ICMR Consultant Recruitment 2023 The Indian Council of Medical Research (ICMR) has released a job notification for the recruitment of 12 Consultant, Project Scientist, and Senior Project Manager Posts. Interested candidates can download the application form from the official website of ICMR. The recruitment drive offers a great opportunity for candidates who are looking to work in the medical research field. The application form is available in PDF format, which can be downloaded and filled out by the candidates. It is important to note that the last date to submit the application form is yet to be announced by ICMR.
ICMR is a premier research organization in India that aims to promote and conduct research in various areas of medical science. The organization is committed to improving the health and well-being of the people of India. The recruitment drive is a great opportunity for individuals who wish to work in the field of medical research and contribute to the development of the healthcare system.
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Notification & Application & Study Materials எடுக்கத் தெரியவில்லை என்றால் இந்த வீடியோ பாருங்க 👉👉👇👇 : https://youtu.be/aIJ8nvm8KLw
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Quick Information About ICMR Consultant Recruitment 2023
| Department Name | ICMR-National Institute of Medical Statistics |
| Category of this Job: | central Government Job |
| Job Type : | Permanent government Jobs |
| Total Vacancies: | Various + post |
| Name Of The Vacancy: | Consultant, Project Scientist, Sr. Project Manager Posts |
| Place Of Postings: | All over India and Tamil Nadu |
| Walk in Date: | 05.04.2023 |
| Apply Mode On: | Offline Mode |
| Official Website Link : | https://main.icmr.nic.in/ |
Disclaimer:
We share private job vacancies that appear daily on our site, accurately and in a way that anyone can understand, and we share full government job details, applications, and job results on our site. Applicants are asked to visit our website daily and select the positions they are applying for.
Vacancy details For this job:
Vacancy Name =Consultant, Project Scientist, Sr. Project Manager Posts
Education criteria :
All candidates must have 10 th to Any Degree for this recruitment.
Full details for this ICMR Consultant Recruitment 2023
Educational Qualifications for Clinical Research and Management Positions
Clinical research is an essential component of medical research, and it requires a team of qualified professionals to conduct successful trials. The qualifications of clinical research professionals may vary based on the job position and the level of experience required for the role. This article focuses on the educational qualifications required for various clinical research and management positions.
- Consultant Scientific (Project Manager) (For TB Vaccine Trial)
The essential qualification for a Consultant Scientific (Project Manager) for TB Vaccine Trial is a professional with a Masters’s degree in life sciences in a relevant subject from a recognized institution with 4-6 years of demonstrated experience in clinical research/clinical trials with published papers. In addition, the desirable qualifications include experience in management and monitoring of clinical research, preparation of SOPs, logs, protocols, and other related documents for trial conduct, CRA experience program, accountable for performance of the studies as per protocol quality standards, and identify and escalate training needs/internal management as needed.
- Project Scientist Support-II (Medical Affairs and Clinical Development) (For ITRC)
The essential qualification for a Project Scientist Support-II (Medical Affairs and Clinical Development) for ITRC is a Post Graduate Degree (MD/MS/DNB) after MBBS with one year experience. Alternatively, a Postgraduate Diploma in Medical subjects after MBBS with two years’ experience or MBBS degree with 4 years experience in clinical research after MBBS. In addition, the desirable qualifications include a Master’s degree in the relevant subject from a recognized university, thorough knowledge of New Drug and Clinical Trial Rules 2019 GCP, ICH guidelines, and regulatory requirements for clinical trial conduct, additional post-doctoral research/teaching experience in relevant subjects in recognized institute(s), knowledge of writing safety reports and SAE, contribute to implementation of clinical protocol and facilitate completion of clinical study reports, and ensure monitoring of safety and adverse events for projects under development.
- Consultant (Clinical Services) (Medical) (For TB Vaccine Trial)
The essential qualification for a Consultant (Clinical Services) (Medical) for TB Vaccine Trial is a Post Graduate Degree (MD/MS/DNB) after MBBS with 2 years experience in clinical research with published papers or Postgraduate Diploma in Medical subjects after MBBS with 4 years’ experience with published papers. In addition, the desirable qualifications include experience in conducting vaccine/drug trial/clinical research/clinical management, able to prepare safety reports and ensure timely management and reporting of AEs and SAEs by sites by supporting them, experience in managing and maintaining databases for quality systems, able to prepare SOPs for trial conduct and write safety reports and SAE narratives, and knowledge of New Drug and Clinical Trial Rules 2019, GCP, ICH guidelines, and other regulatory requirements for clinical trial conduct.
- Consultant (Audit) – For TB vaccine trial
The essential qualification for a Consultant (Audit) for TB vaccine trial is a retired government employee with a Bachelor’s degree in any discipline drawing pay in the Grade Pay of Rs. 5400/- and above at the time of retirement and having at least 10 years’ work experience in the administration, finance, and accounts matters. In addition, the desirable qualifications include proficiency in the latest Accounting packages and Knowledge of MS Office (Word, Power Point, Excel) along with the latest version of Tally.
Title: Project Management and Data Management in Clinical Trials
Introduction:
Clinical trials are essential in the development of new medicines and vaccines. They are highly regulated and require the expertise of qualified professionals to manage and monitor them. This article will focus on two critical roles in clinical trials: Senior Project Manager and Data Management Consultant. The Senior Project Manager is responsible for managing and monitoring regulatory clinical trials, while the Data Management Consultant manages and maintains databases for quality systems. Both roles require specific qualifications and experience, as well as strong communication and problem-solving skills.
Section 1: Senior Project Manager
The Senior Project Manager is a critical role in the development and execution of clinical trials. They lead cross-functional study teams and are responsible for developing and maintaining the Project Management Plan (PMP). They are also responsible for preparing clinical study reports and ensuring that the trial is conducted according to regulatory requirements, such as Good Clinical Practice (GCP), Good Clinical Laboratory Practice (GCLP), and International Conference on Harmonisation (ICH) guidelines.
Qualifications:
The essential qualifications for the Senior Project Manager role include a Master’s degree in Life Sciences with 6-8 years of research experience, including demonstrated core experience in managing and monitoring regulatory clinical trials from reputed institutions. Alternatively, a second-class Master’s degree in Life Sciences with a Ph.D. and 3-5 years of post-Ph.D. experience with demonstrated core experience in managing and monitoring regulatory clinical trials, especially vaccine/drug trials from reputed institutions.
Desirable Qualifications:
The desirable qualifications for the Senior Project Manager role include strong written and verbal communication skills, problem-solving skills, and the ability to monitor project metrics and prepare required updates to ensure the smooth conduct of the trial. The Senior Project Manager should also have a thorough knowledge of new clinical trial guidelines, GCP, GCLP, ICH guidelines, and regulatory requirements for clinical trials.
Responsibilities:
The Senior Project Manager has several responsibilities, including leading cross-functional study teams for the development and execution of clinical trials. They must also develop and maintain the Project Management Plan (PMP), which includes defining the project scope, objectives, timelines, and resources required. The Senior Project Manager is also responsible for preparing clinical study reports, which summarize the trial’s findings and outcomes.
The Senior Project Manager must ensure that the trial is conducted according to regulatory requirements and guidelines, such as Good Clinical Practice (GCP), Good Clinical Laboratory Practice (GCLP), and International Conference on Harmonisation (ICH) guidelines. They must also monitor project metrics and prepare required updates to ensure the smooth conduct of the trial.
Section 2: Consultant (Data Management)
The Data Management Consultant is responsible for managing and maintaining databases for quality systems. They must have expertise in PHP and PHP Frameworks like PDO, Codeigniter, Laravel, and proficiency in scripting languages like jQuery, Ajax, etc. They must also have expertise in MySQL, Postgresql, MS-SQL, Oracle, or equivalent. The Data Management Consultant must have experience in CMS-based web development, including Joomla, Drupal, WordPress, and excellent knowledge of Database Management Systems.
Qualifications:
The essential qualifications for the Data Management Consultant role include a Post Graduate Degree or equivalent in Bioinformatics/Computer Sciences or any related subject from a reputed organization and a Ph.D. in a relevant subject with three years of experience in data management, preferably in clinical research/clinical trials. Alternatively, a Post Graduate Degree or equivalent in Bioinformatics/Computer Sciences or any related subject from a reputed organization with five years of experience in data management, preferably in clinical research/clinical trials.
Clinical research is an essential aspect of the pharmaceutical industry. It involves conducting trials to evaluate the safety and efficacy of new drugs, vaccines, and medical devices. Clinical research coordinators, project scientists, and project coordinators play a vital role in the execution of clinical trials. They ensure that trials are conducted according to Good Clinical Practice guidelines and regulatory requirements. This article will discuss the essential and desirable qualifications for various positions in clinical research, including Clinical Research Coordinator, Project Scientist Support-V (Clinical Operations), Consultant Scientific (Project Coordinator) (For Tribal TB Project), Consultant Scientific (Medical) (Project Coordinator) (For Mission Mode Saharia TB project), and Consultant Scientific (Non-Medical) (Project Coordinator) (For Mission Mode Saharia TB project).
Clinical Research Coordinator
Clinical research coordinators are responsible for the coordination and management of clinical trials. They ensure that trials are conducted ethically and in compliance with regulatory requirements. To become a clinical research coordinator, a candidate must have a Bachelor’s Degree in Bio-sciences, Biotechnology, Life Sciences, or any equivalent field with three years of relevant experience. Alternatively, a postgraduate degree in any of these fields is also acceptable. Additionally, experience in handling databases and computer applications and conducting vaccine/drug trials or clinical research is desirable. The ability to prepare safety listings, tables, SOPs, and logs is also crucial, along with thorough knowledge of new drug and clinical trial rules, GCP, ICH guidelines, and regulatory requirements.
Project Scientist Support-V (Clinical Operations)
Project Scientist Support-V (Clinical Operations) is responsible for the monitoring of clinical trials and ensuring their timely completion. They are also responsible for monitoring project data, eCRF data entry, and query resolution. A first-class Master’s degree in Biotechnology, Clinical Pharmacology, Life Sciences, or any equivalent degree with four years of experience in CRO industry, Pharma, Biotech, Public Health, or clinical research is the essential qualification for this position. Alternatively, a second-class M.Sc. or M.Pharm or any equivalent degree with a Ph.D. degree in Biotechnology, Pharmacology, or Life Sciences with two years of experience in Pharma, Biotech, CRO industry, Public Health, or clinical research is also acceptable. Additionally, experience in protocol writing, monitoring site performance, and providing guidance to study sites, along with preparing quality trending reports, is desirable.
Consultant Scientific (Project Coordinator) (For Tribal TB Project)
Consultant Scientific (Project Coordinator) is responsible for planning and executing field studies for the Tribal TB Project. The essential qualification for this position is a Ph.D. in Anthropology or Social Science from a recognized institution with 12-15 years of relevant experience in community work, clinical research, or qualitative research. Experience in qualitative software, leading cross-functional study teams, and developing project management plans and community engagement plans is desirable.
Consultant Scientific (Medical) (Project Coordinator) (For Mission Mode Saharia TB project)
Consultant Scientific (Medical) (Project Coordinator) is responsible for planning and executing community studies, field interventions, and public health studies for the Mission Mode Saharia TB project. The essential qualification for this position is an M.D./D.N.B. or Ph.D. after MBBS from a recognized institution with a good publication record and 3-5 years of relevant experience in community work, community public health, and clinical research. Additionally, experience in managing public health, patient management in the field, conducting telemedicine, and coordinating with experts in relevant areas is desirable. Knowledge of computer applications, data management, report writing, data mining, and working on databases is also required.
Title: Consultant Scientific (Non-Medical) – A Key Player in the Saharia TB Project
The Saharia TB project is a mission mode project aimed at controlling and preventing the spread of tuberculosis in the Saharia tribal region of India. This project requires the expertise of a Consultant Scientific (Non-Medical) with a Ph.D. in Public Health/Life Sciences from a recognized institution and a good publication record. The ideal candidate must possess a minimum of 8-10 years of relevant experience in clinical and field studies.
In addition, the candidate should have experience in conducting, planning, and executing community studies, field intervention studies, especially in the area of TB. The ability to independently execute and handle field research projects and lead cross-functional study teams for the execution of multicentric field studies is also essential. The consultant scientific must also have experience in managing and maintaining the database of research projects in the area of TB.
The successful candidate must be able to develop and maintain the Project Management Plan (PMP) and develop a community engagement plan. A thorough understanding of computer applications, report writing, data management, data mining, and working on databases is also essential.
Clinical Studies
Tuberculosis (TB) is a contagious disease caused by the bacterium Mycobacterium tuberculosis. It affects the lungs primarily but can also affect other parts of the body such as the kidneys, spine, and brain. TB is spread through the air when an infected person coughs or sneezes. It is a preventable and curable disease, but it remains a significant global health problem. India has the highest burden of TB in the world, with an estimated 2.8 million new cases and 435,000 TB-related deaths in 2019. The Saharia TB project aims to address this issue by developing interventions and strategies to control and prevent the spread of TB in the Saharia tribal region of India.
Clinical studies are an essential component of the Saharia TB project. The consultant scientific will be responsible for planning, executing, and managing clinical studies in the Saharia tribal region. Clinical studies involve testing new drugs, vaccines, or medical devices on human subjects to determine their safety and efficacy. The consultant scientific will work with the study team to develop study protocols and obtain ethical clearance from the appropriate regulatory bodies. They will also be responsible for monitoring the progress of the study, collecting and analyzing data, and reporting the results.
Field Studies
Field studies are another crucial component of the Saharia TB project. Field studies involve conducting research in real-world settings such as communities, schools, or workplaces. The consultant scientific will be responsible for planning, executing, and managing field studies in the Saharia tribal region. They will work with the study team to develop study protocols, obtain ethical clearance, and recruit study participants. The consultant scientific will also be responsible for monitoring the progress of the study, collecting and analyzing data, and reporting the results.
Data Management
Data management is an essential aspect of any research project. The consultant scientific will be responsible for managing and maintaining the database of research projects in the area of TB. They will work with the study team to develop data collection tools, ensure data quality, and perform data cleaning and analysis. The consultant scientific will also be responsible for preparing data for publication and sharing data with other researchers and stakeholders.
Project Management
The consultant scientific will play a crucial role in the project management of the Saharia TB project. They will develop and maintain the Project Management Plan (PMP) and develop a community engagement plan. The PMP is a document that outlines the scope, objectives, deliverables, timelines, and resources required for the project. The community engagement plan is a strategy for involving the community in the project and ensuring their participation and support. The consultant scientific will work with the study team
Important Dates For This Job:
| Walk in Date: | 05.04.2023 |
Official Notification & Application ICMR Consultant Recruitment 2023
| ICMR Consultant Recruitment 2023 Official Website Link | CLICK HERE |
| ICMR Consultant Recruitment 2023 Official Notification Link | CLICK HERE |
| ICMR Consultant Recruitment 2023 Official Apply Link | CLICK HERE |
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Notification & Application & Study Materials எடுக்கத் தெரியவில்லை என்றால் இந்த வீடியோ பாருங்க 👉👉👇👇 : https://youtu.be/aIJ8nvm8KLw
👇 HERE YOU CAN JOIN OUR SAI VIKRAM ACADEMY FAMILY👇
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