Novella Clinical | Specialty Oncology and Medical Device CRO - Novella Clinical is a full-service CRO focused on the unique needs of small to mid-sized oncology companies and medical device and diagnostics companies.

  • Specialty Oncology CRO - Novella Clinical - Novella Clinical is a specialty oncology CRO with highly experienced oncology staff, a flexible service model and global footprint.
  • Oncology Experience | Global CRO | More than 50 Countries - As a full service, global CRO, we have the indication-specific oncology experience to effectively guide your drug through clinical trial.
  • Hematology Oncology Trial Experience - Novella Clinical - Novella Clinical understands hematologic oncology trials are fundamentally different from solid tumor studies. Learn more.
  • Immunotherapy Clinical Research - Advance your immunotherapy drug development program with access to Novella Clinical's vast immunotherapy clinical research experience.
  • Specialty Oncology CRO Services - Novella Clinical - Novella’s specialty Oncology services are here to help move your oncology products to market and into the hands of patients who need them most.
  • Project Management - Novella Clinical - Novella Clinical’s dedicated oncology Project Management teams excel in navigating the cancer drug development process.
  • Clinical Monitoring - Novella Clinical - We utilize a clinical monitoring model based on one principle: our global oncology CRAs are assigned based on oncology experience (tumor type) and location.
  • Data Management - Novella Clinical - With Novella, you benefit from our eClinical heritage that gives us the experience to provide targeted data management solutions for each study.
  • Data Monitoring Committees - Novella Clinical - Novella offers our customers the necessary expertise for the successful implementation of Data Monitoring Committees
  • Investigator Strategy - Novella Clinical - Our Investigator Strategy & Site Coordination team uses a multifaceted approach to produce precise representation of clinical environments for trials.
  • Safety and Pharmacovigilance - Novella Clinical - Our safety and pharmacovigilance team uses the latest safety processes; lowering risk associated with storing documents across multiple locations.
  • Medical Monitoring - Novella Clinical - Novella Clinical’s Medical Monitoring department employs a core group of licensed and board-certified, in-house clinical research physicians.
  • Medical Writing - Novella Clinical - We understand the importance of medical writing from protocol to package insert. Our goal is to produce concise, substantive, polished clinical documents.
  • Regulatory Affairs for Oncology Trials - Novella Clinical - Our Regulatory Affairs team is experienced in working with domestic and international agencies as well as IRB/ethics committees.
  • Quality Assurance - Novella Clinical - Our independent Quality Assurance (QA) department performs regular quality assessments of our services to ensure compliance.
  • Steering Committees and Clinical Advisory Boards - Novella Clinical - Novella offers the necessary expertise for the successful implementation of Clinical Advisory Boards, Executive Committees and Steering Committees.
  • Training oncology research professionals - Novella Clinical - Novella Clinical’s Training department has instructed over 17,000 clinical research professionals and supported 4,500+ investigative sites.
  • Oncology Clinical Staffing - Novella Clinical - As staffing experts, via Novella Clinical Resourcing, we have placed experienced oncology professionals in both short and long-term assignments since 2005
  • Oncology Trials Resources - Novella Clinical - Novella Clinical provides oncology trials resources through white papers, webinars and fact sheets. Learn more.
  • The Promise of Liquid Biopsy Technology - Novella Clinical - This white paper explores the potential of liquid biopsy technology and it's ability to change the path of oncology research and treatment. Learn more.
  • Medical Device CRO | Global Reach | Novella Clinical - As a specialty medical device CRO, we concentrate on the unique needs of medical device and diagnostics companies to guide your trial to success.
  • Medical Device Experience that Counts - As a full-service, global CRO we have the medical device experience to understand the intricacies and nuances of your clinical device trial.
  • Cardiovascular Device CRO Experience - Novella Clinical - Advance your cardiovascular medical device clinical research program with access to world-class cardiologists from a leading Cardiovascular Device CRO.
  • In Vitro Diagnostics - Novella Clinical - Novella’s Diagnostics team offers specific experience in regulatory consulting, design and execution of in vitro diagnostics (IVD) clinical studies
  • Medical Device Trial Services - Novella Clinical - Novella’s dedicated Medical Device & Diagnostics Division offers a broad range of clinical trial management services from preclinical to post-approval.
  • Project Management - Novella Clinical - Project Management is at the center of good clinical trial work. Novella Clinical’s dedicated medical device team plan and execute critical milestones
  • Clinical Monitoring - Novella Clinical - Novella Clinical utilizes a clinical monitoring model based on one simple principle: every CRA is assigned based on specific experience and location
  • Data Management - Novella Clinical - With Novella, you benefit from our eClinical heritage that gives us the experience to provide targeted data management solutions for each study – with a focus on quality
  • Data Monitoring Committees - Novella Clinical - Novella offers our customers the necessary expertise for the successful implementation of Data Monitoring Committees.
  • Clinical Events Committee - Novella Clinical - CEC adjudication provides a standard, systematic and unbiased assessment of endpoints to determine whether they meet protocol-specified criteria.

    Country:, North America, US

    City: -98.3987 Texas, United States

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