How can pursuing a Masters in Clinical Trial Management benefit your career?

About Clinical Research

Clinical research and clinical trials is a field of medical science, which deals with the test of investigational compounds or molecules on humans. The trials which are carried on humans are known as Clinical trials, and the subsequent research is Clinical Research.

What is Clinical trial management?

Clinical trial management is the focus area of the job, where management of all sorts of activities related to clinical research and trials are carried out. Here mainly the documentation part and the reporting part is handled with care, and full precautions in order to minimize the errors while recording and submitting the documents to the apex body.

Courses in Clinical trial management

A full-time course is available in the clinical trial management, in which Masters in Clinical Trial Management is available which full-time regular course is. Here all the information and knowledge regarding the same is made understandable to the students, as well as recent updates in the industry are made available to the students, during smart classrooms and smart lectures by the trained and educated staff and faculties.

Why Dysmych?

Dysmych is especially focused on this medical science area and has in-house capabilities in order to run the course effectively as well as efficiently. The trained staffs are fully accustomed to the latest and recent updates in the industry. Regarding the same, the curriculum is planned and executed accordingly in order to provide the best in quality education and substance to the students enrolled for the course in Masters in clinical trial management.

What are the unique and key takeaways for the students studying with us ??

The uniqueness of our training and education program is personalized education to each student, through interactive classroom lectures and complete focus on each respective student, in order to groom them perfectly as per the requirements of the industry in the current role. The students would be informed in planned manner the due course of education programs and subsequent lectures on timely basis. Also, personality development and all-around personal development are also one the key take always for the students how so ever enrolls for the course in our esteemed institute.

Students interface and benefits

The course in our institute is planned by the industry experts also the cost-benefit ratio is higher as compared to other institutes in the whole city. Quality is the prime focus with us, rather than choosing the number of educational materials and interactive sessions held in our institute, the perfect match of the industry requirements and grooming of students from the fresh background makes us one of the best choices for carrying out the master’s program with us.About Clinical Research

Clinical research and clinical trials is a field of medical science, which deals with the test of investigational compounds or molecules on humans. The trials which are carried on humans are known as Clinical trials, and the subsequent research is Clinical Research.

What is Clinical trial management?

Clinical trial management is the focus area of the job, where management of all sorts of activities related to clinical research and trials are carried out. Here mainly the documentation part and the reporting part is handled with care, and full precautions in order to minimize the errors while recording and submitting the documents to the apex body.

Courses in Clinical trial management

A full-time course is available in the clinical trial management, in which Masters in Clinical Trial Management is available which full-time regular course is. Here all the information and knowledge regarding the same is made understandable to the students, as well as recent updates in the industry are made available to the students, during smart classrooms and smart lectures by the trained and educated staff and faculties.

Why Dysmych?

Dysmych is especially focused on this medical science area and has in-house capabilities in order to run the course effectively as well as efficiently. The trained staffs are fully accustomed to the latest and recent updates in the industry. Regarding the same, the curriculum is planned and executed accordingly in order to provide the best in quality education and substance to the students enrolled for the course in Masters in clinical trial management.

What are the unique and key takeaways for the students studying with us ??

The uniqueness of our training and education program is personalized education to each student, through interactive classroom lectures and complete focus on each respective student, in order to groom them perfectly as per the requirements of the industry in the current role. The students would be informed in planned manner the due course of education programs and subsequent lectures on timely basis. Also, personality development and all-around personal development are also one the key take always for the students how so ever enrolls for the course in our esteemed institute.

Students interface and benefits

The course in our institute is planned by the industry experts also the cost-benefit ratio is higher as compared to other institutes in the whole city. Quality is the prime focus with us, rather than choosing the number of educational materials and interactive sessions held in our institute, the perfect match of the industry requirements and grooming of students from the fresh background makes us one of the best choices for carrying out the master’s program with us.

Post Graduate Diploma In Clinical Research

Dysmech clinical research is a premier clinical research institute that offers a wide range of courses in clinical research. DCS is UGC recognized institute. Dysmech clinical research is top training institute. The institute has placed many candidates who are a successful clinical researcher and a part of the clinical research industry.

Dysmech Clinical research offers Following courses

• Diploma In Clinical Research
• PG Diploma in clinical research
• Clinical data management

DCS aimed at filling the gap of demand and supply. DCS Drug discovery and development with drug regulatory programs are available for GLP, Clinical Research, Pharmacovigilance, Regulatory Affairs, and Health Economics Outcomes Research.

Students can apply for full-time as well as part-time courses. Dysmech Clinical Services Pvt ltd (DCS) offers Special Classroom on Weekday / Weekend courses Diploma program in Pharmacovigilance with hands-on software training in Argus/ ARISg/ MedDRA in association with Drug Information Association (DIA) and  Internship certificates and Placement Preparation Programme with add on soft skill training exclusively designed for working professionals and student + Drug Information Association (DIA) student chapter. They provide 100 % placement support all over India or outside India, with many other benefits.

About the Courses

Post Graduate Diploma In Clinical Research And Pharmacovigilance

The courses aim to give an in-depth understanding of the clinical research course. It also enhances the quality of human beings.

Course Duration: 1 Year duration course

 Mode of course:

1.       Full-time

2.       Part-time course

Eligibility:

To enter into clinical research, the candidate should have qualified, 12th standard examinations in the science stream, and basically in a combination of physics, chemistry, and biology. A graduation in science stream is a must, like a Bsc. biology, Bsc. Microbiology, or B.Pharmacy, or Bsc. and Msc. in any of them both.

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Placements: On successful completion of clinical research courses candidate gets placement opportunities from Dysmech Clinical Research.



Advance Diploma in Clinical Research Management Syllabus: Clinical research is a growing field that aids in understanding the causes of various diseases and also aims at developing the science to prevent, to diagnose and to cure the same. Advance Diploma in Clinical Research can help professionals grow their careers to greater heights.





Clinical trial processes in emerging markets are also beneficial for the local healthcare system and the economy of the country. Understanding the cause of various diseases and developing science to diagnose and cure diseases. Advance Diploma in Clinical research can help you take your career to the next level of success.



 Course Curriculum

Introduction to Clinical Research

Clinical Data Management

Pharma Regulatory Affairs

Guidelines

Pharma vigilance and pharma regulatory affairs

Introduction to Clinical research course

As the emerging economy like India in the pharmaceutical, clinical research industry is shifting to become clinical research hubs.Check out the diploma in clinical research syllabus.

MODULE 01: GENERAL INTRODUCTION
MODULE 02: EPIDEMIOLOGY & EVIDENCE-BASED MEDICINE
MODULE 03: PHARMACEUTICAL MEDICINE
MODULE 04: THERAPEUTIC AREAS
MODULE 05: ETHICS IN CLINICAL RESEARCH
MODULE 06: ROLES AND RESPONSIBILITIES
MODULE 07: CLINICAL TRIAL PREPARATION
MODULE 08: ESSENTIAL DOCUMENTS AND REGULATORY SUBMISSION
MODULE 09: STUDY START-UP
MODULE 10: CLINICAL TRIALS MONITORING
MODULE 11: COMPLIANCE AND AUDITS
MODULE 12: DATA MANAGEMENT AND BIOSTATISTICS
MODULE 13: REGULATORY AFFAIRS IN CLINICAL RESEARCH
MODULE 14: MEDICAL DEVICE TRIALS
MODULE 15: PROJECT AND VENDOR MANAGEMENT
MODULE 16: FINANCIAL MANAGEMENT OF CLINICAL TRIALS
MODULE 17: PERSONALITY DEVELOPMENT AND COMMUNICATION SKILLS

Clinical research aids the process of development through its activities traversing from the ethics, conduct, management of man and material, data and its analysis and finally the report generation. Seeing the demand and supply gap in skilled Clinical Researchers, where demand is huge and supply very low. The Post-Graduate Diploma in Clinical Research courses will provide you with an in depth knowledge about clinical research courses and enhance your skill to become trained clinical research professional. The Post-Graduate Diploma in clinical research. These courses can also help professionals working in the industry with the knowledge to reach higher position in their career.

Eligibility Criteria

Any degree in Nursing or Allied Health

Any degree in Pharmacy or Pharmaceutical Sciences

Any degree in Medicine                      

 Any degree in Life Science or BioScience

Dysmech clinical research is top clinical research training institute in Pune. If you want to pursue post graduate diploma in clinical research you can contact us. To know more details like course fees visit http://dysmech.com/skilling-entrepreneurship/clinical-research/

What is clinical research training?

As the emerging economy like India in pharmaceutical, clinical research industry is shifting to become clinical research hubs.

MODULE 01: GENERAL INTRODUCTION
MODULE 02: EPIDEMIOLOGY & EVIDENCE-BASED MEDICINE
MODULE 03: PHARMACEUTICAL MEDICINE
MODULE 04: THERAPEUTIC AREAS
MODULE 05: ETHICS IN CLINICAL RESEARCH
MODULE 06: ROLES AND RESPONSIBILITIES
MODULE 07: CLINICAL TRIAL PREPARATION
MODULE 08: ESSENTIAL DOCUMENTS AND REGULATORY SUBMISSION
MODULE 09: STUDY START-UP
MODULE 10: CLINICAL TRIALS MONITORING
MODULE 11: COMPLIANCE AND AUDITS
MODULE 12: DATA MANAGEMENT AND BIOSTATISTICS
MODULE 13: REGULATORY AFFAIRS IN CLINICAL RESEARCH
MODULE 14: MEDICAL DEVICE TRIALS
MODULE 15: PROJECT AND VENDOR MANAGEMENT
MODULE 16: FINANCIAL MANAGEMENT OF CLINICAL TRIALS
MODULE 17: PERSONALITY DEVELOPMENT AND COMMUNICATION SKILLS

 Clinical research aids the process of development through its activities traversing from the ethics, conduct, management of man and material, data and its analysis and finally the report generation. Seeing the demand and supply gap in skilled Clinical Researchers, where demand is huge and supply very low. The Post-Graduate Diploma in Clinical Research courses will provide you with in-depth knowledge about clinical research courses and enhance your skill to become a trained clinical research professionals. The Post-Graduate Diploma in clinical research. These courses can also help professionals working in the industry with the knowledge to reach a higher position in their careers.

·                     Any degree in Nursing or Allied Health

·                     Any degree in Pharmacy or Pharmaceutical Sciences

·                     Any degree in Medicine                      

·                      Any degree in Life Science or BioScience

Dysmech clinical research is the top clinical research training institute in Pune. If you want to pursue post-graduate diploma in clinical research you can contact us. To know more details like course fees visit http://dysmech.com/skilling-entrepreneurship/clinical-research/

Best Clinical Research Institute In Pune

Dysmech Clinical research is the best clinical research institute in Pune which provides 100% placement assistance. The clinical research course is booming in the industry. If you are looking to build a career in the clinical research industry, clinical research is the only wise option for you. The growth of the industry is directly proportional to the vacancies. The government of India runs various campaigns such as Skill Development Program and Make In India are encouraging the clinical research industry in India. India is becoming an innovation hub for clinical research.

DCS aimed at filling the gap of demand and supply. DCS Drug discovery and development programs are available for GLP, Clinical Research, Pharmacovigilance, Regulatory Affairs and Health Economics Outcomes Research.Dysmech Clinical Research offers clinical research courses like post-graduate diploma in clinical research, diploma in clinical research. As a top training institute, we concentrate on training candidates to make them professional clinical researchers. We provide practical as well as technical training to the candidates. After the course, we provide 100% placement assistance to the candidates.

Candidates who have a degree in life sciences or medicine, pharmacy or pharmaceutical sciences with  55% in the industry.

Clinical research Courses provided by Dysmech Clinical Research include the following section. Our clinical research training course includes the following module.

·         Introduction to Clinical Research

·         Drug Regulations & Ethics in Clinical Research.

·         Clinical Trial Documentation, Audits and Inspections.

·         Clinical Data Management An Introduction

Dysemch clinical research provides placement in various domains in the various roles such as in clinical research associate, Clinical Research Coordinator, Drug Safety Associate, Regulatory Affairs Officer, Project Manager, Clinical Data Analyst, Medical Writer. Dysmech clinical research has a booming career opportunities in pharmaceutical companies, clinical data management companies, healthcare companies, hospitals, IT companies in healthcare, Data management organizations.

Best Institutes For Clinical Research Courses In Pune

There are a number of clinical research training institutes but don’t provide 100% placement guarantee. Here is the list of the clinical research institute which provides the candidate's unlimited interview until the candidate gets placed. Here are the best clinical research training institute in Pune

1.   Dysmech Clinical Research

Dysmech Clinical Research is a renowned clinical research institute and offer the top clinical research courses in Pune. This is the best a clinical research institute in Pune They have trained professionals in the industry They are a global clinical research institute and provides PGDM in clinical research and pharmacovigilance, a Diploma in clinical research. Dysmech provides training with practical with 100% placement.

2. Clini India :

CLINI INDIA is a premier Clinical Research Institute in Pune that has rapidly gained a good reputation for excellence through its innovative approach in clinical research

3. Pro Relix

ProRelix Lifesciences Education is a top institute for Clinical Research & Regulatory Affairs. Pro Relix is  an innovative Education Company established to provide the best clinical research services

After completing the clinical research courses there are high job opportunities in the hospital and healthcare industry. The students can also apply to pharmaceutical companies.

You can check the following job opportunities

    • Clinical trial writer

    • Project manager

   • Clinical trial auditor

   • Regulatory Affairs Executive

   • Data Analyst Pharmacovigilance

   • Manager –Safety / Patents

   • Medical & Regulatory officer

  

   • Medical writer

   • Medical Coding

    • Senior CRA

   • clinical data Manager

What Is Regulatory Affairs (RA)?

RA is an industry that oversees how foods, drugs, and medical products are developed, tested, manufactured, marketed, and distributed to certify that they meet regulatory standards for human use. RA department of a pharmaceutical company is responsible for obtaining approval for new pharmaceutical products and ensuring that approval is maintained for as long as the company wants to keep the product on the market. RA professionals are responsible for ensuring manufacturers’ compliance with applicable global legislative and regulatory requirements at each stage of product development. In the drug, medical device, and biologic product industries, these phases include: research and development, clinical trials, regulatory submissions, manufacturing, marketing, distribution, reimbursement, and post-market surveillance. In the food industries, regulatory professionals engage with products, facilities, manufacturing operations, and distributors along the farm-to-fork lifecycle.

These regulatory professionals play a critical role in the development and distribution of medical technological advancements and drugs, disease-free food, improving people’s health and welfare around the world.

What’s the Job Outlook and Market Demand?

As the RA discipline plays an integral role in medicicne, global health, food safety, and medical innovation, it’s no surprise that the job market is growing. In 2016, the U.S. regulatory market experienced a 42 percent increase in job listings and the U.S. Bureau of Labor Statistics estimates the field will continue to grow at an average rate of eight percent until 2026. As new and developing industries become increasingly regulated, the demand for additional and specialized regulatory expertise will increase.

But what do these professionals actually do on a daily basis?

RA officers act as a link between companies and regulatory authorities, ensuring that products are manufactured and distributed in compliance with appropriate legislation. RA specialists are expected to be extremely passionate regarding the safety and efficiency of drugs and medical devices in the health care industry. Their interest for the sector must be deeply grounded into their function. This role demands expertise in a few distinct areas to be able to become successful. The role includes gathering, evaluating, organizing, managing and collating information in a variety of formats/ ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency (MHRA), different regulatory bodies such as the Food and Drug Administration (FDA or USFDA), Health Science Authority or HSA, the Singaporean regulatory agency, European Medicines Agency (EMA) etc. Some major responsibilities of professionals working in regulatory affairs departments are:
– Formulating a drug development strategies
– Providing regulatory consultation
– Conducting gap analysis
– Developing product dossiers and their submission to applicable regulatory agencies
– Communicating with regulatory agencies
– Providing regulatory affairs related training to applicable team members and/or departments

Regulatory Affairs Careers in Clinical Research

Ever since the field of pharmaceutical drug development, manufacturing and marketing became regulated by regulatory agencies such as the US FDA, EMEA, MHRA etc, the area of Regulatory Affairs has opened up new opportunities of employment. The growth of the clinical research industry has pushed this demand for skilled regulatory affairs professionals even further. Regulatory Affairs careers in clinical research are very satisfying and exciting as the regulatory function is vital in making safe and effective healthcare products available worldwide. Roles and responsibilities of regulatory professionals often begin in the research and development phases for each product and continue throughout the product life cycle. Regulatory Affairs professionals keep themselves updated with global and local regulatory policies, procedures and trends. They also maintain understanding of scientific and technical background of healthcare products. Regulatory affairs department adds great value to drug development worldwide by comprehending and interpreting the regulatory environment and suggesting pathways for reducing the time to market.

How much do these RA professionals earn?

An entry-level Regulatory Affairs Specialist with less than 1 year experience can expect to earn an average total compensation (includes tips, bonus, and overtime pay) of ₹307K. An early career Regulatory Affairs Specialist with 1-4 years of experience earns an average total compensation of ₹386K. A mid-career Regulatory Affairs Specialist with 5-9 years of experience earns an average total compensation of ₹615K. An experienced Regulatory Affairs Specialist with 10-19 years of experience earns an average total compensation of ₹808K.

About the course and the programme at Dysmech Clinical Services Pvt Ltd (DCS)

For regulatory affairs careers in clinical research and in the pharmaceutical industry at large one can undergo Advanced and Diploma courses in Regulatory Affairs and Clinical Research courses in Pune. DCS offers 1 year Advanced and Post Graduate Diploma in Clinical Research and Regulatory Affairs. Anyone prefers to be in Clinical research industry and medical profession can undergo for this programme for detailed knowledge on the same. The main intent of the course is to develop clinical research and RA professionals who are equipped with the most relevant and up to date knowledge and skills. Clinical research and RA training programme is practically driven and centered on the tasks expected of a RA professional in the clinical research industry. In this RA training we provide you with the understanding of the global regulatory structure and acquire skills needed for regulatory strategic planning throughout the life cycle.
About DCS

DCS is an educational, training and soft skill development organization. It is the centre for skill and entrepreneurship development in clinical research industry offering excellent platform and knowledge to land into a good company or enterprise and can boost their growth opportunities by availing the benefits of our wide network and contacts across the companies and industries.

Our company provides best and state of art facilities and knowledge sharing platforms which is an exception in the Industry.DCS offers specialized programs with industry exposure in international standards with Drug information Association (DIA) courses in Pune from experts and top professionals of the same industry itself having a rich experience and exposure on the technologies in the Clinical research industry.

You can very well trust in our honest dealings. Join regulatory affair courses in Pune today.

So, when are you, joining??

Check out the details and contact us today to be leader of tomorrow.

Clinical Research And Regulatory Affair Courses-Dysmech Clinical Research

About the course and the programme at Dysmech Clinical Services Pvt Ltd (DCS)

For regulatory affairs careers in clinical research and in the pharmaceutical industry at large one can undergo Advanced and Diploma courses in Regulatory Affairs and Clinical Research courses in Pune. DCS offers a 1-year Advanced and Post Graduate Diploma in Clinical Research and Regulatory Affairs. Anyone who prefers to be in the Clinical Research industry and the medical profession can undergo for this program for detailed knowledge on the same. The main intent of the course is to develop clinical research and RA professionals who are equipped with the most relevant and up to date knowledge and skills. Clinical research and RA training programme are practically driven and centered on the tasks expected of an RA professional in the clinical research industry. In this RA training we provide you with the understanding of the global regulatory structure and acquire skills needed for regulatory strategic planning throughout the life cycle.
About DCS

DCS is an educational, training and soft skill development organization. It is the center for skill and entrepreneurship development in the clinical research industry offering an excellent platform and knowledge to land into a good company or enterprise and can boost their growth opportunities by availing the benefits of our wide network and contacts across the companies and industries.

Our company provides the best and state of art facilities and knowledge sharing platforms which is an exception in the Industry.DCS offers specialized programs with industry exposure in international standards with the Drug Information Association (DIA) courses in Pune from experts and top professionals of the same industry itself had a rich experience and exposure on the technologies in the Clinical research industry.

You can very well trust in our honest dealings. Join regulatory affair courses in Pune today.

So, when are you, joining??

Check out the details and contact us today to be leader of tomorrow.

Clinical Data Management System

What is Clinical data (CDM) System?

Clinical data management is a critical process in clinical research. With the help of software application for CDM process In this, all data from clinical trials are gathered and the record is maintained.

 There are some clinical research training courses that offer the best planning program of clinical data management and the organization of clinical data is set up in clinical research courses. Research training is the best way to enter into the clinical research field.

How Does Clinical Data Management (CDM) Work?

 Clinical data is maintained properly for future purposes. CDM is the process of collection, cleaning and management of subject data in compliance with regulatory standards. There are software applications to keep clinical research data records.

The whole CDM process is designed keeping the deliverable in view. A clinical trial is designed to answer the research question. The CDM process starts early and this process is designed with the aim of delivering error-free, valid and statistically sound data.

What is the eligibility Criteria to apply for clinical research course?

Clinical research refers to all research carried out for the sake of human beings. It focuses on inventing medicines, developing diagnostic methods for better medical care. The invention of medicines leads to better patient care.

 Dysmech Clinical Research offers the best clinical research courses in Pune with a 100% job guarantee. In the clinical research industry, the syllabus of clinical research courses in Dysmech clinical research is designed by corporate experts. There are many clinical research institute but they provide 100% assistance. They can work as Clinical research associates, clinical Clinical research managers, clinical data managers.

Clinical research refers to all research carried out for the sake of human beings. It focuses on inventing medicines, developing diagnostic methods for better medical care. The invention of medicines leads to better patient care.

Dysmech Clinical Research offers the best clinical research courses in Pune with a 100% job guarantee. In the clinical research industry, the syllabus of clinical research courses in Dysmech clinical research is designed by corporate experts. There are many clinical research institute but they provide 100% assistance. They can work as Clinical research associates, clinical Clinical research managers, clinical data managers.

http://dysmech.com/skilling-entrepreneurship/clinical-research/

Our training programs give equal importance to both technical knowledge and practical case studies. Our training institute help candidates become trained and qualified clinical professional. There are many clinical research institute that provides clinical research courses with 100% assistance after the course. But Dysmech Clinical Research provides 100% placement to the students.

Clinical Research Course Eligibility & Duration:

The duration of clinical research courses at Dysmech Clinical Research is 4 months. Candidates should have a minimum of 55% in his graduation. Candidates holding the following degrees are eligible to apply for this course:\

Course Duration 

6 months-1 year

 Who can apply for a clinical researcher posts?

A person having a degree in the following domain can apply for the post.

Any degree in Nursing or Allied Health

Any degree in Pharmacy or Pharmaceutical Sciences

Any degree in Medicine

 Any degree in Life Science or BioScience

WHERE CAN YOU APPLY FOR PHARMACOVIGILANCE COURSES IN PUNE?

What is Pharmacovigilance?

Pharmacovigilance is a branch of the pharmacy where vigilance is kept over the use of drugs. According to WHO guidelines, proper reporting of Adverse drug reactions, and Adverse events is necessary in order to completely justify the job of Pharmacovigilance. At present career in it is at boom and various institutes provide Pharmacovigilance courses.

Duties of Pharmacovigilance…

The Pharmacovigilance officers carry out a complete survey and report of ADR’S and AE’S regarding the drugs and their classifications during the whole course of the year and complete their job of reporting by filling up the forms online and submitting them to FDA and WHO. The scope of it and growth opportunities in its field are wide and are presently at boom citing the needs and requirements of the industry.  A lot of colleges and private institutes provide clinical research and Pharmacovigilance courses, however, the course provided by our institute, is at par with the current industry requirements and recent updates that are happening and followed across the world.

About the courses…

Students doing clinical research and Pharmacovigilance courses from our institute would have excellent platform and knowledge to land into a good company or enterprise and can boost their growth opportunities and avail the benefits of our wide network and contacts we hold in the industry looking at the present scenario. Compared to pan India, the Pharmacovigilance courses in Pune are one of the best in industry and the knowledge delivering and sharing practices are one of the best in the country.

Courses in it are either provided in combination or are also available separately in order to justify the requirements of the students and their career plans in this field of science. Looking at the growing demand for the courses, our institute has introduced the state of the art curriculum which will help our students to cope with the requirements and pressures of the real job.

About DCS Institute…

Our Institute provides the best and state of art facilities and knowledge sharing platforms which is an exception in the Pharmacovigilance courses in Pune. For more details click here website.