D2L Academy is D2L Pharma’s initiative for bridging up the gap between supply and demand of clinical trial professionals. The courses focus equally on theoretical knowledge as well as practical experience for clinical studies.
The eligibility criteria for admission is as under:
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B.Sc & M.Sc Life Science Graduates
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Graduates in Medicine (M.B.B.S, B.DS, B.H.M.S, M.DS, B.A.M.S, B.PT, M.PT, Nursing)
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Clinical Research Coordinator
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Clinical Research Associates
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Staff nurses or other health professionals who want to become research coordinators
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Research Assistants
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Investigators
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Physicians who want to become Investigators
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Research/Project Managers
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Research Ethics Board Members
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Research Coordinators who want to pursue a career as a Clinical Research Associate
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Bachelor/PhD degrees seeking a career in research
After successful completion of course in our academy, students can enter any of career paths in Clinical Research. On completion of course program the career path of a D2L Academy will provide 100% placement assistance.
Yes, after the classes but during normal office hours.
Training will be held for four hours a day and three days a week.
Our program is totally job oriented and the course curriculum is developed as per the industry requirements. Your future employers are our faculty members. We will provide 100% placement assistance by campus interviews. We are also having in house placement opportunity. During internship, students will be placed directly to the investigator site and in the industry. This will definitely give them a very good opportunity to prove their skills
Yes, we will provide 100% placement assistance to the students.
During internship students will be placed directly in the industry and at the investigator sites so they can have practical approach to Clinical Research Methodology. It is also a good opportunity to prove themselves in the industry.
Job profile of CRC includes
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Management of research study site
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Recruiting, screening and enrolling clinical study participants
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Arranging follow-up visits
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Maintaining and dispensing drug and other study supplies
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Completing and ensuring the accuracy of case report forms and regulatory documents
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Ensuring the adherence to good Clinical Practice guidelines.
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New study site feasibility.
Responsible for monitoring of progress of clinical trial & ensuring that it is conducted according to protocol, standard operating procedure, GCP & the applicable regulatory requirements from starting to end of the study.
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Locating and assessing the suitability of facilities at a study centre.
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Briefing doctors/consultants (or investigators) on conducting the trial.
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Managing regulatory authority applications and approvals.
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Monitoring the trial throughout its duration, this will involve visiting the study centers on a regular basis.
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Verifying that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV).
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Collecting completed CRFs from Research sites.
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Filing and collating trial documentation and reports.
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Ensuring all unused trial supplies are accounted for.
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Close out of the study centers on completion of the trial.
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Discussing results with a medical statistician & other authorities.
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Archiving study documentation and correspondence.
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Preparing final reports.