Research & Program

WHY REZANTECH TECHNOLOGIES ?

Market Leaders In Innovation

We are clearly the market leaders in terms of our self designed, up-to-date industry-integrated curriculum, as well as the technical and soft skills we impart to our students, while making them adept at the use of modern technology.

Best Placement Record In the Industry

Our commitment to our students does not just end with providing them the best skills and training possible, but also to helping them start their career with the best names in the industry. No wonder, we have the best placement record for Clinical Research professionals and our previous batch students are placed with top CROs, Pharmaceuticals and Bio-tech companies.

 

The Rezantech Technologies Culture of Growth

At REZANTECH TECHNOLOGIES, one of the top clinical research institutes , we have established a culture of constant growth, innovation and enterprise in a professional environment aided with state-of-the-art facilities, led by our supportive staff who teach professionally every aspect of online/ Direct clinical research & pharmacovigilance courses

  • ADVANCE PG DIPLOMA IN CLINICAL RESEARCH  PHARMACOVIGILANCE 
  • PG DIPLOMA IN CLINICAL RESEARCH & PHARMACOVIGILANCE 
  • DIPLOMA IN CR & PV 
  • CERTIFICATION IN CR & PV

rezantech technologies

Adv. PG Diploma in Clinical Research & Pharmacovigilance

Pharmacovigilance is regarded as an evergreen industry. It is at the center stage of new drug development as well as post marketing evaluation of approved drugs and devices. Pharmacovigilance is a scientific discipline which is mainly concerned with identifying, validating, quantifying, evaluating and increasing their safety. The main activities in a pharmacovigilance involve providing end to end medical, safety and analytical services which include medical review, expectedness, casualty assessment, case narratives and processing, coding using medical dictionaries (e.g, MedDRA), data mining and signal detection, medication error related activities and finally some specialized regulatory services

The basic minimum qualifications for fitting to a pharmacovigilance career include undergraduate and/or graduate degrees in human (MBBS, BDS) and veterinary (BVSC) medicine, BAMS, BUMS, pharmacy (B.Pharm), nursing (BS) or allied health sciences (BSc); after which a course in Post Graduate Diploma in Clinical Research & Pharmacovigilance can be applied for.

The professional clinical research & pharmacovigilance diploma courses in pharmacovigilance will provide a foundation in pharmacovigilance principles and operations. The curriculum is fully reviewed by the industry professional and is relevant to aspirants who want to join the pharmacovigilance sector from both within and outside the pharmaceutical industry

PG Diploma in Clinical Research & Pharmacovigilance

The PG Diploma Clinical Research programme will help the life science and health science graduates to learn about the life cycle of a drug and provide an understanding on the process involved in the movement of a drug from the bench side to the bedside. It will also give an insight into clinical trial approval processes, marketing approval processes and about the different regulatory authorities pertaining to product registration across the globe.

Is this program right for me?

If you are passionate about working with clinical data and looking forward to working in Site Management Organisations (SMOs), Contract Research Organisations (CROs), Pharmaceutical Companies and MNCs PG Diploma Clinical Research course is the right choice.

Who can apply?

MBBS/BHMS/BAMS/BPT/MPT/BDS/BMLT/ Bachelor in Naturopathy & Veterinary Science /MD/MS. Graduate/Postgraduate degree in Pharmacy/ Pharmaceutical Sciences. Graduate/Postgraduate degree in Life Sciences (Botany, Zoology, Biochemistry, Microbiology, Genetics, Biotechnology). Graduate/Postgraduate degree in Chemistry/Biostatistics/ Bioinformatics. Graduate or equivalent degree in Nursing/Allied Health. Students in their final year of graduation for the above courses may also apply.

What are the job opportunities for clinical research?

The PG Diploma Clinical Research programme will give an opportunity to work in Multinational Companies. 

 

Students can get engaged in different profiles like 

 

ü  Clinical Trial Analyst 

ü  Clinical Trial Assistant 

ü  Clinical Research Co-Ordinator 

ü  Clinical Research Associate 

ü  Quality Control 

ü  Quality Analyst 

ü  Principal Investigator 

ü  Sub-Investigator

What are the job opportunities for Clinical Data Management?

ü  Data Entry Operator 

ü  Associate Clinical Data Co-Ordinator 

ü  Data Validator 

ü  Medical Coder 

ü  Data Manager 

ü  Clinical Data Analyst 

ü  Clinical Data Programmer 

ü  Clinical Data Manager I 

ü  Clinical Data Manager II 

ü  Principal Clinical Data Manager 

ü  Manager, Clinical Data Management 

ü  Group Manager, Clinical Data Management 

ü  Associate Director, Clinical Data Management

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Clinical Research Associate (CRA)

(CRA) is a health-care professional who performs activities related to clinical trials. They are the soul in the field of Clinical Research. The experts find their place in various organizations such as pharmaceutical companies, medical research institutes and government agencies. Depending on the organization’s policies different education and certification requirements may be necessary to practice as a Clinical Research Associate.

Clinical Data Management (CDM)

(CDM) is a critical phase in clinical research. CDM leads to generation of superior quality, dependable, and statistically well informed data from clinical trials. The ultimate goal of CDM is to assure a well maintained data support conclusions drawn from research and thus achieving this goal protects public health and creates confidence in the world of therapeutics.

Clinical Research Organisation (CRO)

(CRO) A CRO landscape is vast; using a CRO’s expertise you can maximize the efficiency of your clinical trials, but only if you choose the right one for the project at hand. Typically, a CRO will organize and conduct clinical trials to check the test molecule in humans. As independent companies, they offer an objective assessment of a new drug in the clinical setting and since they partner with many companies, typically provide broader experience.

Careers In Clinical Research

Key Cities in India for Clinical Research

  • Delhi & NCR Region 

  • Mumbai 

  • Pune 

  • Ahmedabad

  • Vadodara

  • Hyderabad 

  • Bangalore 

  • Chennai

  • Chandigarh

  • Bhopal, Indore, Coimbatore & Vizag are emerging as new centres for clinical trials

Career options after BVMS / BSMS / BAMS / BPT / MBBS/ BDS

Clinical research refers to the process, which is basically the evaluation of how effective or useful a new drug, vaccine, diagnostic test, new device or surgical technique, can be in humans.

Careers In Clinical Research

Advantages of doing a CR course

The number of trials approved by the Drugs Controller General of India is on the rise, with India becoming a one-stop destination for many disease indications, and both MNC and Indian companies eager to conduct multinational multi-centric trials here.

CROs, as the name suggests, offer a wide range of “outsourced” pharmaceutical research services to pharmaceutical industries and hence are the next big employers of clinical research professionals.

India is the second largest pharmaceutical market in Asia growing by more than nine per cent annually. According to a report, there are more than 50,000 jobs in clinical research in India.

Various job roles available

  • Principal Investigator 

  • Co-investigator 

  • Medical Advisor 

  • Drug Developer 

  • Clinical Research Physician 

  • Technical writer 

  • Protocol Development 

  • Pharmacovigilance dept. in pharma companies 

  • Regulatory Affairs Manager

  • Clinical Research Physician