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Clinical Trial Management Services

The clinical trial management course is available in our training center, we guide throughout the course. The clinical trial course near me helps the aspirants to work as in the research and development field. We provide clinical trial associate training online free for the medical professionals to work in the healthcare industries. Our coaching center offers fine training and allows the candidates to work better in future. The interested students can use this opportunity to build up their career in a better way.

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Clinical Trial Management Services

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  1. Resolve Medicode Clinical Trial Management Services

  2. INTRODUCTION We provide specialized knowledge to the Pharmaceutical, Biotech and Healthcare industries. Our services can be utilized to handle a multitude of complex computational challenges faced by Pharmaceutical, Biotech and Healthcare companies.

  3. CLINICAL TRIAL MANAGEMENT SERVICES If you are looking for an expert partner to manage your clinical trial, we are at your service. As a full-service CRO we support you, on all levels and in every step of your clinical research project.

  4. CTMS offers investigators, collaborators and sponsors several benefits, including: Simplify The powerful site and data management tools, including Medidata Rave, automate many of the functions for setting up and managing multi-site clinical trials and complex studies.

  5. Streamline Increased efficiency in data collection, lock down (validation) and analysis shortens the time from, study completion to reporting and publication. CTMS tools reduce the administrative burden for investigators and study team members, creating additional capacity for research projects.

  6. Standardize When completely implemented, CTMS will integrate seamlessly with other Mayo Clinic research and IT systems and facilitate collaboration with industry sponsors, foundations and federal funding agencies.

  7. PROJECT MANAGEMENT When we lead your project, our main concern is to release you from any stress related to the project management. We always keep a strict eye on quality, budget and timeline. We will track and manage predefined metrics, timelines and anticipated trends. We are there to make sure your clinical trial runs smoothly.

  8. What your dedicated project team will do for you? Plan and execute critical milestones for each study. Provide excellent customer service and proactive communication. Oversee day to day activities of all team members. Identify efficiencies and processes to improve your data quality.

  9. SITE MANAGEMENT To manage your site efficiently, we: Properly review the subject’s safety and the site’s adherence to regulations. Maintain regular and proactive communication with all parties, at every stage from start-up to close-out. Function as a primary point of contact during the course of your trial.

  10. SITE SELECTION Choosing the right site is not an easy task. Our team is experienced and well informed and will, go the extra mile to find the site that suits your trial. Right site is a highly productive site, in a suitable geographical location that can efficiently achieve your accrual goals.

  11. Eligibility BA/BS degree with at 3 - 5 years of clinical trial management experience. Advanced degree (MS/PhD/PharmD) with at least 2 years clinical trial management experience. Strong experience in management of CROs and other vendors. Must have strong knowledge of ICH/GCP guidelines.

  12. CONTACT US +91 81484 52460 info@medi-code.in https://medi-code.in +91 75400 52460

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