Courses & Training

Courses & Training

Clinical Research is a branch of Medical Sciences, ‘the study of safety and effectiveness of pharmaceutical products in human subjects in order to disease’s treatment, prevention, diagnosis or for relief’.

Clinical Research in India is one of the fastest growing sectors in the last few years. India being a land of diversity where Ayurveda, Unani, Siddha, and Homeopathy are practiced with the same passion as Allopathy, Clinical studies for evaluation of various alternate systems of medicine can also be conducted with ease.
There is enormous demand for clinical research professionals as India is attracting two-way contract proposals for organize and carry out clinical trials and many entrepreneurs have already move toward the establishment of their Clinical Research Organizations (CRO), and making it as an fascinating career choice with massive growth potential. There is a major gap in Demand & Supply of trained manpower.

Any professionals from Pharmacy, Biotechnology, Practicing Doctors and Graduates from life science can easily find jobs in Clinical Research.

Popular Designations

  • Principle Investigator
  • Investigator
  • Co-Investigator
  • Clinical Research Coordinator(CRC)
  • Clinical Trial Assistant(CTA)
  • Clinical Trial Coordinator (CTC)
  • Patient Care Adviser
  • Site Start-Up Specialist
  • Clinical Research Associate(CRA)
  • Monitor

Clinical research professionals draw highly competitive salaries depending on skills and experience.

“is a process of collecting and validating clinical information with the goal of converting it into an electronic format to answer specific questions and preserve it for further scientific investigations.”

Clinical Research is the source of data for CDM is collected at various stages of the trial. The data which is collected from Clinical sites through paper and electronic documents are entered, stored and protected in database for statistical analysis.

CDM delivers a clean and high quality database for statistical analysis and consequently enables clinical scientists to draw conclusions regarding effectiveness safety and clinical benefit/risk of the drug product under investigations

Popular Designations

  • Clinical data coordinator (CDC)
  • Data Analyst
  • Data Base Programmer
  • Team Lead
  • QA-Associate
  • QA-Lead
  • Project Manager

SAS is highly sophisticated software with well-built data management tools to carry out statistical analysis, data manipulation, and report generation in tables and graphs that precis the data. The heart of the SAS System is Base SAS which is one of the products of SAS. SAS has various tools like BASE SAS, SAS ETL, SAS STAT, SAS SQL, SAS MACRO, SAS REPORTS, SAS GRAPH, SAS BI, SAS VA and many more to carry out various data analysis and reporting.
SAS is a power, flexible, ease of use and has a collection of ready-to-use programs called procedures. The SAS System enables you to perform

  • Data Entry, Data Extraction and Data Transformation.
  • Data Management and Analysis.
  • Data Presentation through various forms like HTML, PDF etc.
  • Applications Development.
  • Forecasting and supporting in Decision making.
  • Quality Improvement

The scope of SAS is exponential for the decade in both India and abroad, even, the beginner’s and entry level programmers can easily able to acquire the skills that are required to translate the data into meaningful information. The following are the sectors where you can find jobs,

  • Automotive
    Education
    Health Insurance
    Insurance
    Media
  • Banking/Financial Services
    Government
    Hospitality & Entertainment
    Life Sciences
    Oil & Gas
  • Communications
    Health Care Providers
    Hotels
    Manufacturing
    Retail & Utilities

Popular Designations

  • SAS Programmer
  • Clinical Data Analyst
  • Statistical Analyst
  • Principal Biostatistician
  • Clinical SAS Programmer/ Analyst
  • SAS Developer
  • SAS Administrator.

Pharmacovigilance (PV) is known as Drug Safety, the Pharmacological Science that is related to Collection, Detection, Assessment, Monitoring, and Prevention of adverse Effects, which occurs from any Pharmaceutical products. The information regarding adverse effects will be received from Patients, Pharmacist and Healthcare providers via Pharmacovigilance agreements (PVAs). In simple, Pharmacovigilance is to identify the harmful effects associated with pharmaceutical products and minimizing the risk of any harm that may come to patients.
A career in PV is exciting with a well defined career path. The growth is fast which eventually leads to official and director roles with good pay packages.

Popular Designations

  • Drug Safety Associate
  • Safety Physician
  • Safety Drug Analyst
  • Safety Writing
  • Medical Information Specialist
  • Medical Officers
  • Medical Liaison
  • Pharmacivigilance Expert

Medical Writing is a vital part of clinical research, it is essential and ever more important activity required at every stage of developing a therapeutic product. Writers works along with the Clinical Data Management, Biostatistics, Pharmacovigilance and Project Management teams to deliver Precise, Well-Timed, credible, complete and Cost effective documents to the main ethical and scientific standards.

Medical Writing is a vital part of clinical research, essential and ever more important activity required at every stage of developing a therapeutic product. Writers works along with the Clinical Data Management, Biostatistics, Pharmacovigilance and Project Management teams to prepare Research-Related documents, Regulatory Documents, Disease Or Drug-Related educational literature, Publication articles and journal in Precise, Well-Timed, credible, complete and Cost effective documents to the main ethical and scientific standards.

To conduct a new clinical studies or for registering new products, many essential documents are required to be submitted to international regulatory agencies such as the US FDA, EMEA, DCGI etc, and these documents will be prepared by medical writers.

Popular Designations

  • Safety Writing Expert (ICSR, PSUR etc.)
  • Medical Writer I (CFR, ICF, Protocol, CRS etc.)
  • Medical Writer II (CFR, IFR, Protocol, CSR etc.)
  • Medical Communication Specialist
  • Proofing ,Editing experts
  • Translator

Medical coding is the transformation of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes.

The diagnoses and procedures are usually taken from a variety of sources within the health care record, such as the transcription of the physician’s notes, laboratory results, radiologic results, and other sources.

Medical coding professionals help ensure the codes are applied correctly during the medical billing process, which includes abstracting the information from documentation, assigning the appropriate codes, and creating a claim to be paid by insurance carriers.

Medical coding is a little bit like translation. Coders take medical reports from doctors, which may include a patient’s condition, the doctor’s diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim.
Healthcare industry is a fast growing industry. The demand for Medical Coders is increasing all over the world day by day.

Medical coding is present a unique set of job duties. It is crucial to understand the way billing and coding works for Fortune 500 health care companies or individuals running their own billing companies out of their home offices.

The physician offices, the hospitals and the insurance companies may demand more and more Medical Coders in future also. Presently the need for coders and billers is high in out sourcing companies in India.

Eligibility

  • BDS
  • Physiotherapy
  • Pharmacy
  • Nursing
  • Any Life Science graduates & Post Graduates
  • IT and Engineering professionals for SAS

 

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