Courses

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Novel Drug Discovery (Molecular
Modeling & Computer Aided Drug Design)
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Clinical Research, Pharma Research,
Pharmacovigilance & Clinical Data Management - CDM
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SAS, Biostats & Project in Clinical Research
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Features

 Job Oriented Certified Training
  Live Project Experience Certification
 Placement Assistance
 Reco Letters for Abroad
  Guidance for Journal Publications
  Resume Preparation Tips
  SMO Services
BioMed Informatics Clinical Research Homepage

Our Candidates are
Employed with

You Could Become as:
Clinical Research Associate  |  Clinical Research Coordinator  |  Clinical Research Physician  |  Clinical Data Analyst  |  Clinical Data Management Associate  |  Clinical Data Coordinator  |  Clinical Data Monitor  |  R&D Associate  |  Clinical Data Auditor  |  Clinical Pharmacovigilance Associate  |  Regulatory Affairs Associate  |  Clinical Drug Safety Associate  |  SAS Programmer  |  Clinical CRF Designer  |  Healthcare Professional  |  Clinical Data Coder  |  Clinical Data Validator  |  Technical Writer  |  Pharmacist  |  Principal Investigator  |  SOP Writer  |  Health Insurance Associate  |  Medical Record Coordinator  |  New Drug Discovery Scientist  |  Co-Investigator  |  Pharmacovigilance Associate  |  Clinical Reporter  |  Clinical Investigator  |  Regulatory Associate  |  Research Scientist  |  Clinical Pharmacist  |  Safety Processing Expert  |  Scientific Writer  |  Clinical Study Coordinator  |  BioStatistian  |  Clinical SAS Programmer  |  Clinical Statistical Programmer

Potential Employers

 
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WELCOME to BIOMED INFORMATICS BioMed Informatics Medwin Hospitals
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BioMed Informatics Medwin Hospitals was set up as a premier research centre with the objective to offer training solutions in the field of Clinical Research, Pharma Research, Pharmacovigilance, Clinical Data Management (CDM), Statistical Analysis (SAS), Pharmaceuticals, Bioinformatics, In silico Drug Design and Healthcare since the year of 2000.

BioMed Informatics today is one of the best Clinical Research and Clinical Data Management (CDM) training institutes. BioMed Informatics Clinical Research programs enjoy very high level of acceptance from leading global Pharmaceutical, Biotechnology, CROs and Clinical Research companies. BioMed Informatics  Programs are popular amongst the students from India, USA, Mexico, U.K., Canada, Europe, Africa, Asia and Middle East. BioMed Informatics today is the leader in the Clinical Research and Clinical Data Management (CDM) education and training domain.

Good Clinical Practice (GCP) regulations and guidelines govern Clinical Trials, and a thorough knowledge of procedures at every stage of the Clinical Trial process is essential. BioMed Informatics can help you achieve the level of expertise required through our high quality, user-friendly and cost-effective training programs - whether you need to train for a career in Clinical Trials, or update your knowledge with current information.

BioMed Informatics Medwin Hospitals imparting quality Job & Career Oriented Certified Training Programs / Internships in Drug Development Process, Clinical Research, Pharma Research, US FDA Regulatory Affairs, Pharmacovigilance, Clinical Data Management (CDM), Clinical SAS, Bioinformatics, In silico Drug Design with live project implementation and certification.

We also offer Site Management (SMO) Services for Clinical studies to Pharmaceutical, Biotechnology, CRO Companies and Hospitals across a wide range of therapeutic areas.
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News & Events

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We also offer Site Management (SMO) Services for Clinical studies to Pharmaceutical, Biotechnology, CRO companies and Hospitals across a wide range of therapeutic areas. For our SMO services interested organizations can contact us.
 

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