#Pharmacovigilance training in mumbai

[sudheervanguri]

Junior Data Analyst (CDM/PV) Recruitment Cognizant, a leading global provider of professional services, is seeking talented individuals for the position of Junior Data Analyst (CDM/PV) in Mumbai. This full-time role offers an exciting opportunity for graduates and postgraduates in life sciences, pharmacy, or medical sciences to join a dynamic team and contribute to clinical data management and pharmacovigilance processes. Key job details Job number: 00060240971 Travel required: No Job category: Technology & Engineering Employment type: Full-time Job Responsibilities As a Junior Data Analyst in the CDM/PV domain, your responsibilities will include: Responsibility: Manage and process pharmacovigilance cases to ensure compliance with regulatory requirements. Oversee the accurate and timely entry of data into the PV database. Provide support in the preparation of safety reports and regulatory submissions. Collaborate with cross-functional teams to ensure the accuracy and completeness of case information. Utilize MS Excel to analyze and report on PV data. Ensure adherence to standard operating procedures and guidelines. Conduct quality checks on case processing activities to maintain high standards. Assist in the development and implementation of process improvements. Participate in training sessions to stay updated on regulatory changes and industry best practices. Contribute to research and development initiatives by providing PV insights. Support the team in handling complex cases and resolving issues. Maintain up-to-date knowledge of pharmacovigilance regulations and guidelines. Communicate effectively with stakeholders to ensure clarity and accuracy in PV processes. Qualifications Possess a strong understanding of PV case processing and regulatory requirements. Demonstrate proficiency in MS Excel for data analysis and reporting. Have experience in research and development which is a plus. Exhibit excellent attention to detail and accuracy in data entry and case processing. Show strong organizational and time management skills. Display effective communication and collaboration abilities. Maintain a proactive approach to problem-solving and process improvement. Stay updated with industry trends and regulatory changes. Demonstrate the ability to work independently and as part of a team. Have a commitment to maintaining high-quality standards in all tasks. Show a willingness to participate in ongoing training and development. Possess a minimum of 2 to 3 years of relevant experience in PV case processing. Hold a relevant degree in life sciences or a Certifications Required CERTIFIED PHARMACOVIGILANCE PROFESSIONAL (CPP) OR EQUIVALENT CERTIFICATION IN PHARMACOVIGILANCE. How to Apply Apply online through the following link: Cognizant Careers.

[pharmamentorsedu]

Where Can I Learn Pharmacovigilance and Clinical Research in Mumbai, India?

If you're seeking to pursue a Pharmacovigilance course in Mumbai, India, there are several options available to you. One notable choice is Pharmamentors, a leading institute offering specialized training in pharmacovigilance.

Located in Mumbai, Pharmamentors provides comprehensive courses tailored to meet the demands of the pharmaceutical industry. Their curriculum covers essential topics such as drug safety regulations, adverse event reporting, risk management, and pharmacovigilance methodologies.

With experienced faculty members and interactive learning modules, Pharmamentors ensures that students gain practical skills and knowledge essential for a career in pharmacovigilance. Additionally, the institute may offer placement assistance, helping students transition smoothly into the workforce.

By choosing Pharmamentors in Mumbai, aspiring pharmacovigilance professionals can access quality education and enhance their prospects in the pharmaceutical field.

#pharmacovigilancecourse

[techdata1]

Clinical Research Course Pune & Mumbai

Top Clinical Research Course

Since the technological revolution, the world has emerged as a superpower with a major breakthrough in the field of healthcare and science which has increased the inquisitiveness to research and discover new findings. The amalgamation of IT, pharmaceutical, and biotech research is one such multi-disciplinary field which has given birth to infinite innovations and has been growing incessantly over the past decades. These innovations have paved paths for innumerable opportunities in the world of medicines and clinical research which have led to the constant rise in demands for jobs in clinical research fields.

Before we dig deeper into the various segments of the clinical research course, let us decode the conundrum of clinical research and how one can benefit from this course, professionally.

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Clinical Research

Clinical research, yet another vertical of healthcare that focuses on trials with new drugs on patients and humans at the initial level to discover the cure for the deadly diseases. The study determines the safety, accuracy, and effectiveness of medicines and clinical devices which are tested before they are approved by the government or other regulating bodies. Clinical experts and professionals then utilize the new drugs produced to improve the health of the patients with certain sets of standards and protocols.

With the data outgrowing the population, the constant demand for clinical research and clinical data management is always on a rise. Being one of the richest designations in the world, clinical research certifications and jobs are not just worth the pay but also are liable for global recognition. This is why there is a global demand for the trained and certified clinical research professionals in the healthcare and research industry.

Best Clinical Research Course in Pune and Mumbai

Clinical Research course in Pune is curated by an adroit team of clinical research training experts who possess years of experience and expertise in the field of innovation and clinical research. TechData Solutions, one of the top clinical research course providers in Pune and Mumbai offer an exclusive platform for beginners, professionals, and students to upscale their career and widen their knowledge in the areas of clinical research. The clinical research course in Mumbai too offers an extensive training scope that includes Clinical Research Training (CTM), Pharmacovigilance(PV) training, Clinical Data Management (CDM), and Regulatory affairs.

Clinical Research Course Modules

TechData Solutions offers the best clinical research course in Pune with both technical knowledge and practical case studies. The instructor-led clinical research course in Mumbai covers the primary modules of clinical research - CDM, PV, and Regulatory Affairs with 24*7 guidance and support that fits the real-time industrial requirements. Let us walk you through the modules of clinical research and the course curriculum.

[resoveitech]

Introducing medical coding training and learn how to get started.

What is medical coding? It reviews the patient's medical record and converts it into standard medical codes that are easily understood by third parties, such as insurance companies or health care facilities. Medical training is essential for those planning to become medical programmers. Since this job requires one to be a professional, one has to study and practice medical coding. Although there are still requirements for certification, the medical programmer must continue to be trained to deal with accuracy and accuracy at work. Therefore, it is highly recommended that one learns work-related theories. In general, the training includes taking programs to study theories in standard medical symbols, medical terminology, pharmacy, anatomy, disease, insurance, and medical care. There is currently little focus on hands-on training in real hospitals and clinics. However, there is still a growth in the need for medical coding and we may see more changes in available training programs in the future.

There are many resources for a degree in Medical coding Institute. There is medical coding training offered by various universities and colleges across the country. Online courses and classes are also available. One can choose to study full or part-time, either in the classroom or online. Online training is more convenient and flexible for a person who may have a current job and chooses to take it as a part-time study. An investigation is recommended to obtain more details about the resources available to determine where and how to obtain this certification.

Obviously, the one receiving Medical coding training in Mumbai will end up working as a medical programmer. Most medical programmers usually work in hospitals or clinics. Somehow, there is an increasing trend for this profession to be home-based, although it is quite unlikely at the moment.

[clininfotechseo]

Get to know about best Pharmacovigilance Training institutes in Pune

Nowadays due to the competition in the educational field people are urged of opening institutes without having any proper infrastructure or faculty. If you are searching for the best training institute in Pune for clinical training then Clin Infotech is the landing place for you. Here you will get practical and theoretical knowledge in any course. We are offering you e-learning access to our students, 2 sets of mock examinations, knowledge area-wise mock tests, 35 contact hours. The instructor is providing free training online. Want to enroll in Pharmacovigilance Training institutes in Pune then visit our website at www. Clininfotech.com.

[cliniindia]

Clini India, one of the top Clinical Research institutes in Bangalore, Hyderabad, Pune and Mumbai, Our Institute offers courses in Clinical Research, Clinical Data Management, Pharmacovigilance, Medical Writing and Clinical SAS. We are SAS Accredited and ISO Certified Clinical Research Institute. Learn From online or offline, Flexible Classes, training with placement Assistance.

[drvijendrakumarjain]

Best Neurosurgeon In Delhi | Neurologist in Delhi - Dr. VK JAIN

Dr. V K Jain is the Principal Director of Neurosurgery and Spine Surgery at Max Hospitals in Delhi and NCR.

Dr. Vijendra Kumar Jain is one of the best neurosurgeons and spine surgeons in India. He is the head of Max Hospitals' Neuro and Spine Department in Delhi and NCR region. He has over 41 years of experience in Neurosurgery. He is the most recommended neurosurgeon in India by patients. He has performed over 16,000 procedures and is recognized for his expertise and skill in the field.

He is known for his surgical precision and his expertise lies in treating tumors, aneurysms, spinal cord injuries, and other conditions related to brain and spine. Patients from all over the world travel to India to seek his expertise in neurosurgery. Dr. Jain's passion for clinical work and his training as well as research allow him to be a standout neurosurgeon in India. He has penned a substantial number of papers in peer-reviewed journals and has been a keynote speaker at several medical conferences. His research and innovative surgical techniques have earned him well-deserved repute in the medical field.

Qualification

Dr. Jain completed his MBBS from King George's Medical College, Lucknow, in 1974. He completed his MCh in Neurosurgery from the esteemed National Institute of Mental Health and Neurosciences (NIMHANS) Bangalore. He did a Fellowship in Micro-neurosurgery at the Fujita Health University, Nagoya, Japan.

Fellowships & Memberships

Dr. V K Jain is a member of various associations and scientific societies like:

Neurological Society of India

Epilepsy Society of India

Indian Society of Cerebrovascular Surgery

Indian Society of Paediatric Neurosurgery

Neurotrauma Society of India

Skull Base Surgery Society of India

Society of Pharmacovigilance (India)

Asian Congress of Neurological Surgery

Asian Australasian society of Neurological Surgeons.

Dr. V K Jain has been serving as an Editorial Board Member of the Journal of Postgraduate Medicine, Mumbai, Neurology India, the Official Journal of Neurological Society of India, Indian Journal of Neurotrauma, Spine, Surgical Neurology International.

He has also been appointed as a keynote speaker for numerous events around the world. He has been invited to function as a professor at numerous conventions, venues, and seminars both in India and abroad.

Work Experience

41 years of experience in Neurosurgery

Currently, Principal Director at Department of Neurosurgery at Max Hospitals in Delhi and NCR region

Chairman of the Neurosurgery Department, Sir Ganga Ram Hospital, since February 2010

Prof. at SGPGIMS, Lucknow, from Apr 1999 to Feb 2010

Visiting Professor at University Hospital of Geneva, Geneva, Switzerland from 15th to 30th June 2001

Visiting Professor at Fujita Gakuen Health University, Toyoake, Aichi, Japan from 03.05.1999 to 29.05.1999

Additional Prof. at SGPGIMS, Lucknow, September 1987 to April 1999

Associate Prof. at NIMHANS, Bangalore, December 1984 to September 1987

Assistant Prof. at NIMHANS, Bangalore, September 1981 to December 1984

Dr. Jain has numerous publications to his name.

Research Papers & Publications

His book - “Craniovertebral Junction Anomalies – The Indian Experience“, was published in 1997 and is still a useful guide to the medical industry.

In 2018, he co-edited a book on “Craniovertebral Junction Disorders”.

His opinions have also been featured in books on various aspects of Neurosurgery.

His articles regarding Neurology and Neurosurgery have been featured in many publications such as Surgical Neurology, Journal of Neurosurgery, Neurosurgery, Neurology India, Indian Journal of Neurotrauma etc.

Dr. Jain is a highly respected and highly esteemed figure in the medical world due to his contributions in teaching and research. He is highly respected and loved by his patients as he is very patient and family oriented for his patients and always there for them despite his busy schedule.

TAG- Best Neurosurgeon in delhi, Neurologist in Delhi, Brain Tumor Surgery in Delhi, Dr. Vk Jain

[spinespecialistinindia]

Best Neurosurgeon and Spine Surgeon in India

Dr. Vijendra Kumar Jain

MBBS, MCh - Neuro Surgery

Neurosurgeon, Spine Surgeon, 41+ Years Experience

Dr. V K Jain is the Principal Director of Neurosurgery and Spine Surgery at Max Hospitals in Delhi and NCR.

Dr. Vijendra Kumar Jain is one of the best neurosurgeons and spine surgeons in India. He is the head of Max Hospitals' Neuro and Spine Department in Delhi and NCR region. He has over 41 years of experience in Neurosurgery. He is the most recommended neurosurgeon in India by patients. He has performed over 16,000 procedures and is recognized for his expertise and skill in the field.

He is known for his surgical precision and his expertise lies in treating tumors, aneurysms, spinal cord injuries, and other conditions related to brain and spine. Patients from all over the world travel to India to seek his expertise in neurosurgery. Dr. Jain's passion for clinical work and his training as well as research allow him to be a standout neurosurgeon in India. He has penned a substantial number of papers in peer-reviewed journals and has been a keynote speaker at several medical conferences. His research and innovative surgical techniques have earned him well-deserved repute in the medical field.

Qualification

Dr. Jain completed his MBBS from King George's Medical College, Lucknow, in 1974. He completed his MCh in Neurosurgery from the esteemed National Institute of Mental Health and Neurosciences (NIMHANS) Bangalore. He did a Fellowship in Micro-neurosurgery at the Fujita Health University, Nagoya, Japan.

Fellowships & Memberships

Dr. V K Jain is a member of various associations and scientific societies like:

Neurological Society of India

Epilepsy Society of India

Indian Society of Cerebrovascular Surgery

Indian Society of Paediatric Neurosurgery

Neurotrauma Society of India

Skull Base Surgery Society of India

Society of Pharmacovigilance (India)

Asian Congress of Neurological Surgery

Asian Australasian society of Neurological Surgeons.

Dr. V K Jain has been serving as an Editorial Board Member of the Journal of Postgraduate Medicine, Mumbai, Neurology India, the Official Journal of Neurological Society of India, Indian Journal of Neurotrauma, Spine, Surgical Neurology International.

Work Experience

41 years of experience in Neurosurgery

Currently, Principal Director at Department of Neurosurgery at Max Hospitals in Delhi and NCR region

Chairman of the Neurosurgery Department, Sir Ganga Ram Hospital, since February 2010

Prof. at SGPGIMS, Lucknow, from Apr 1999 to Feb 2010

Visiting Professor at University Hospital of Geneva, Geneva, Switzerland from 15th to 30th June 2001

Visiting Professor at Fujita Gakuen Health University, Toyoake, Aichi, Japan from 03.05.1999 to 29.05.1999

Additional Prof. at SGPGIMS, Lucknow, September 1987 to April 1999

Associate Prof. at NIMHANS, Bangalore, December 1984 to September 1987

Assistant Prof. at NIMHANS, Bangalore, September 1981 to December 1984

Dr. Jain has numerous publications to his name.

Research Papers & Publications

His book - “Craniovertebral Junction Anomalies – The Indian Experience“, was published in 1997 and is still a useful guide to the medical industry.

In 2018, he co-edited a book on “Craniovertebral Junction Disorders”.

His opinions have also been featured in books on various aspects of Neurosurgery.

His articles regarding Neurology and Neurosurgery have been featured in many publications such as Surgical Neurology, Journal of Neurosurgery, Neurosurgery, Neurology India, Indian Journal of Neurotrauma etc.

Dr. Jain is a highly respected and highly esteemed figure in the medical world due to his contributions in teaching and research. He is highly respected and loved by his patients as he is very patient and family oriented for his patients and always there for them despite his busy schedule.

If you have any sort of neuro and spinal issues, do not hesitate to schedule an appointment with Dr. VK Jain.

TAG : Best Spine Surgeon in India, Spine Specialist in India, Neurologist in India, Best Brain Tumor Surgeon in India, Best Neuro Surgeon in India, Neurosurgeon in India, Spine Surgeon in India

[drvijenderkumarjain]

Best Neurosurgeon and Spine Surgeon in India-Dr. Vk Jain

Dr. V K Jain is the Principal Director of Neurosurgery and Spine Surgery at Max Hospitals in Delhi and NCR.

Dr. Vijender Kumar Jain is one of the best neurosurgeons and spine surgeons in India. He is the head of Max Hospitals’ Neuro and Spine Department in Delhi and NCR region. He has over 41 years of experience in Neurosurgery. He is the most recommended neurosurgeon in India by patients. He has performed over 16,000 procedures and is recognized for his expertise and skill in the field.

He is known for his surgical precision and his expertise lies in treating tumors, aneurysms, spinal cord injuries, and other conditions related to brain and spine. Patients from all over the world travel to India to seek his expertise in neurosurgery. Dr. Jain’s passion for clinical work and his training as well as research allow him to be a standout neurosurgeon in India. He has penned a substantial number of papers in peer-reviewed journals and has been a keynote speaker at several medical conferences. His research and innovative surgical techniques have earned him well-deserved repute in the medical field.

Qualification

Dr. Jain completed his MBBS from King George’s Medical College, Lucknow, in 1974. He completed his MCh in Neurosurgery from the esteemed National Institute of Mental Health and Neurosciences (NIMHANS) Bangalore. He did a Fellowship in Micro-neurosurgery at the Fujita Health University, Nagoya, Japan.

Fellowships & Memberships

Dr. V K Jain is a member of various associations and scientific societies like:

Neurological Society of India

Epilepsy Society of India

Indian Society of Cerebrovascular Surgery

Indian Society of Paediatric Neurosurgery

Neurotrauma Society of India

Skull Base Surgery Society of India

Society of Pharmacovigilance (India)

Asian Congress of Neurological Surgery

Asian Australasian society of Neurological Surgeons.

Dr. V K Jain has been serving as an Editorial Board Member of the Journal of Postgraduate Medicine, Mumbai, Neurology India, the Official Journal of Neurological Society of India, Indian Journal of Neurotrauma, Spine, Surgical Neurology International.

He has also been appointed as a keynote speaker for numerous events around the world. He has been invited to function as a professor at numerous conventions, venues, and seminars both in India and abroad.

Work Experience

41 years of experience in Neurosurgery

Currently, Principal Director at Department of Neurosurgery at Max Hospitals in Delhi and NCR region

Chairman of the Neurosurgery Department, Sir Ganga Ram Hospital, since February 2010

Prof. at SGPGIMS, Lucknow, from Apr 1999 to Feb 2010

Visiting Professor at University Hospital of Geneva, Geneva, Switzerland from 15th to 30th June 2001

Visiting Professor at Fujita Gakuen Health University, Toyoake, Aichi, Japan from 03.05.1999 to 29.05.1999

Additional Prof. at SGPGIMS, Lucknow, September 1987 to April 1999

Associate Prof. at NIMHANS, Bangalore, December 1984 to September 1987

Assistant Prof. at NIMHANS, Bangalore, September 1981 to December 1984

Research Papers & Publications

Dr. Jain has numerous publications to his name.

His book — “Craniovertebral Junction Anomalies — The Indian Experience“, was published in 1997 and is still a useful guide to the medical industry.

In 2018, he co-edited a book on “Craniovertebral Junction Disorders”.

His opinions have also been featured in books on various aspects of Neurosurgery.

His articles regarding Neurology and Neurosurgery have been featured in many publications such as Surgical Neurology, Journal of Neurosurgery, Neurosurgery, Neurology India, Indian Journal of Neurotrauma etc.

Dr. Jain is a highly respected and highly esteemed figure in the medical world due to his contributions in teaching and research. He is highly respected and loved by his patients as he is very patient and family oriented for his patients and always there for them despite his busy schedule.

If you have any sort of neuro and spinal issues, do not hesitate to schedule an appointment with Dr. VK Jain.

Tags= Spine Specialist in India, Best Neuro Surgeon in India, Neurosurgeon in India, Spine Surgeon in India, Neurologist in India

[sudheervanguri]

IQVIA Hiring Regulatory Affairs Specialist IQVIA, a global leader in advanced analytics, technology solutions, and clinical research services to the life sciences industry, is seeking a Regulatory Affairs Specialist to join their team in Mumbai, Maharashtra. This is a full-time position offering an exciting opportunity for professionals with experience in Pharmacovigilance or Regulatory Affairs to make a significant impact in the field of drug safety and regulatory compliance. Job Responsibilities As a Regulatory Affairs Specialist, you will be responsible for managing and maintaining drug safety data in the European Medicines Agency's EudraVigilance database. Your key responsibilities will include: Job Description of a XeVMPD Associate: Data Management: Responsible for entering and updating information about medicinal products in the XeVMPD system in accordance with EU regulatory guidelines. Quality Assurance: Ensures the accuracy and quality of data entered into the system. Regularly reviews and cleans data to maintain its integrity. Regulatory Compliance: Ensures compliance with all relevant regulatory guidelines related to XeVMPD. Keeps up-to-date with changes in regulations and implements them in data management practices. Collaboration: Works closely with other departments, such as Regulatory Affairs and Pharmacovigilance, to collect necessary information and ensure its correct entry into the system. Reporting: Generates regular reports on data management activities and presents findings to relevant stakeholders. Training: May be responsible for training other team members on XeVMPD data entry and management practices. Problem Solving: Addresses and resolves any issues or discrepancies in the XeVMPD data promptly. Requirements for this role typically include a degree in Pharmacy, Life Sciences, or a related field, along with experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail, knowledge of EU regulations related to drug safety, and proficiency in data management systems are also essential. [caption id="attachment_84783" align="aligncenter" width="1200"] IQVIA Hiring Regulatory Affairs Specialist[/caption] Qualifications To be considered for this role, you should have: A degree in Pharmacy, Life Sciences, or a related field. Experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail. Knowledge of EU regulations related to drug safety. Proficiency in data management systems. Requirements for this role typically include a degree in Pharmacy, Life Sciences, or a related field, along with experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail, knowledge of EU regulations related to drug safety, and proficiency in data management systems are also essential. How to Apply If you meet the qualifications and are excited about the opportunity to work with a global leader in the life sciences industry, we encourage you to apply online through the following link: IQVIA Application Portal.

[resoveitech]

Pharmacovigilance training: Wouldn't it be less expensive not to disturb?

Even large pharmaceutical companies are struggling to find the right expertise internally if you search Google for "pharmacy caution," it will show you how desperate this shortage is. This lack of talent brings the resulting problems when they are inspected by the competent authorities; such inspections are an inevitable part of the process of pharmacovigilance. The requirements of SMEs cannot meet their financial needs internally, and they should subcontract parts or all of the vigilance and safety of medicines. They then try to find a reliable supplier of pharmacovigilance that they can trust.

For small and medium-sized pharmaceutical companies, the cost of administering a vigilant drug regimen is prohibitive: they simply cannot afford it, whatever the value and the task. For large companies, Pharmacovigilance training systems may be something that would like to outsource for efficiency reasons. There are many contracting organizations that can operate the drug alert system for you. Again, there are many factors to consider, and the cost is only one of them.

Through a sub-contracted pharmacovigilance system, the regulator will be held responsible for any problems in place of the contracting company, so you will need to make sure that the staff are well trained and master the relevant languages you will need, especially English. They will receive and process reports from medical professionals, expedite them when necessary, add them to the Medication Alert database, treat them and connect with medical professionals and regulatory bodies on their behalf as well as receive calls and inquiries from members of the public. Remember that when any member of your company or company detects a potentially serious adverse reaction, you have 15 days to confirm this report and send it to the organizer. Outsourcing is a serious issue. Your marketing permission depends on it. What steps do you take to ensure that the outsourcing of pharmacovigilance is validated and compliant? Is the qualified person available at all times when necessary? Do they have experience in answering the questions of the organizers?

There are many companies that provide pharmacovigilance services, but very few of them have been established as research institutions for pharmacovigilance contracts by some people working in the industry from the beginning. Pharmacovigilance training in Mumbai was created as a joint venture between Ergomed and CRO and Elliot Brown Consulting, whose managing director was an author of MedDRA, the medical dictionary of regulatory authorities, and is now used worldwide by all regulators and pharmaceutical companies and, more recently, the World Health Organization. Pietrek Associates offers a similar consulting service. The other option is to go with one of the larger CROs like Parexel, but costs with companies like these can be prohibitive.

[clininfotechseo]

Best Pharmacovigilance course in Bangalore | Clininfotech

The Pharmacovigilance Certification course is a three-month program that includes two months of training and one month of internship. This course provides you with practical, hands-on experience that allows you to complete real-world projects with ease. If you want the best Pharmacovigilance course in Bangalore? Then you are at the right destination. Clin Infotech offers the best Pharmacovigilance course in Bangalore. For more details about the course, visit our website.

[anamikasing]

Clinical Research Courses Opens the Door to Numerous Career Opportunities

Aim of the clinical research sector

Clinical Research is considered to be a vital branch in the field of healthcare sciences. The main purpose of the clinical research sector is to discover study and verify the clinical and pharmacological advantages of pharmaceutical products such as medications, diagnosis regimes and devices.

Clinical Research Courses Equip professionals with the skills

When novel drugs need to be manufactured and made available in the market for the general public, there is a certain standard as well as code of ethics that must be complied by pharmaceutical organizations. In order to train professionals in the field of clinical research, several institutes offer Clinical Research Courses to equip them with the skills to carry out extensive clinical research and maintain the standards of a clinical trial.

The clinical research industry is very productive and is growing at a rapid rate. With this rate of growth, large numbers of career opportunities are available to pharmaceutical, medical and all the interdisciplinary fields. To illustrate, more than 400 large and small clinical research organizations have now opened their doors in big cities such as Hyderabad, Chandigarh, Delhi, Gurgaon, and Mumbai.

Rewarding opportunities in Pharmaceutical industries

There are countless opportunities for clinical researchers for a wide range of clinical trials. Therefore one can get innumerable opportunities in various pharmaceutical companies after completing Clinical Research Courses in the clinical research industry.

https://www.technobridge.in/clinical-research-course.html

Countless opportunities in the clinical research sector

Apart from pharmaceutical industries, one could get various job opportunities after completing clinical research training and courses in other industries. One could either work in hospitals, health research industries, government agencies or various research organizations. The job profiles of a clinical researcher may vary with respect to the different organizations.

Candidates in the clinical research sector have infinite choices in thePharmaceutical industry after successful completion of Diploma in Clinical Research. The pharmaceutical industry conducts several clinical trials across a wide range of industries therefore clinical research professionals are capable to enter into various sectors namely. Pharmaceutical, Biotechnology, Clinical CRO, Pharmacovigilance, Clinical Data Management, IT companies in healthcare, Central laboratories, and data management in clinical research organizations.

The qualification that would be preferred for a candidate to pursue a Clinical Research Courses is a degree in zoology, botany, or biochemistry. One can start a career in the clinical research sector by pursuing Clinical Research Courses from a reputed institute. At the same time, a professional needs to have a good understanding of the field and ability to carry out the wide range of tasks that are assigned to them in the clinical research field. Pursuing a career in clinical research is a dream of many and in order to get an opportunity, one must enroll for the Clinical Research Courses with a reputed institute.

https://www.technobridge.in/

[digitalyesweus]

Crimson Consultancy Services!

The industry of clinical trials and research has been experiencing a high rise in India and so is the case with the clinical research training institutes. Most of the students are now opting for the clinical research and project management courses. The pharmaceutical industries are looking for professionals in the department of pharmacovigillance. Crimson provides both training as well as consulting services and is recognized as one of the best choices for conduction clinical research programs.

Crimson consultancy services is one organization that provides training to students in the areas of clinical research, therapeutic monitoring. It is best known for the training of Project management of clinical trials in India. It is one among the most popular clinical research training institutes based in Mumbai. The services offered during the project management training are audit queries, contract management, timeline tracking, report reviewing and submitting and feasibility studies.

Crimson provides wide variety of both part time and full time online courses. The team of professionals of Crimson Consultancy services provide clinical research training services in various fields like Diabetes Mellitus, Cancer studies, cardio-vascular diseases, CNS related disorders etc. The organization also provides training for development of soft skills and ethical skills which most of the other institutes do not provide. Intense soft skill development program is planned so as to improve the candidate’s interpersonal skills, interview skills, body language, etiquette, personality development, development of communication skills, etc.

The students willing to pursue the training program at Crimson Consultancy Services are offered with multiple career options and guidance from the team of experts. The team ensures to provide 100% placement in top reputed companies. The company has collaborations with the many reputed pharmaceutical companies of clinical research and cosmeceutical companies.

[sudheervanguri]

IQVIA Hiring Regulatory Affairs Specialist IQVIA, a global leader in advanced analytics, technology solutions, and clinical research services to the life sciences industry, is seeking a Regulatory Affairs Specialist to join their team in Mumbai, Maharashtra. This is a full-time position offering an exciting opportunity for professionals with experience in Pharmacovigilance or Regulatory Affairs to make a significant impact in the field of drug safety and regulatory compliance. Job Responsibilities As a Regulatory Affairs Specialist, you will be responsible for managing and maintaining drug safety data in the European Medicines Agency's EudraVigilance database. Your key responsibilities will include: Job Description of a XeVMPD Associate: Data Management: Responsible for entering and updating information about medicinal products in the XeVMPD system in accordance with EU regulatory guidelines. Quality Assurance: Ensures the accuracy and quality of data entered into the system. Regularly reviews and cleans data to maintain its integrity. Regulatory Compliance: Ensures compliance with all relevant regulatory guidelines related to XeVMPD. Keeps up-to-date with changes in regulations and implements them in data management practices. Collaboration: Works closely with other departments, such as Regulatory Affairs and Pharmacovigilance, to collect necessary information and ensure its correct entry into the system. Reporting: Generates regular reports on data management activities and presents findings to relevant stakeholders. Training: May be responsible for training other team members on XeVMPD data entry and management practices. Problem Solving: Addresses and resolves any issues or discrepancies in the XeVMPD data promptly. Requirements for this role typically include a degree in Pharmacy, Life Sciences, or a related field, along with experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail, knowledge of EU regulations related to drug safety, and proficiency in data management systems are also essential. [caption id="attachment_84783" align="aligncenter" width="1200"] IQVIA Hiring Regulatory Affairs Specialist[/caption] Qualifications To be considered for this role, you should have: A degree in Pharmacy, Life Sciences, or a related field. Experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail. Knowledge of EU regulations related to drug safety. Proficiency in data management systems. Requirements for this role typically include a degree in Pharmacy, Life Sciences, or a related field, along with experience in Pharmacovigilance or Regulatory Affairs. Strong attention to detail, knowledge of EU regulations related to drug safety, and proficiency in data management systems are also essential. How to Apply If you meet the qualifications and are excited about the opportunity to work with a global leader in the life sciences industry, we encourage you to apply online through the following link: IQVIA Application Portal.