- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... Data Ops for EDC, edit checks, data quality listings, SAP , Data Mgmt plan; Reviews patient population and protocol...Planning and Execution: Provides input on major milestones of trial , clinical trial plan and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …training and ensure effective implementation of SDTM, ADaM and TLFs standard in clinical trial data analysis- Develop and maintain necessary programming macros ... review, review analysis dataset specifications and ensure correct interpretation of SAP , develop independent programs to validate stud level analysis dataset and… more
- Actalent (Thousand Oaks, CA)
- …Manage end to end process for clinical site contracts and clinical trial related consulting agreements (including contracts, amendments and termination ... Disclosure Agreements as appropriate * Manage contracting process with Clinical Trial Related Consulting Agreements * Manage...OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience - Recent… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... Data Ops for EDC, edit checks, data quality listings, SAP , Data Mgmt plan; Reviews patient population and protocol...Planning and Execution: Provides input on major milestones of trial , clinical trial plan and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... Data Ops for EDC, edit checks, data quality listings, SAP , Data Mgmt plan; Reviews patient population and protocol...Planning and Execution: Provides input on major milestones of trial , clinical trial plan and… more
- Actalent (Thousand Oaks, CA)
- …study start up and conduct activities Responsibilities Manage end to end process for clinical site contracts and clinical trial related consulting agreements ... track Confidential Disclosure Agreements as appropriate Manage contracting process with Clinical Trial Related Consulting Agreements Manage all study-related… more
- Sanofi Group (Cambridge, MA)
- …at the investigator meetings + Ensure continuous medical review of aggregated data during clinical trial conduct (DRSR, safety, stat outputs of blinded data, ) ... ** Clinical Research Director - allergy-immunology-dermatology** The Clinical...com, adjudication ) with operational support + Co-Develop the SAP in collaboration with bio stats + Responsible for… more
- Merck (West Point, PA)
- …and associated regulatory submissions for Investigational New Drug applications and Clinical Trial Applications in relation to complex/niche supply chains ... procedures, and to provide independent assurance that delivers high quality data and clinical supplies. This position reports to the Associate Director, Global … more
- System One (Basking Ridge, NJ)
- …Salary: $180k - $195K Must Haves: Oncology lead experience. PhD 5+ years Oncology clinical trial experience OR Master in Biostatistics - 8+ years experience. ... Job Title: Associate Director, Biostatistics Client - Global Pharmaceutical Company...Development, Case Report Form (CRF; review), Statistical Analysis Plan ( SAP ), Statistical Analysis, Results Interpretation, and clinical … more
- Ascendis Pharma (Palo Alto, CA)
- …and sample size calculation, case report form (CRF) design, statistical analysis plan ( SAP ), through clinical study report (CSR). Author documents or sections of ... the business, from drug development to marketing. Position Summary The Associate Director of Biostatistics will provide statistical leadership, oversight, expertise… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …training and ensure effective implementation of SDTM, ADaM and TLFs standard in clinical trial data analysis - Develop and maintain necessary programming macros ... review, review analysis dataset specifications and ensure correct interpretation of SAP , develop independent programs to validate stud level analysis dataset and… more
- ThermoFisher Scientific (New Brunswick, NJ)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... **Job Description** **Title: Labs FSP - Associate Research Scientist - Project Management** **Location: New Brunswick, NJ** This is a Monday** **-Friday position on… more
