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

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Clinical <b style="box-sizing: border-box;">Trial Management</b></h1>
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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.</div>
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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.</div>
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Work Profile:</h2>
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<li style="box-sizing: border-box; padding: 5px 0px;">Clinical Research Coordinator (CRC)</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Clinical Research Associate</li>
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Clinical Research Coordinator (CRC)</h2>
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The <b style="box-sizing: border-box;">Clinical Research Coordinator (CRC)</b> is responsible for conducting clinical trials using good clinical practice (GCP) under the auspices of the Principal Investigator (PI).</div>
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<li style="box-sizing: border-box; padding: 5px 0px;">All trials are conducted ethically, as defined by the Declaration of Helsinki, rigorously, as defined by the International Conference on Harmonization Guidelines (ICH).</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Benefits outweigh risks for each patient.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Rights, safety and well-being of patients prevail over science.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">All available non-clinical and clinical information on any investigational agent can support the trial as designed.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">All trials are scientifically sound and clearly described.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">All clinical trials have current Institutional Review Board approval.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Medical decisions and care are the responsibility of qualified health care professionals, specifically physicians and, if applicable, dentists.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Everyone involved in the clinical trial is qualified by training, education and experience.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Informed consent is given freely by every participant.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">All study documentation is recorded, handled and stored to allow accurate reporting, interpretation and verification.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Confidentiality of subjects is respected and protected.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Investigational products maintain Good Manufacturing Practice in storage, manufacturing and handling.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Systems to ensure quality are implemented in all aspects of the trial.</li>
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<span style="background-color: white; font-family: Roboto, sans-serif; font-size: 13px; line-height: 18.5714px;">- See more at: http://www.cliniindia.com/clinical-trial-management/#sthash.dFomAIUj.dpuf</span><br />
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Clinical <b style="box-sizing: border-box;">Data Management</b></h1>
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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.</div>
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<b style="box-sizing: border-box;">Work Profile</b></div>
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Clinical Data Analyst/ Manager</h3>
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Job Description</h3>
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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.</div>
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<span style="background-color: white; font-family: Roboto, sans-serif; font-size: 13px; line-height: 18.5714px;">- See more at: http://www.cliniindia.com/clinical-data-management/#sthash.gXOLZ4ls.dpuf</span><br />
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Pharmacovigilance</h1>
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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.</div>
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<b style="box-sizing: border-box;">Work Profile</b></div>
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Drug Safety Associate Responsibilities / Case Processing Expert/ Pharmacovigilance Associate</h3>
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<b style="box-sizing: border-box;">Job Description:</b></div>
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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.</div>
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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.</div>
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<b style="box-sizing: border-box;"> Who hires Pharmacovigilance Professionals?</b></div>
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People trained in Pharmacovigilance can find excellent work opportunities in following organizations:</div>
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<li style="box-sizing: border-box; padding: 5px 0px;">Pharma-Companies ( Novartis, Dr. Reddys, Ranbaxy etc)</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Contract Research Organizations (CROs)</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Biotech companies.</li>
<li style="box-sizing: border-box; padding: 5px 0px;">IT Companies like Accenture, TCS, Cognizant, Wipro, Mahindra Satyam etc</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Regulatory Authorities such as DCG(I), FDA & CDSCO</li>
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<span style="background-color: white; font-family: Roboto, sans-serif; font-size: 13px; line-height: 18.5714px;">- See more at: http://www.cliniindia.com/pharmacovigilance/#sthash.PGxHOPGN.dpuf</span><br />
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Medical Writing</h1>
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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.</div>
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<b style="box-sizing: border-box;">Work Profile</b></div>
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Medical Writer/ Content Writer/ Medical Data Reviewer</h3>
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<b style="box-sizing: border-box;">Job Description</b><br />
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.</div>
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<span style="background-color: white; font-family: Roboto, sans-serif; font-size: 13px; line-height: 18.5714px;">- See more at: http://www.cliniindia.com/medical-writing/#sthash.eLX5CZ3F.dpuf</span><br />
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Regulatory Affairs</h1>
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Pharma regulatory affairs professionals play an essential role in ensuring all pharmaceutical products comply with regulations governing the industry.</div>
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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.</div>
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Regulatory professionals are employed in industry, government and academia and are involved with a wide range of products, including:</div>
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<li style="box-sizing: border-box; padding: 5px 0px;">pharmaceuticals</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Medical devices</li>
<li style="box-sizing: border-box; padding: 5px 0px;">In vitro diagnostics</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Biologics and biotechnology</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Nutritional products</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Cosmetics</li>
<li style="box-sizing: border-box; padding: 5px 0px;">Veterinary products</li>
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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.</div>
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<b style="box-sizing: border-box;">Work Profile</b></div>
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Regulatory Affairs Associate</h3>
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<b style="box-sizing: border-box;">Job Description</b><br />
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.</div>
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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.</div>
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<span style="background-color: white; color: #252525; font-family: Roboto, sans-serif; font-size: 13px; line-height: 18.5714px;">- See more at: http://www.cliniindia.com/regulatory-affairs/#sthash.E4Au9HPu.dpuf</span><br />
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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...

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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">Career Counseling Session on Clinical Research & Pharmacovigilance</span></b><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">Date & Time:</span></b><b><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></b></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"># </span></b><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></b><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: "Trebuchet MS"; mso-hansi-theme-font: major-latin;">CLINI INDIA
      HYDERABAD, Ground Floor, Swathi Plaza, Beside Honda Showroom, Near
      Yashoda Hospital, Rajbhavan Road, So</span></b><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">m</span></b><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: "Trebuchet MS"; mso-hansi-theme-font: major-latin;">a</span></b><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">jiguda, Hyderabad</span></b><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"><br />
      <b><span style="background: yellow;">Date: </span></b></span><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="background: yellow; color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></b><b><span style="background: yellow; color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: "Trebuchet MS"; mso-hansi-theme-font: major-latin;">12 May 2015</span></b><b><span style="background: yellow; color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></b><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">Timing
      - 09:00 am Duration-(2 hours session)</span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">Seats: Only First 30 Candidates allowed for Session<br />
      <span style="background: gold;">Call now @ </span></span></b><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">089 77 400 800 <b><span style="background: gold; color: black;">to block your seat</span></b></span></div>
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<b style="mso-bidi-font-weight: normal;"><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Do you want to know !!!!</span></b></div>
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<b style="mso-bidi-font-weight: normal;"><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Current Job opportunities in Pharma
          Industry?</span></b></div>
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<b style="mso-bidi-font-weight: normal;"><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Pattern of Interview Questions?</span></b></div>
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<b style="mso-bidi-font-weight: normal;"><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Soft skills - Like CV Building,
          Communication etc.</span></b></div>
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<b style="mso-bidi-font-weight: normal;"><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Scope of Clinical Research Industry?</span></b></div>
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<b style="mso-bidi-font-weight: normal;"><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Get Guidance by our Industry Professionals
          to Get Employed..............</span></b></div>
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<span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">Clini India Invites you <b style="mso-bidi-font-weight: normal;">to Join an Introductory Session on Clinical Research,
          Clinical Data Management, Pharmacovigilance and Medical Writing.</b><br />
          This session is going to be highly interactive so as to assist you in
          taking a decision for your career. An opportunity to understand the
          current opportunities in clinical research industry across several
          multinational <b style="mso-bidi-font-weight: normal;">CROs,
          Pharmaceutical Companies and Health Care groups</b>, Session will be
          delivered by senior experts from Industry & will cover all soft
          skills which are required to make bright future.<br />
          <br />
          <b style="mso-bidi-font-weight: normal;">If you are a Fresher or do
          have 0-2 years working experience, this session is Tailor made for
          you.</b></span><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">To book a
          slot for you; Submit your Confirmation here.</span></b><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"> (Fill the form below to Register yourself for
          Session </span><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: "Trebuchet MS"; mso-hansi-theme-font: major-latin;">at our campus</span><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">)<b> 
            </b></span><span style="font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Expert talk
          delivery by :</span></b><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;"></span></div>
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<span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Distinguished
          Professionals from Clinical Research Industry</span><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Option for on
          the spot registration:</span></b><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Candidates
          may enroll during the session by depositing the token amount of 10%
          fee after the workshop, Candidates enrolling the same day will get
          10% flat off in Fees.</span></b></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Promotions
          for courses:</span></b><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;"></span></div>
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<span style="color: black; font-family: Symbol; font-size: 12.0pt; mso-bidi-font-family: Symbol; mso-bidi-font-weight: bold; mso-fareast-font-family: Symbol;"><span style="mso-list: Ignore;">·<span style="font: 7.0pt "Times New Roman";">        
          </span></span></span><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Opt for any mode of training ( Weekdays/ Weekends</span></b><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: "Times New Roman"; mso-hansi-theme-font: major-latin;">)</span></b><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;"></span></b></div>
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<span style="color: black; font-family: Symbol; font-size: 12.0pt; mso-bidi-font-family: Symbol; mso-bidi-font-weight: bold; mso-fareast-font-family: Symbol;"><span style="mso-list: Ignore;">·<span style="font: 7.0pt "Times New Roman";">        
          </span></span></span><b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Blended Learning/ Online.</span></b></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;">Scholarship
          program :</span></b><span style="color: #212223; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-bidi-font-family: Helvetica; mso-hansi-theme-font: major-latin;"></span></div>
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<b><span style="color: black; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;"></span></b><b><span style="background: blue; color: white; font-family: "Cambria","serif"; font-size: 12.0pt; mso-ascii-theme-font: major-latin; mso-hansi-theme-font: major-latin;">Scholarship
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Pharma news - Invitation to attend Free "Counselling Session on Career Opportunities in Clinical Research & Pharmacovigilance" "H1"

Career Counseling Session on Clinical Research &...

Are you looking to join MNC's this June 2015 ? More than 300 vacancies still waiting for you ? Enquire Now !!

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<br />

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<span style="color: red;"><b><span style="background: none repeat scroll 0% 0% white; font-family: "Helvetica","sans-serif"; font-size: 10.5pt; line-height: 115%;">KICK START YOUR CAREER
WITH A LEADER IN CLINICAL RESEARCH</span>!</b></span><span style="color: #141823; font-family: "Helvetica","sans-serif"; font-size: 10.5pt; line-height: 115%;"><span style="color: red;"></span></span></div>
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<span style="background: white;"><span style="-webkit-text-stroke-width: 0px; float: none; orphans: auto; widows: 1; word-spacing: 0px;">For your SUCCESS IN CLINICAL RESEARCH or PHARMACOVIGILANCE
or CLINICAL DATA MANAGEMENT or MEDICAL WRITING or REGULATORY AFFAIRS with PAN
INDIA TRAINING INSTITUTE - CLINI INDIA (HYDERABAD, PUNE, BANGALORE & NAGPUR)</span></span></b></span></span></div>
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<span style="background: white;"><span style="-webkit-text-stroke-width: 0px; float: none; orphans: auto; widows: 1; word-spacing: 0px;">Grab the opportunity now & in 2015 YOU would
be like one amongst the successful 78 candidates who are placed in Pharma
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<span class="textexposedshow">SO WHAT ARE YOU WAITING FOR NOW?</span></span></span></b></span></span></div>
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<span style="font-size: x-small;"><span class="textexposedshow">New weekdays batch announcement – Batch starting
from 5 May 2015 (CLINI INDIA HYDERABAD),</span></span></span></span></b></span></span></div>
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<span class="textexposedshow">To know more about Career, Clinical Research, CDM,
SAS, Oracle, Argus, Pharmacovigilance, Medical Writing jobs details/training or
placements Call now our expert -Tanya @ 07799 844 544 (Office Time) Or Click on
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<br class="Apple-interchange-newline" />CLINI INDIA - Career Counselling Form Join the Best Organization in Placements</h1>
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Are you looking to join MNC's this June 2015 ?<br style="display: block !important;" />More than 300 vacancies still waiting for you ?<br style="display: block !important;" />Enquire Now !!<br style="display: block !important;" />HYDERABAD - BANGALORE  - PUNE - NAGPUR<br style="display: block !important;" />Directly walk in @ CLINI INDIA HYDERABAD Campus at 11:00 a.m. (Monday to Saturday) to meet with Industry Experts or Call @ 089 77 400 800 for Details<br style="display: block !important;" />Address - Clini India, Swathi Plaza, Somajiguda, Hyderabad</div>
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Looking to Join - Advance Program in Clinical Research & Management</div>
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