Clinical Trial Management Services

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Resolve Medicode
Clinical Trial Management Services
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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SITE MANAGEMENT
To manage your site efficiently, we
Properly review the subjects safety and the
sites 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.
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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.
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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.
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CONTACT US
91 81484 52460
info_at_medi-code.in
https//medi-code.in
91 75400 52460