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~~28000 ₹~~24000 ₹

Advanced

Professional Excellence Program in Pharmacovigilance (PEP-PV)

(5) (4 Reviews)

21:07:01 Hours

40 Lectures

Last updated Tue, 18-Jul-2023

Professional Excellence Program in Pharmacovigilance (PEP-PV)

40 Lessons 21:07:01 Hours English

Our courses have been prepared keeping in mind the current Clinical Research industry requirements so that the deserving candidates can imbibe all the desired concepts of the Clinical Research.

Pharmacovigilance Associate: Responsible for adverse event case processing, data entry, and reporting.
Drug Safety Specialist: Conducts safety assessments, signal detection, and risk management activities.
Pharmacovigilance Scientist: Analyzes safety data, conducts safety signal evaluation, and contributes to safety reports.
Pharmacovigilance Auditor: Performs audits to assess compliance with pharmacovigilance regulations and guidelines.

26000 ₹

Advanced

Professional Excellence Program in Medical Writing(PEP-MW)

(5) (1 Reviews)

13:23:55 Hours

39 Lectures

Last updated Wed, 19-Jul-2023

Professional Excellence Program in Medical Writing(PEP-MW)

39 Lessons 13:23:55 Hours English

Medical writing is the specialized field of creating clear, concise, and accurate content related to medicine and healthcare. It involves translating complex scientific and medical information into accessible language for diverse audiences. Medical writers play a vital role in communicating research findings, clinical trial results, regulatory submissions, and patient education materials. It is a good career choice due to its impact on healthcare, the opportunity to bridge science and communication, and the continuous learning and development it offers. Medical writing provides diverse career options, flexible work arrangements, intellectual stimulation, and the satisfaction of contributing to advancements in healthcare.

Medical Writer: Creates a wide range of scientific and medical documents, including manuscripts, clinical study reports, regulatory submissions, and educational materials.
Regulatory Writer: Specializes in developing regulatory documents for submission to regulatory agencies, ensuring compliance with guidelines and regulations.
Scientific Writer/Editor: Works closely with researchers, scientists, and medical professionals to prepare and edit scientific content for journals, conferences, and other platforms.
Medical Communications Specialist: Engages in medical communications activities, including writing and editing promotional materials, medical education content, and patient materials.

~~24000 ₹~~16500 ₹

Advanced

Professional Excellence Program in Clinical Data Management (PEP-CDM)

(5) (1 Reviews)

18:26:03 Hours

20 Lectures

Last updated Tue, 18-Jul-2023

Professional Excellence Program in Clinical Data Management (PEP-CDM)

20 Lessons 18:26:03 Hours English

Professional Excellence Program in Clinical Data Management

Clinical Data Coordinator: Responsible for data collection, entry, and validation in clinical trials.
Clinical Data Analyst: Analyzes clinical trial data, performs statistical analysis, and contributes to data interpretation and reporting.
Clinical Data Manager: Oversees the entire data management process, including database design, data cleaning, and quality control.

Top 10 Latest courses

~~24000 ₹~~18000 ₹

Intermediate

Advance Program in Clinical Trial Management (AP-CTM)

(5) (4 Reviews)

00:00:00 Hours

10 Lectures

Last updated Wed, 26-Jul-2023

Advance Program in Clinical Trial Management (AP-CTM)

10 Lessons 00:00:00 Hours English

Clinical Trial Management involves overseeing the planning, implementation, and execution of clinical trials to ensure their successful completion. It encompasses activities such as study design, site selection, patient recruitment, data collection, monitoring, and adherence to regulatory guidelines. Clinical Trial Managers play a pivotal role in coordinating various stakeholders, ensuring compliance, and driving the trial towards its objectives. It is a good career choice due to its contribution to advancing medical research, the opportunity to work on cutting-edge treatments, the potential for career growth, and the ability to make a positive impact on patient health outcomes. Clinical Trial Management offers a dynamic and rewarding career path within the pharmaceutical, biotechnology, and clinical research sectors.

Clinical Research Coordinator: Responsible for day-to-day management of clinical trial activities at the site level, including participant recruitment, data collection, and adherence to protocols.
Clinical Research Associate (CRA): Conducts monitoring visits, ensures data quality and regulatory compliance, and maintains effective communication with study sites.
Clinical Trial Manager: Oversees the planning, implementation, and management of clinical trials across multiple sites. They ensure study timelines, budget adherence, and regulatory compliance.
Clinical Project Manager: Manages the overall planning, execution, and coordination of multiple clinical trials, including budget management, team oversight, and study progress tracking.

~~24000 ₹~~16500 ₹

Advanced

Professional Excellence Program in Clinical Data Management (PEP-CDM)

(5) (1 Reviews)

18:26:03 Hours

20 Lectures

Last updated Tue, 18-Jul-2023

Professional Excellence Program in Clinical Data Management (PEP-CDM)

20 Lessons 18:26:03 Hours English

Professional Excellence Program in Clinical Data Management

Clinical Data Coordinator: Responsible for data collection, entry, and validation in clinical trials.
Clinical Data Analyst: Analyzes clinical trial data, performs statistical analysis, and contributes to data interpretation and reporting.
Clinical Data Manager: Oversees the entire data management process, including database design, data cleaning, and quality control.

26000 ₹

Advanced

Professional Excellence Program in Medical Writing(PEP-MW)

(5) (1 Reviews)

13:23:55 Hours

39 Lectures

Last updated Wed, 19-Jul-2023

Professional Excellence Program in Medical Writing(PEP-MW)

39 Lessons 13:23:55 Hours English

Medical Writer: Creates a wide range of scientific and medical documents, including manuscripts, clinical study reports, regulatory submissions, and educational materials.
Regulatory Writer: Specializes in developing regulatory documents for submission to regulatory agencies, ensuring compliance with guidelines and regulations.
Scientific Writer/Editor: Works closely with researchers, scientists, and medical professionals to prepare and edit scientific content for journals, conferences, and other platforms.
Medical Communications Specialist: Engages in medical communications activities, including writing and editing promotional materials, medical education content, and patient materials.

~~28000 ₹~~24000 ₹

Advanced

Professional Excellence Program in Pharmacovigilance (PEP-PV)

(5) (4 Reviews)

21:07:01 Hours

40 Lectures

Last updated Tue, 18-Jul-2023

Professional Excellence Program in Pharmacovigilance (PEP-PV)

40 Lessons 21:07:01 Hours English

Our courses have been prepared keeping in mind the current Clinical Research industry requirements so that the deserving candidates can imbibe all the desired concepts of the Clinical Research.

Pharmacovigilance Associate: Responsible for adverse event case processing, data entry, and reporting.
Drug Safety Specialist: Conducts safety assessments, signal detection, and risk management activities.
Pharmacovigilance Scientist: Analyzes safety data, conducts safety signal evaluation, and contributes to safety reports.
Pharmacovigilance Auditor: Performs audits to assess compliance with pharmacovigilance regulations and guidelines.

Unlock the power of science: embark on a journey in clinical research!

4 Online courses

Expert instruction

Lifetime access

Top categories

Top courses

Professional Excellence Program in Pharmacovigilance (PEP-PV)

Professional Excellence Program in Medical Writing(PEP-MW)

Professional Excellence Program in Clinical Data Management (PEP-CDM)

Top 10 Latest courses

Advance Program in Clinical Trial Management (AP-CTM)

Professional Excellence Program in Clinical Data Management (PEP-CDM)

Professional Excellence Program in Medical Writing(PEP-MW)

Professional Excellence Program in Pharmacovigilance (PEP-PV)

Featured instructor

Admin Cliniversity

Latest blogs

The Importance of Clinical Trial Feedback

AI, big data and clinical trials

The Rise of Home Diagnostics in Clinical Trials

Join now to start learning

Become a new instructor

Unlock the power of science: embark on a journey in clinical research!

4 Online courses

Expert instruction

Lifetime access

Top categories

Top courses

Professional Excellence Program in Pharmacovigilance (PEP-PV)

Professional Excellence Program in Medical Writing(PEP-MW)

Professional Excellence Program in Clinical Data Management (PEP-CDM)

Top 10 Latest courses

Advance Program in Clinical Trial Management (AP-CTM)

Professional Excellence Program in Clinical Data Management (PEP-CDM)

Professional Excellence Program in Medical Writing(PEP-MW)

Professional Excellence Program in Pharmacovigilance (PEP-PV)

Featured instructor

Admin Cliniversity

Latest blogs

The Importance of Clinical Trial Feedback

AI, big data and clinical trials

The Rise of Home Diagnostics in Clinical Trials

Join now to start learning

Become a new instructor

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