junior study personnel. Responsibilities:...
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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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