Advance Diploma and Post Graduate

Regular/Weekend classroom training course offered at SYNCORP's all centers.

Diploma

Course Type

Number of module eligible

Advantages

PG Diploma

3 modules at a time

  • Both theoretical and practical exposure offered.

  • Internship at CRO’s/Trial site

  • Stipend to meritorious candidates

Advance Diploma

2 modules at a time

Diploma

1 module at a time

Training Modules

Clinical Research: Clinical Research is a branch of healthcare that is intended to provide adequate information on use of new drug, new indication of already approved drug, new medical device or new technology with regards to safety, efficacy and adverse effects before introducing it to the market for general public use. Clinical Research in humans is done only after successfully completion and approval of animal studies.

Clinical Research in humans is typically conducted in four phases. Each phase is considered a separate trial and after completion of a phase, Investigators are required to submit their data for approval to the Regulatory body before continuing to the next phase.
Job Profile: Trainee/ Jr.Clinical Research Coordinator, Clinical Research Associate, Clinical Trial Analyst, Associate Clinical Trial Lead, Quality Control Executive, Project lead/ Manager etc.

Who hires:
Pharmaceutical Companies.
Contract Research Organizations (CROs)
Biotech companies.
Knowledge Process Outsourcing (KPOs)
Regulatory Authorities such as DCG (I), FDA & CDSCO
Clinical Trial Sites
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Pharmacovigilance: Pharmacovigilance (PV) is defined as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem. Pharmacovigilance is needed to track unsuspected adverse drug reactions and events. Drug information collected during the pre marketing phase of all medical drugs is inevitable incomplete with regard to possible adverse reactions. Tests done in animals are insufficiently predictive of human safety. In clinical trials patients are selected and limited in number and the conditions of use differ from those in clinical practice and the duration of trails is limited. The information about rare but serious adverse reaction, chronic toxicity, used in special groups such as children elderly and pregnant women or during drug interaction is incomplete or not available.
Job Profile: : Drug safety associate, Drug Safety Scientist, Aggregate report Scientist, Team Lead, Manager etc.

Who hires:
Pharmaceutical Companies.
Contract Research Organizations (CROs)
Biotech companies.
Knowledge Process Outsourcing (KPOs)
Regulatory Authorities such as DCG (I), FDA & CDSCO
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Clinical Data Management: Clinical Data Management (CDM) is the collection, integration and validation of clinical trial data. It is a critical phase in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. This helps to produce a drastic reduction in time from drug development to marketing. Team members of CDM are actively involved in all stages of clinical trial right from inception to completion. During the clinical trial, the Investigators collect data on the patient health for a defined time period. This data is sent to trial sponsor who then analyses the pooled data using statistical analysis
Job Profile: Clinical Data Associate, Associate Clinical data manager, Data Manager, Validation Expert, Subject Matter Expert etc.

Who hires:
Pharmaceutical Companies.
Contract Research Organizations (CROs)
Biotech companies.
Knowledge Process Outsourcing (KPOs)
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Statistical Analysis System (SAS): In a clinical trial lots of data is generated and at the end, this data has to be analyzed and interpreted for the result and then reported to the regulatory body. For this purpose there is a requirement of a tool which can retrieve, analyze, interpret and report the data in accordance to Regulatory requirement. SAS is a tool which provides solution for all these concern in data handling.
Job Profile: : Trainee, Jr SAS Programmer, Sr SAS developer etc.

Who hires:
Pharmaceutical Companies.
Contract Research Organizations (CROs)
Biotech companies.
Knowledge Process Outsourcing (KPOs)
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Regulatory Affairs: Regulatory affairs is a department which has developed from the desire of government to protect public health, by controlling the safety and efficacy of products in areas including Pharmaceuticals, Veterinary medicines, Medical devices, Pesticides, Agrochemicals, Cosmetics and Complementary medicines.
Job Profile: : Regulatory Affairs Associate, Regulatory Scientist, Regulatory affairs specialist etc.

Who hires:
Pharmaceutical Companies.
Contract Research Organizations (CROs)
Biotech companies.
Knowledge Process Outsourcing (KPOs)
Regulatory Authorities such as DCG (I), FDA & CDSCO
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Medical Writing: Medical writing involves communicating often complex data and ideas in a clear, concise, credible, complete, and compelling manner for the better understanding of the general population. Medical writing is an essential and increasingly important activity required at every stage of developing a therapeutic product.
Job Profile: Trainee Scientific Writer, Regulatory Writer, Sr Medical writer, Medico Marketing Writer etc.

Who hires:
Pharmaceutical Companies.
Contract Research Organizations (CROs)
Biotech companies.
Knowledge Process Outsourcing (KPOs)
Regulatory Authorities such as DCG (I), FDA & CDSCO
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Medical Coding: Medical coding is the transformation of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes. Medical coders play a key role in medical process. Medical coding professionals help to ensure that the codes are applied correctly during the medical billing process. These codes are taken from medical transcription, physician’s notes, laboratory and radiologic reports. It is important to document all the treatment or health care service received by the patient every time. The coder will analyze the data from these documents, assign the codes and create the claim to be paid by the patients.

Who hires:
Medical Coding Companies
Biotech companies.
Knowledge Process Outsourcing (KPOs)
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