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MAKE YOURSELF JOB READY WITH CLINIMINDS & THINKi JOB ORIENTED FAST TRACK PROGRAM

ADVANCED POST GRADUATE DIPLOMA IN CLNICAL RESEARCH AND PHARMACOVIGOLANCE with PHARMACOVIGILANCE ORACLE ARGUS SOFTWARE TRAINING – 100% PAST PLACEMENTS WITH LEADING MNCs AND INDIAN COMPANIES.

Duration: 6 weeks; Program Commencement: 27Th January 2015.

Additional SAS training would also be provided.

HAPPY TO SHARE ASSOCHAM BEST CLINICAL RESEARCH INSTITUTE AWARD TO CLINIMINDS BY THE HON'BLE GOVERNOR OF GUJARAT.

This milestone was reached due to our service to Clinical research education and giving our students the best of education and training which makes them most sought by the industry thus providing them with the best of placement opportunities.

REASONS WHY YOU SHOULD JOIN FAST TRACK PROGRAM
• The common opinion amongst students is that there are NO Jobs for freshers ; however, in reality every company is willing to hire freshers with right skill sets.
• With the increase in unemployment of fresh graduates and post graduates, you need professional skills. This would differentiate you from others.
100% Placement Support Guaranteed.
Clinical Research is rapidly growing industry globally with growth rate of over 40% per annum. Sector requires highly specialized and skilled professional workforce, with applied clinical research & pharmacovigilance. Over 50,000 professionals would be required in the next 3 - 4 years. Global industry size is over US $40 billion and in India, industry is expected to touch the turnover of US $2 billion in the next two years.
Clinical Research, Pharmacovigilance Domain &Software Training – In addition to all major Clinical research ,Pharmacovigilance topics on global regulations, aggregate reporting and quality assurance, every student is introduced to the Pharmacovigilance Database as well through a faculty followed by hands on training. Adverse event processing is taught by using dummy clinical cases and spontaneous cases which includes:
• Clinical Research Introduction
• Principles of Pharmacology & Drug Discovery & Development
• Roles & Responsibilities of Key Stakeholders
• Preparations & Planning for Clinical Trials
• Essential Documentation in Clinical Research & Regulatory Submissions

• Case receipt, triage and tracking
• Assessment of case reports for minimum essential criteria, seriousness, causality, expectedness and regulatory authority reporting requirements
• Duplicate check for pre-existing or active cases
• Data entry into the safety database (Argus) - Students are intensively taught about all the screens of the database. They are provided with a variety of cases that gives them clear idea of entering data to various screens.
• Medical coding using MedDRA browser
• Saving and closing the case
• Medically reviewing the case
• Submission of cases
• Deletion of cases.
• Compliance, Auditing & Quality Control in Clinical Research

Advantages of ORACLE ARGUS SAFETY Software and SAS.

• Directly brought from the vendor (ORACLE CLNICAL and ARGUS SAFETY).
• Easy access for students.
• Live training on Software.
• Highly accepted by the industry.
• No separate training is required done along with the course.
• Job focussed skill development professional program.
• Students are ready to work on projects of the industry after completion of the program.
• Candidates who are trained on software are preferred by Employers.
Classes by experienced Faculty :
Ms. Sapna Sharma
Head, Training and Clinical Research Operations
Ms. Sapna Sharma is a clinical Research Professional with 8 yrs of progressive experience (both national and International) working in Pharmaceutical and Contract Research Organization industry. She possesses excellent interpersonal and communication skills along with clarity of fundamentals with perseverance to succeed and zeal to achieve results; excellent team management skills, acquired by working with teams in different parts of the world - APAC (South Korea, Thailand, Vietnam, China, India Philippines, and Indonesia) and EU (United Kingdom, Israel, Poland, Spain, Bulgaria and Hungary).
She also has a broad background in clinical trial management of phase I/ II/ III/ IV drug and device trials, in various indications including the site monitoring and on-site data management and collection. Specialized in patient recruitment activities in India and other APAC countries, meeting client expectations on projects has always been priority agenda of her work during these last years. She brings with her good medical writing skills with publication of Journals, and research papers, along with a book on Clinical Research (under development) and is also an expert in writing protocols and other clinical research related documents.
Dr. Nisha Nair- Dr. Nisha is an experienced pharmacovigilance professional with nearly 7 years of experience having worked with major projects in multinational CROs and pharma companies. She has worked in almost all areas of pharmacovigilance like single case processing, preparation of aggregate reports, medical writing, literature review, narrative writing, setting up end to end pharmacovigilance systems for companies etc including providing pharmacovigilance training for employees. She has extensive experience in conducting training sessions for International & Domestic Teams and an in depth knowledge various regulatory and international agencies and their guidelines. She currently is in charge of the pharmacovigilance and medical writing functions at Thinki.
Accreditation and Certification: Program is accredited and certified by Pharmaceutical Society of India PSI, India and ACCRE-Accreditation Council for Clinical Research Education, USA

Key Regular Employers : Kinapse; Apcer; Quantum; TCS; Cognizant; MMSH; Novartis; Max Neeman; Accenture and many more.

MAKE YOURSELF JOB READY WITH CLINIMINDS &THINKi JOB ORIENTED FAST TRACK PROGRAM

ADVANCED POST GRADUATE DIPLOMA IN CLINICAL RESEARCH ,CLINICLA DATA MANAGEMENT and SAS FAST TRACK PROGRAM with DATA MANAGEMENT SOFTWARE – 100% PAST PLACEMENTS WITH LEADING MNCs AND INDIAN COMPANIES


Duration: 6 weeks; Program Commencement: 27th January 2015

Additional Pharmacovigilance Oracle Argus Safety Software training would be given.

HAPPY TO SHARE ASSOCHAM BEST CLINICAL RESEARCH INSTITUTE AWARD TO CLINIMINDS BY THE HON'BLE GOVERNOR OF GUJARAT.

This milestone was reached due to our service to Clinical research education and giving our students the best of education and training which makes them most sought by the industry thus providing them with the best of placement opportunities.


REASONS WHY YOU SHOULD JOIN INTERSHIP LINKED PROGRAM

• The common opinion amongst students is that there are NO Jobs for fresher; however, in reality every company is willing to hire freshers with right skill sets.

• With the increase in unemployment of fresh graduates and post graduate, you need professional skills. This would differentiate you from others.

100% Placement Support Guaranteed.

Clinical Research is rapidly growing industry globally with growth rate of over 40% per annum. Sector requires highly specialized and skilled professional workforce, with applied clinical research & pharmacovigilance. Over 50,000 professionals would be required in the next 3 - 4 years. Global industry size is over US $40 billion and in India, industry is expected to touch the turnover of US $2 billion in the next two years.


Clinical Data Management (CDM) is an important specialisation in drug development and clinical trials, which leads to generation and management of high-quality, reliable, and statistically sound data from clinical trials. CDM is the process of collection, cleaning, and management of subject data in compliance with regulatory standards. The primary objective of CDM processes is to provide high-quality data by keeping the number of errors and missing data as low as possible and gather maximum data for analysis. To meet this objective; best practices are adopted to ensure that data are complete, reliable, and processed correctly. This has been facilitated by the use of software applications that maintain an audit trail and provide easy identification and resolution of data discrepancies.
As a part of the program you would learn entire clinical trial process and clinical data management activities. Some of the key areas are :
• Clinical Research Introduction
• Principles of Pharmacology & Drug Discovery & Development
• Roles & Responsibilities of Key Stakeholders
• Preparations & Planning for Clinical Trials
• Essential Documentation in Clinical Research & Regulatory Submissions
• Review and finalization of study documents
• Database designing
• Data collection
• CRF tracking
• Data entry
• Data validation
• Discrepancy management
• Medical coding
• Database locking

Using data management software is critical for generating quality and reliable data. Medrio and Oracle Clinical are some of the important softwares used by several companies.

Advantages of ORACLE CLINICAL Software and SAS.

• Directly brought from the vendor (ORACLE CLNICAL and ARGUS SAFETY).
• Easy access for students.
• Live training on Software.
• Highly accepted by the industry.
• No separate training is required done along with the course.
• Job focussed skill development professional program.
• Students are ready to work on projects of the industry after completion of the program.
• Candidates who are trained on software are preferred by Employers.
Classes by experienced Faculty :
Ms. Sapna Sharma
Head, Training and Clinical Research Operations
Ms. Sapna Sharma is a clinical Research Professional with 8 yrs of progressive experience (both national and International) working in Pharmaceutical and Contract Research Organization industry. She possesses excellent interpersonal and communication skills along with clarity of fundamentals with perseverance to succeed and zeal to achieve results; excellent team management skills, acquired by working with teams in different parts of the world - APAC (South Korea, Thailand, Vietnam, China, India,Philippines, and Indonesia) and EU (United Kingdom, Israel, Poland, Spain, Bulgaria and Hungary).
She also has a broad background in clinical trial management of phase I/ II/ III/ IV drug and device trials, in various indications including the site monitoring and on-site data management and collection. Specialized in patient recruitment activities in India and other APAC countries, meeting client expectations on projects has always been priority agenda of her work during these last years. She brings with her good medical writing skills with publication of Journals, and research papers, along with a book on Clinical Research (under development) and is also an expert in writing protocols and other clinical research related documents.
Lead Faculty: Mr. Pinku Hooda – Mr. Hooda has over 12 years of experience in Clinical Data Management on senior level positions. He has worked in several leading data management and pharmaceutical companies in India and US. Pinku would be assisted by several other trainers with extensive experience in clinical data management and clinical research.
Accreditation and Certification: Program is accredited and certified by Pharmaceutical Society of India PSI, India and ACCRE-Accreditation Council for Clinical Research Education, USA

Key Regular Employers : Kinapse; Apcer; Quantum; TCS; Cognizant; MMSH; Novartis; Max Neeman; Accenture and many more.

Cliniminds was established in Year 2004 – Tenet Health Edutech Pvt. Ltd., promoted by team of Industry professionals and academia. Its India’s first skill development institution in life sciences domain to receive Pharmaceutical Society of India (PSI), Accreditation Council for Clinical Research Education (ACCRE U.S.).
Following courses we offer; Advanced Post Graduate Diploma in Pharmacovigilance, Data Management & SAS, Advanced Post Graduate Diploma in Pharmacovigilance & Medical Writing, Post Graduate Diploma in Medical & Scientific Content Writing, Advanced Post Graduate Diploma in Pharmacovigilance.
We offer wide range of skill development clinical research, pharmaceutical and healthcare educational programs and training solutions
Our programs sustained by superior copyright content and faculty with global stand point.
We have national Presence – 15 major cities in India, International Centers: USA ; UK, RUSSIA, UAE
Program content is targeted towards all major global markets and address the global regulatory environment. Overseas students are growing from Americas; Europe; Middle East; Africa and other countries.
Key Clients for Training Workshops and Online Training Programs : Oracle, NIH USA; MSD; Fresenius Kabi, Germany; Dabur; Novartis; Quintiles; Ranbaxy; GSK; Bioserve; Max Healthcare; Johnson & Johnson; Panacea Biotec.
We have trained over 4,000 professionals, with increasing number of international students for online programs from North America, South America, Europe and Middle East.
We have conducted several industry workshops for leading corporates, viz. NIH, MSD (Merck), Novartis, Biocon, Quintiles, Bioserve, Ranbaxy, Panacea, Max Healthcare, Max Neeman, Apollo Hospitals, Fresenius Kabi, Merck & Co., Panacea Biotec, Asian Clinical Trials, and Quintiles.

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