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Qualifications and Experience: A Master’s or Ph. D. Degree in statistics, biostatistics, epidemiology, public health, bioinformatics, mathematics, and computer sciences, with SAS certified Base, Advanced, and Clinical Trials Programmers are highly preferred; with exposure/experience in clinical trial statistical programming and/or data analysis is desirable.
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The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines.
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Experience handling large data sets, familiarity with data quality issues and with programming in a clinical research environment. The Programmer Analyst II will provide statistical support for new and ongoing HIV and other emerging infectious disease studies conducted by MHRP, EIDB, and affiliated programs, involving clinical observational research, laboratory research, clinical trials, and other research studies.
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The Clinical Research Coordinator will work with faculty, fellows and residents to organize and participate in all operational aspects of ongoing clinical and health services research in Pediatric Emergency Medicine.
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Clinical Research Coordinator - Pediatric Emergency Care Applied Research Network. The Clinical Research Coordinator will provide research support for the Pediatric Emergency Care Applied Research Network (PECARN) clinical research program.
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Sansum Diabetes Research Institute has an opportunity for a full-time, board certified, or board-eligible Endocrinologist to serve as a Clinical Research Investigator. SDRI is a non-profit organization and center of excellence with a mission to improve the lives of people impacted by diabetes through research, education, and clinical care.
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Develop/implement new and creative data capture approaches to streamline our clinical research databases. 10 years in leadership positions in clinical research (Manager level or above.
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Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine.
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In this fully remote position, you will have the chance to showcase your expertise in statistical programming while contributing to cutting-edge biotech research and development. To excel in the role of A Senior Principal Statistical Programmer at Beacon Therapeutics (USA) Inc., proficiency in SAS programming language for clinical studies is essential.
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Experience with SQL programming and data preprocessing for research studies are also required. Previous experience with high-level programming languages such as SAS, R Statistical Programming Language, SPSS, C/C.
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The Associate Director, Global Health Economics & Outcomes Research (GHEOR) Analytics, develops and implements HEOR Analytics strategy, including real-world study design and conduct, identification of data sources, and execution of publication plan.
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Clinical Programming also provides extensive SAS and database programming support to the RWE team in their Microsoft Azure Databricks environment. More than 13 years of professional experience in pharmaceutical or clinical research.
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Job Introduction: As a Clinical Research Coordinator, you will execute and coordinate a variety of specialized clinical research activities within the Early Phase Clinical Unit (EPCU), ensuring that assigned protocols are executed with high quality, and Standard Operating Procedures (SOPs)and GCP/ICH guidelines are followed.
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Act as the primary contact and provide oversight for all statistical programming related activities outsourced to CROs and external vendors responsible for clinical data analysis deliverables (SAP, CDISC packages, TLFs); ensure quality and timely completion of all clinical data analysis related deliverables.
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Sentara Martha Jefferson Hospital is now hiring a full-time, Clinical Research Nurse. Specialty certification Certified Clinical Research Professional (SOCRA CCRP or ACRP-CP) or Certified Clinical Research Coordinator (CCRC) is required within 3 years of employment.
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clinical research programming jobs Company: J Family Of Companies
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