Do you want to get jobs (FRESHERS) in Clinical Research/ Pharmacovigilance? - Click for more details "D"

Clinical Trial Management

A Clinical Research is a systematic study for new drugs in human subjects to generate data for discovering or verifying the Clinical, Pharmacological (including pharmacodynamics and pharmacokinetic) or adverse Effects with the objective of determining safety and efficacy of the new drug.

Clinical Research Industry has grown around the world at an unparalleled rate in the past few years. It has opened up new vistas of employment for a large number of people. The Clinical Trials market worldwide is worth over US$ 45 billion and the industry has employed an estimated 2,10,000 people in the US and over 70,000 people in the UK and they form one third of the total Research and Development staff. These large numbers can be attributed to the fact that this industry offers lucrative employment opportunities. The average nominal annual salary growth across all the positions is 4% as against less than 1% for other segments.

Work Profile:

• Clinical Research Coordinator (CRC)
• Clinical Research Associate

Clinical Research Coordinator (CRC)

The Clinical Research Coordinator (CRC) is responsible for conducting clinical trials using good clinical practice (GCP) under the auspices of the Principal Investigator (PI).

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• All trials are conducted ethically, as defined by the Declaration of Helsinki, rigorously, as defined by the International Conference on Harmonization Guidelines (ICH).
• Benefits outweigh risks for each patient.
• Rights, safety and well-being of patients prevail over science.
• All available non-clinical and clinical information on any investigational agent can support the trial as designed.
• All trials are scientifically sound and clearly described.
• All clinical trials have current Institutional Review Board approval.
• Medical decisions and care are the responsibility of qualified health care professionals, specifically physicians and, if applicable, dentists.
• Everyone involved in the clinical trial is qualified by training, education and experience.
• Informed consent is given freely by every participant.
• All study documentation is recorded, handled and stored to allow accurate reporting, interpretation and verification.
• Confidentiality of subjects is respected and protected.
• Investigational products maintain Good Manufacturing Practice in storage, manufacturing and handling.
• Systems to ensure quality are implemented in all aspects of the trial.

- See more at: http://www.cliniindia.com/clinical-trial-management/#sthash.dFomAIUj.dpuf

Clinical Data Management

India has developed into a super power for IT skills and has become a major hub for pharmaceutical and biotech manufacturing and contract research, the outsourcing business in various other segments is also exhibiting promise. Clinical trial data management and statistical analysis is one such area which is growing rapidly, accompanied by a variety of players entering into different models of this business. The author reflects on the data management business in India and reviews the emerging outsourcing models in this growing industry. He has also attempted to work out a break-even analysis considering the projected investment on high quality and costly infrastructure like; hardware, software and human resources to augment the business and regulatory requirements of the industry.

Work Profile

Clinical Data Analyst/ Manager

Job Description

Primary responsibility is to ensure the validity of clinical trial data and format them for statistical purposes. Also designs collection instruments, sets up databases and tracks and manages the flow of data to and from the investigative sites. With supervision, establishes protocol-specific data review and entry guidelines to document data validation and formatting procedures and defines batch-ending programs. Monitors timely data entry. Reviews data discrepancies resolutions provided by the investigative sites and enters corrections in the database, as appropriate. Assists in the review of interim/final data listings prior to transmission to other groups or inclusion in interim/final reports. Is familiar with database management systems and the principles, organization and content of standard Case Report Form (CRF) libraries. Ensures that incoming CRFs are tracked in a timely manner prior to safety review and upon manual review. Is familiar with data coding of Standard Operating Practices (SOP) and coding dictionaries. Conducts database audits according to established SOPs and is familiar with the implementation of GCPs.

- See more at: http://www.cliniindia.com/clinical-data-management/#sthash.gXOLZ4ls.dpuf

Pharmacovigilance

Pharmacovigilance is the pharmacological science relating to the detection, assessment, understanding and prevention of adverse effects, particularly long term and short term side effects of medicines. In general, Pharmacovigilance is the science of collecting, monitoring, researching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications, biological products, herbalism and traditional medicines with a view to: identifying new information about hazards associated with medicines preventing harm to patients. Pharmacovigilance is particularly concerned with adverse drug reactions, or ADRs, which are officially described as: “A response to a drug which is noxious and unintended, and which occurs at doses normally use for the prophylaxis, diagnosis or therapy of disease, or for the modification of physiological function.

Work Profile

Drug Safety Associate Responsibilities / Case Processing Expert/ Pharmacovigilance Associate

Job Description:

Drug Safety Associate manage activities relating to the collection, processing, follow-up, analysis, and regulatory reporting of adverse events (AEs) and serious adverse events (SAEs) for marketed products and investigational products.

The DSA ensures timely submission of reports regulatory agencies in accordance with applicable regulations and that all inquiries from the FDA and other drug regulatory agencies are responded to in a timely manner. The DSA will respond to inquiries from health care professionals, consumers, and company personnel regarding safety issues with marketed products; prepare periodic comprehensive written reviews of all assigned AEs; identify potential sources of product litigation, extract AE data from various clinical trial cases and spontaneous sources; manage case-related information including interpretation of medical conditions, lab results, and procedures as well as compile complete narrative summaries; and ensure proper coding (MedDRA) into the global AE database.

 Who hires Pharmacovigilance Professionals?

People trained in Pharmacovigilance can find excellent work opportunities in following organizations:

• Pharma-Companies ( Novartis, Dr. Reddys, Ranbaxy etc)
• Contract Research Organizations (CROs)
• Biotech companies.
• IT Companies like Accenture, TCS, Cognizant, Wipro, Mahindra Satyam etc
• Regulatory Authorities such as DCG(I), FDA & CDSCO

- See more at: http://www.cliniindia.com/pharmacovigilance/#sthash.PGxHOPGN.dpuf

Medical Writing

Medical writing is the activity of producing scientific documentation by a specialized writer. The medical writer typically is not one of the scientists or doctors who performed the research. A medical writer, working with doctors, scientists, and other subject matter experts, creates documents that effectively and clearly describe research results, product use and other medical information. The medical writer also makes sure the documents comply with regulatory, journal, or other guidelines in terms of content, format and structure. Medical writing as a function became established in the pharmaceutical world because the industry recognized it requires special skill to produce well-structured documents that present information clearly and concisely. A growing number of new drugs go through the increasingly complex process of clinical trials and regulatory procedures that lead to market approval. This drives a demand for well written, standards-compliant documents that science professionals can read and understand easily and quickly.

Work Profile

Medical Writer/ Content Writer/ Medical Data Reviewer

Job Description
Responsible for the timely preparation, production and quality control of regulatory documents, including coordinating with regulatory project teams, creating editorial timelines and work flow specifications, scheduling and tracking documents, assessing documentation staffing needs, participating in “round-table” review of documents, establishing project-specific style guidelines, editing at various levels, writing and proofreading. Develops and updates specifications for the design, format production elements, tracking of regulatory documents and artwork used in regulatory documents. Hires, trains and supervises editorial temporaries and coordinates their work. Develops and updates departmental editorial style standards by preparing and revising a style guide. Provides guidance on writing to authors of regulatory submissions, and develops and updates general writing guidelines by preparing and revising an author’s guide.

- See more at: http://www.cliniindia.com/medical-writing/#sthash.eLX5CZ3F.dpuf

Regulatory Affairs

Pharma regulatory affairs professionals play an essential role in ensuring all pharmaceutical products comply with regulations governing the industry.

The regulatory function in healthcare industries is vital in making safe and effective healthcare products available worldwide. Individuals who ensure regulatory compliance and prepare submissions, as well as those whose main job function is clinical affairs or quality assurance are all considered regulatory professionals.

Regulatory professionals are employed in industry, government and academia and are involved with a wide range of products, including:

• pharmaceuticals
• Medical devices
• In vitro diagnostics
• Biologics and biotechnology
• Nutritional products
• Cosmetics
• Veterinary products

The regulatory professional’s roles and responsibilities often begin in the research and development phases, moving into clinical trials and extending through premarket approvals, manufacturing, labeling and advertising and post market surveillance.

Work Profile

Regulatory Affairs Associate

Job Description
Ensures all company products meet worldwide regulatory requirements by supporting all assigned regulatory aspects of product approval and post-marketing compliance. Responsible for the coordination and preparation of document packages for regulatory submissions ensuring compliance with the Food and Drug Administration (FDA) and international regulations/ interpretations. This may include the review, evaluation, and compilation of files and reports for submissions. Provides project team representation and direction in managing information from/to other departments (including R&D, Manufacturing, Quality Assurance, Quality Control, Medical Affairs, Marketing, and Clinical Affairs) regarding Regulatory submissions.

This may include the preparation of outlines, summaries, status reports, graphs, charts, tables and slides for distribution and communication to other departments. Reviews technical and clinical documentation and recommends changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. Researches and analyzes regulatory information and determines acceptability of data, procedures, and other product-related documentation presented in support of product registration. Is responsible for the timely completion of regulatory projects and submission of documentation to regulatory agencies. Develops and maintains current regulatory knowledge and keeps abreast of regulatory procedures and changes. May provide regulatory guidance to project teams and junior staff.

- See more at: http://www.cliniindia.com/regulatory-affairs/#sthash.E4Au9HPu.dpuf

"CALL @ 092 898 70004/ 080 -004 - 0004 (OFFICE TIME) For any Query"

Grab excellence !! On this Independence Day!!!! Clini India wishes you all a very Happy Independence Day 2015.

Happy 69th Independence Day Clini India wishes you all a very Happy Independence Day 2015.  India is growing at a very fast pace but student community in India still haven't received complete freedom. Get freedom from your Job search Get freedom from your Unemployment tag Get freedom from your Career frustration If you are dreaming for your freedom, then we are there to fight with you. Join hands with Clini India and receive real freedom. Join this movement of Clini India and be Independent.   Facebook Website Job Portal

OPENINGS FOR EXPERIENCED CANDIDATES IN TCS MUMBAI

Company Profile:

Tata Consultancy Services Ltd.

TCS as an Organization are pioneers in BPS services. This key strategic division - powered by a unique combination of deep domain expertise, process excellence and innovative technology world-class solutions across diverse industries. With a talent pool of over 67000 BPS has state-of-the-art delivery centers spread across India, Hungary, Ecuador, Chile, Uruguay, UK, SA and China.

POSTS:

1》Aggregate Reporting Scientist
B.Pharm/M.Pharm/BAMS/BHMS/BDS/BPT
1-6 yrs experience

2》Regulatory affairs
B.Pharm/M.Sc Graduates
1-3 yrs experience

Send ur CV on chavan.mahesh1@tcs.com

Date-29/July/2015
Time-11am-4pm
Venue-TCS WellSpring, Plant No.12, Godrej & Boyce complex, LBS Marg, Vikhroli, Mumbai-400079

FRESHERS OPENINGS FOR PHARMACOVIGILANCE @ NOVO NORDISK

 Walk in by Novo Nordisk for Pharmacovigilance domain for Bangalore location (only for freshers).

Date of interview: 11 and 12 Aug 2015

Location: ITC Maratha, Andheri, Mumbai

Package: 3.75 lacs to 4 lacs per annum

Qualification: B. Pharm and M.Phram

Kindly forward your CVs to rlma@novonordisk.com and vdsz@novonordisk.com

There will not be any reimbursement from Novo Nordisk for attending interviews.

Opening for Scientist - Molecular Biology PCR Amplification @ Manipal Acunova "B"

Opening for Scientist - Molecular Biology PCR Amplification @ Manipal Acunova
 
Ecron Acunova provides end-to-end services for Phase I - IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab. Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. As regional experts, we operate each region as a priority market. Our European HQ is in Frankfurt, Germany, in the United States our HQ is in Princeton, NJ and our Asian HQ is in Bangalore, India. We offer clinical development services to the pharmaceutical, biotechnology, nutritional, device and medical diagnostics industries. Our service quality, therapeutic expertise and global reach have allowed us to grow rapidly, building a list of demanding clients. We provide an attractive package of services coupled with the ability to rapidly conduct clinical trials utilizing a world class delivery platform.

Job Title : Scientist - Molecular Biology PCR Amplification

Eligibility : B.sc/M.sc Bicohemistry/ Microbiology / Biotechnology / Life science

Experience : 0-2 years

Job Description :

Registering the samples, analysing samples, result entry,
Filing maintenance of records, maintenance of instruments, stock maintenance in the department, calibration of instruments, maintenance of all records- instrument printouts, QC logs, personal training in PCR/ AMD
Serology, Microbiology, Clinical Biochemistry, Hematology and Clinical Pathology sections.
All the activities shall be carried out under supervision of HOD or designee

How To apply : Intersted Candidates send their resumes @ careers-asia@ecronacunova.com

Opportunity for Life Science / Clinical research candidates as Clinical Data Analyst @ PAREXEL "B"

Opportunity for Life Science / Clinical research candidates  as Clinical Data Analyst @ PAREXEL



For over 30 years, PAREXEL has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. We’re also an astute guide, able to simplify that journey for our clients, so safe new products can reach patients more quickly. PAREXEL strives to be the premier provider to the biopharmaceutical and medical device industries for the development and commercialization of new medical therapies worldwide.PAREXEL's mission is to combine the strength of our expertise, experience and innovation to advance the worldwide success of the biopharmaceutical and medical device industries in preventing and curing disease.

Job Title : Clinical Data Analyst

Eligibility : B.sc/M.sc Life science/ Clinical Research

Experience : 1-2 years

Job Description :

The role of the Clinical Data Analyst (CDA) is to perform all clinical data cleaning activities on assigned projects, commensurate with experience and/or project role. Key activities include data validation, generation and integration of queries, coding of clinical data, reconciliation of safety and electronic data.
Click here to apply

Opening for Safety Aggregate Reporting and Analytics (sara) @ Quintiles

Opening for Safety Aggregate Reporting and Analytics (sara) @ Quintiles

Dear Candidate,

Opening for experienced candidates for SARA with 4+ years of relevant experience.

Quintiles is the worlds leading provider of biopharmaceutical services. With a network of 29,000 employees conducting business in approximately 100 countries, Quintiles has helped develop or commercialize all of 2013s top 100 best-selling products or compounds. Using our extensive therapeutic, scientific and analytics expertise, we help biopharmaceutical and health sciences customers navigate the increasingly complex landscape with more predictability to enable better outcomes.

RESPONSIBILITIES
Comply with all applicable service level agreements for SARA deliverables.
Serve as principal owner of the SARA deliverable and have responsiblility for completion of the document in compliance with all applicable service level agreement s.
Prepare each version of the Safety Aggregate Reporting and Analytics deliverable and maintain version control of the document. Request source documents from other Quintiles departments or customers. May also request example documents, style guide and other documents (e.g., signal analyses, regulatory correspondence) as deemed necessary. Address all review comments by both internal and external stakeholders.
Attend internal and customer project team meetings (face-to-face, online or via teleconference) as defined in the scope of work (SOW) and budget. Attend planning meetings, data interpretation meetings, online documents review meetings, as required.
Perform delegated lead activites with supervision. Lead small projects and ensure all activites are completed on time and meet quality standards
Mentor less experienced or newer staff members.
Work closely with case processing service operations to resolve issues, if any.
Interface with other functional groups, such as Regulatory Affairs, Clinical/Medical Affairs functions, Quality, Information Technology, or other business units as needed
Assist in preparation of function-specific responses to regulatory authority requests and of function-specific responses to assessment reports from regulatory authorities, if required
Lead or participate in project teams and committees as assigned. Initiate new projects to improve processes
Contribute to achievement of departmental goals e.g. utilization realization and productivity metrics.
Read and acknowledge all necessary Quintiles standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Work towards ensuring your individual training plan and training transcript are reconcilable.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Excellent knowledge of One Q Safety services and processes; willingness and aptitude to learn new skills across One Q Safety service lines.
Good understanding of applicable global, regional, local clinical research regulatory requirements; i.e. Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP),and International Conference of Harmonization (ICH) guidelines, Standard Operating procedures (SOPs)
Proven ability to meet strict deadlines; manage competing priorities and changing demands.
Proven ability to follow instructions/guidelines, work independently and on own initiative.
Good understanding of operational metrics, productivity and initiatives.
Excellent attention to detail and accuracy and maintain consistently high quality standards.
Effective mentoring skills.
Excellent written and verbal communication and report writing skills.
Ability to be flexible and receptive to changing process demands.
Sound judgment; decision making skills.
Ability to work effectively on multiple projects simultaneously. Organize own workload and effectively time manage competing priorities.

Click here to apply

Opening for Patient Care Advisor @ Indegene LifeSystems Pvt Ltd

Opening for Patient Care Advisor @ Indegene LifeSystems Pvt Ltd

Job Description
Meeting with 4 - 5 patients suffering from different ailments everyday (at the hospitals, clinics, homes if required)
Counseling and speaking to them for health outcomes management in person so that they understand the long-term implications of managed patient care

Collate health records related data from consenting patients

Meet the regular patients at regular intervals as advised

Capture details related to Adverse Drug Reactions reported by patient in pre-defined templates

Handling patient queries and providing response from pre-defined FAQs

Provide patient support by coordinating with pharmacists and stockists

Receive regular feedback from team managers and undergo program related training and on the job training on a regular basis



Skills Required



Qualifications: B.Pharm/ B.Sc (Microbiology, Biotechnology, Dietics, Nutrition) fresher – 2 years of experience.

Fluent in English, Hindi and any one regional language (Gujarati, Marathi, Bengali, Kannada, Tamil, Telugu and Malayalam, Assamese, Rajasthani)

Good computer skills

Ability to work in a process driven/ structured environment

Empathy and willingness to listen and relate.

Candidates with two Wheeler are preferred.
Salary: Not Disclosed by Recruiter
Industry:Medical / Healthcare / Hospitals
Functional Area:Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology
Role Category:Medical Professional
Role:Medical Officer
Desired Candidate Profile
Education-
UG: B.Pharma
PG:Post Graduation Not Required
Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required
Please refer to the Job description above
Company Profile:
Indegene LifeSystems Pvt Ltd

Click here to apply

CLINI INDIA Tribute to our Ex- President Abdul Kalam -Let's salute him: 14 Realistic Quotes For Your Life

Abdul Kalam : 14 Realistic Quotes For Your Life

A sad loss

It is a sad thing to look at the news channels today to see that one of the most inspiring men india has ever seen is no more. The man and his achievements speak for themselves. It has always been a delight to hear his speeches, read about him. The spark in him has ignited so many minds that it is impossible to pay a true homage to such a personality.

Having said that, a personality might pass but his thoughts, principles and ideas live long, live so long that they become parts of our personality and our thoughts. What better respect can we give this man than living up to the ideals he shared and helped us rethink our lives in a fresher way. Its a sad loss today but the man lives along, in you, in me and in us. Here is a collection of his powerful quotes and their meaning, interpretation for our lives.

Abdul Kalam : The Missile Man Of India

Abdul Kalam, the scientist, president, an aerospace Engineer – popularly called the Missile Man of India is no wonder an inspiration to millions of Indians spread across the world. The winner of Bharat Ratna – India’s highest civilian honor is most popular for his interaction with the student community. I guess there are very few people who retain the child in them as they grow. Here is one man who has grown not inspite of the child like qualities but because of them. Here is a collection of 15 realistic quotes from Abdul Kalam. 

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Dream, Dream Dream, Dreams transform into thoughts and thoughts result in action.

It is very conflicting when someone uses the word dreams – they seem to be so cliched these days – especially with the amount of fantasy added to them. Having said that, I would be foolish to look at the idea of a dream lightly.

It was the dream of the wright brothers which make us fly today, it was the dream of cavemen which made us enjoy cooked food. I am sure at some point every little thing we do today might have felt unreasonably impossible for someone else generations together and they would have killed to have what we do today.

Maybe it makes sense to appreciate that and look at our dreams a little closer for these are the very precious ones which define us, enable us and push us to make them come true. For we all are here for that one dream – the dream to make our opportunities and our lives count! And before we part to the next quote, we leave you with a question – Are you living your childhood dreams?

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Dreams are not those which comes while we are sleeping, but dreams are those when u don’t sleep before fulfilling them.

There sure seems to be a lot of misconception when it comes to dream. And somehow in the parlance dreams seem to have taken a backstage, playing a lighter role.

But truth is – a dream is much more than that. As kalam says – it is not those dreams which make us dormant that count. We keep having those everyday and we don’t even remember most of them. But there are those few things which really define us – make us realize who we are really passionate about and what we are willing to stand up for.

Those are the real dreams and they deserve every little thing we can afford to make them come true. And here are the top 10 reasons we should avoid to chase our dreams and make them a reality. 

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This is my belief: that through difficulties and problems God gives us the opportunity to grow. So when your hopes and dreams and goals are dashed, search among the wreckage, you may find a golden opportunity hidden in the ruins.

We all hate our difficulties and challenges. I haven’t met many people who are excited at the sight of trouble, and I am no different either. But beyond all these challenges – there is a hidden message, sometimes a test to see how badly you want something and sometimes just a signal to alter the route you have followed so far.

But it is true that each of these challenges come with a purpose -a single purpose to help you achieve and realize your destiny. We can either let them have a strong impact on us, be completely overwhelmed by them and stop.

Or – We can stand our ground – tell ourselves or rather prove to ourselves that we are stronger than these challenges and like kalam says – give ourselves an opportunity to identify the gold hidden in the ruins.

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Difficulties in your life do not come to destroy you, but to help you realize your hidden potential and power, let difficulties know that you too are difficult.

This quote seems very similar to the one above depicting the reason, purpose and the path for these difficulties in life. They either make us or break us – this is what most people are going to tell you.

But difficulties alone don’t make us or break us – it is simply us who do that. We define what those difficulties mean to us. We define how much impact they are going to have on our lives and we alone determine the course these difficulties take.

We can do the easier action of finding someone to blame it on – most times it is Luck, the theologists say it is god while the fatalists say it is fate. But a simple man says – it is an aberration and we need to find a way around it. What do you think?

In the end tougher challenges simply make you better! 

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All birds find shelter during a rain. But Eagles avoid rain by flying above the clouds. Problems are common, but attitude make the difference.

Every one of us faces problems in life and each of these problems are unique in their own way – their appearance, impact and the solutions too.

We all face these 6 confusing quests to solve our troubles in life – Denial, Anger, Solutions, Conflicts and so much more. But we need to order these quests to benefit us the most so that we find the best way out of the problem.

As Kalam says – The majestic eagle finds its way to the top of the clouds. So if you want a solution similar to the eagle you must ask the eagle. The sparrow can only advice you to hide and even if it asks you to cross over the clouds you would rarely want to believe a sparrow cos it has never done it. In other words the sparrow lacks credibility.

So, be careful about who you go to for advice. There are the 6 peculiar people who advice you, but only you get to decide what you do with the advice. Some of it needs to be taken seriously, and some – not at all. Be clever – be the master of your own destiny.

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Failure will never overtake me if my definition to succeed is strong enough.

Ask every underachiever in life the reason behind his failure. Most of them seem to have some excellent stories. As Jordan Belfort says – “The only thing standing between you and your success is the bullshit story as to why you can’t have it”.

We need to realize this one truth – No one really cares why you didn’t do something. The reasons we give are not a justification for anyone else but ourselves and we tend to delve hours together on it to formulate these reasons.

But we need to step out of it, take a wider look at it – the answer is very simple – we just need to ask the right question. And the question is –

Do you really want it? 

How badly do you want it? 

What are you willing to do for it? 

Your answer to this determines your next course of action and the result of whether it is a success or a failure. And here are 10 inspiring failure quotes for your life

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Thinking is the capital, Enterprise is the way, and Hard Work is the solution.

Well these are the simple 3 steps to solve any problem you might have in life – Thinking, Finding innovative solutions and working towards the solution.

Everything else is either a detour around these steps or sometimes even a distraction.

One of the strongest challenges for success is that sometimes we have too many steps between the success and failure. In other words the path is too long and tedious which makes success harder to achieve.

Keep it really simple – keep it to these simple  steps kalam advises and you might find a simple way out of your problems.

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Suffering is the essence of success!

Does it remind you of this quote – Pain is essential but suffering is optional?!

I like the quote – it is rebellious, it is the ultimate belief in human will. But I am a simple man – I am not evolved enough not to feel anything. There are too many conflicts in my mind and I don’t find it that wrong at all.

But maybe we are looking at it all wrong. We don’t have to try and define everything in life – pain or suffering is a great motivator. We just need to learn how to channel it to bring out the best in us.

We would have remained at the same emotional state we were years ago if it were not for the pain or suffering we went through. They changed us as people, someone we are today. We might be proud or disappointed with it and we might even be suffering because of it.

If the answer is suffering – then great, start finding ways out of it, use it to motivate yourself and push yourself towards the solution. Don’t beat yourself up. Nothing good is going to come out of it! Be smart, find a way out of it!

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Confidence and Hard work is the best medicine to kill the disease called failure. It will make you successful person.

Low confidence is a disease, failure is  disease, low aim is a crime!

Gosh there are so many conflicting quotes in this world and sometimes it is really confusing which one to pick. So, for a moment – forget all these quotes.

Although we love quotes at inspire99, I do agree and understand that they tend to get a little romantic and bookish sometimes. Maybe cos these quotes give us only a small picture of life and not the complete story.

I am sure that even these greats had a lot of challenges in life and struggled with their everyday activities. But that’s not their problem – it is our – we tend to idolize every simple person we like.

Instead – start looking at them as human, start looking at failure as a natural phenomenon, quickly find ways to snap out of it and find solutions and look at it as an opportunity or a challenge. There is no point in wallowing in failure, the success is in your attitude of facing these failures.

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Climbing to the top demands strength, whether it is to the top of Mount Everest or to the top of your career.

What is the secret of success? – Talent? Resources? Time? Opportunities?

If someone said persistence/perseverance then I guess you have found the right synonym for strength/success as Kalam points out here.

We all are human and we all have a strong side and a weak side. Sorry to douse the enthusiasm a bit but none of us are perfect, but we sure are beautiful with our imperfections.

The point here is that whatever we would like to do in life – we can’t let the weak side of us call the shots cos it is going to lead us to disaster. We cannot let the fears or past failures guide our futures as well.

We need to focus on our past successes and persist. This strength is going to lead us to the destiny we deserve.

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You cannot change your future, but you can change your habits, and surely your habits will change your future.

What does future hold for us? I feel like a young kid looking at a crystal ball hoping to see my life in a huge mansion with a fleet of cars and riches to command.

Then again – which one of us doesn’t want that? I am not going to debate whether we can change the future or not, but I am going to say that we ought to do everything we can to make that future we desire ours.

I don’t know whether I will be able to change my future or not but I sure would love to do everything in my power to get what I really feel very strongly for. Sometimes it just becomes secondary whether you get to your final destination or not.

And if it simply means changing a few habits, then why not? Are these habits really bigger than our dreams?

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We should not give up and we should not allow the problems defeat us.

 It all boils down to this one simple question – Who is bigger – YOU or YOUR PROBLEMS?

Come on Big Guy, you cannot let every pebble in the way block you. If you hit a pebble it – remove it from your feet, if you hit a wall push through it, jump over it, blast it with dynamite.

Do whatever you think is necessary – but do it. Don’t give in to the idea of failure or self pity. They are not going to lead you anywhere.

It is very easy to gain sympathy or pity in this world. Fortunately RESPECT doesn’t work that way!

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Don’t read success stories, you will only get a message. Read failure stories, you will get some ideas to get success.

It is exciting to read success stories – it fills us with hope, energy and the belief that anything and everything is possible in this world.

And truly enough most of these success stories are tweaked to give you the picture perfect ending we all love to see cos let us face it – tragedies don’t succeed that very well in cinema.

 But that doesn’t mean that we recommend you to read failure stories. NO! We really don’t want you to do that. But we do want you to understand the importance of failures and maybe even appreciate them.

I think what Kalam is trying to say here is that there has never been a respectable success  without a considerable failure. There have been mistakes in the world which have opened up new lines of opportunities and the way we have used them have led us to where we are today.

The best way out is to honor the importance of failures as well, appreciate them and stay clear of them. You don’t have to do all the mistakes to learn from them – you can read a few too 

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Black color is sentimentally bad but, every black board makes the students life bright.

Luck has got nothing to do with your success or life story. I have rarely heard successful people sharing credit with luck.

Luck sure is a very good excuse though, it helps us gratify ourselves and curse the omens. The sad thing about cursing the omens is that they don’t tell you what to do next.

You don’t want someone to tell you or keep telling you that you failed. You already know what you have gone through and defining that is not going to give you much in return.

Instead, look at the next step. Remember – what you see is what you get – you can’t go forward by looking backwards all the time.

Similarly you can’t realize true success if you keep looking at just the failure and just the failure alone.

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Message to Students - Let's make India, a developed nation by our Sincere Efforts, Hardwork & Energy: We all will see our dreams getting true, if we follow path of our "Missileman"

"Our Tribute to real hero of our country"

Dheeraj Awasthi

Manager

CLINI INDIA

089 77 400 800

dheeraj.awasthi@cliniindia.org
http://www.cliniindia.com/