Clinical Research and Pharmacovigilance Courses
GHIS Clinical Research and Pharmacovigilance courses online program is designed to provide total overview and skill globally in the field of clinical research. It would help professionals to upgrade & develop their knowledge about ICH GCP Guidelines, regulatory issues and other major aspects of clinical research & trial management. It is designed to provide total overview and skill globally in the field of clinical research, and pharmacovigilance. It would help professionals to upgrade & develop their knowledge about clinical trials, data management, pharmacovigilance, regulatory issues and other major aspects of pharmacovigilance.
Course Objectives:
The program objective is to understand the key concepts in the responsible conduct of research and that conforms to the highest standards for the protection of human research subjects. It can be able to critically appraise the medical scientific literature, including the methodology of published and proposed investigations. It can be able to independently formulate a research question, as well as be able to design and conduct a study to address that question. It can be able to present and publish the results of one’s scholarly work. It is to identify a focus for future research and scholarly work, and to develop special expertise in the corresponding clinical domain and/or research methods. It would help you to gain in-depth knowledge on the best way to collect and report adverse events and safety data and manage the risk associated with and risk to your products. This advanced training pharmacovigilance short courses in India provide you with the unique format skills and knowledge that needed to operate a fast, effective drug safety or pharmacovigilance program. We provide best diploma, graduate and post graduate certificate courses to college students to enhance their start up in clinical research and pharmacovigilance.
Eligibility: All Science Graduates, MBBS, BDS, BHMS, BAMS, BPT, BUMS, B. Pharm, M. Pharm, Occupational Therapist, B.Sc., M.Sc., Life science, Medical Laboratory, Nursing, Microbiology, Biomedical, Biotech and all professionals working with Hospitals & Healthcare Organizations.
Mode or Methodology: Online & Distance Learning
Examination: Online & Distance Exams (MCQ / Theoretical) / Projects
Placement Assurance: Successful candidates would get the placement support. CVs of successful candidates would be forwarded to various Organizations.
Certification: GIHS Certificate would be awarded to only successful candidates.
Career Options
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Director
To oversee the organisational practice is as per the standard practice and regulatory compliance.
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Associate Director
To guide the team and to ensure that organisation is compliance to the regulatory and organizational standard practice. To meet the client’s requirements and guide the team to achieve the task.
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Project Manger
Responsible for a specific project or several projects within an organization. Oversees the smooth conduct of the clinical study by proper planning and execution.
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Asst. Project Manager
Track work to be done, set desired deadlines and delegate tasks to team, identifying any potential risks.
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Clinical Research Associate
Responsible for setting up, coordinating and supervising clinical studies (trials). Coordinates with executing sites for work. Verify the data collected. Ensures the compliance to regulatory requirements.
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Clinical Trial Assistant
Clinical Research Associate (CRAs) are responsible for coordinating and overseeing the execution of studies and clinical trials by supporting the CRAs and PM.
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Drug safety specialist
Involved in drug safety management. Evaluate and conduct post marketing surveillance of medical drug.
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Pharmacovigilance Associate
Conducts post-market evaluations/surveillance to ensure drug safety. Involved in assessing adverse event writings and maintain the data for safety data and its update.
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Drug Safety Associate
Responsible for assessing the safety of pharmaceuticals drugs after market approval. Assess captured adverse events and case report preparation.
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Senior Clinical Research Coordinator/ Clinical Research Coordinator
Oversees all the tasks at clinical site where trial or studies to be conducted. Include the planning and management of the study, subject enrolment, data maintenance, site staff training initiatives, and maintaining compliance to the regulatory requirements. Work with and under the direction of the clinical Principal Investigator.
Gihsonline Advantage
GIHS provides the best courses helps you to get the start up in the healthcare field. These courses are ad-hoc to your professional career and provide you the additional benefit to be the part of an organization.
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Bringing Excellence To Health Professionals
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10+ Years of Experience
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ISO & GOVT Certified
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Personalized Tutoring for Success
Fees, Payment & Program Duration
Certificate 3 Months- 22000/- INR & Fees for International Candidates – 450$ USD
PG DIploma One Year – 32000/- INR & Fees for International Candidates – 699$ USD
FT PG Diploma 4 Months – 36000/- INR & Fees for International Candidates – 750$ USD
Online Transfer through NEFT or RTGS
Fee can also be deposited in GIHS bank account (For more details Click Here).
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Disclaimer: This course details are for the purpose of awareness about the program and career opportunities.
The exact information on course structure may vary from this information.
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