How is Clinical Research used?
Zippia reviewed thousands of resumes to understand how clinical research is used in different jobs. Explore the list of common job responsibilities related to clinical research below:
- Direct and manage a rare disease patient registry designed to integrate human subjects into clinical research projects.
- Created and implemented Clinical Research Billing Office to ensure compliance with research billing regulations.
- Created business plans for creation of clinical research spin-off company designed to organize and carry out clinical research in community hospitals.
- Formed nutritional and clinical research partnerships with 2 independent optometrists in the local community.
- Designed and conducted exercise protocols for clinical research trials involving osteoarthritis in humans.
- Developed and implemented all clinical, administrative, financial, IT, and compliance elements of the MWMC clinical research enterprise.
Are Clinical Research skills in demand?
Yes, clinical research skills are in demand today. Currently, 14,614 job openings list clinical research skills as a requirement. The job descriptions that most frequently include clinical research skills are research/program director, research kennel supervisor, and clinical research scientist.
How hard is it to learn Clinical Research?
Based on the average complexity level of the jobs that use clinical research the most: research/program director, research kennel supervisor, and clinical research scientist. The complexity level of these jobs is challenging.
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What jobs can you get with Clinical Research skills?
You can get a job as a research/program director, research kennel supervisor, and clinical research scientist with clinical research skills. After analyzing resumes and job postings, we identified these as the most common job titles for candidates with clinical research skills.
Research/Program Director
- Research Program
- Oversight
- Clinical Research
- Research Projects
- Professional Development
- Clinical Trials
Research Kennel Supervisor
- Clinical Research
- Research Projects
- R
- Data Collection
- Research Studies
- IRB
Clinical Research Scientist
Job description:
A clinical research scientist is responsible for assisting physicians in conducting laboratory research and examinations to identify diseases and establish treatment plans. They also inspect medical tools and equipment to prevent hazards and operational delays. A clinical research scientist must have excellent communication skills and extensive knowledge of the medical industry to provide the highest quality care services for the patients.
- Clinical Research
- Clinical Trials
- Clinical Development
- Data Management
- Oncology
- Clinical Data
Scientific Director
Job description:
A scientific director is primarily in charge of spearheading and overseeing the researching programs in an institution, medical facility, or company. It is their duty to set goals and objectives, hire researchers and other experts, establish guidelines, liaise with sponsors and key personnel, and develop strategies to optimize laboratory procedures. Furthermore, as a scientific director, it is essential to lead and encourage the workforce to reach goals, all while implementing the policies and regulations of the organization, including its vision and mission.
- Medical Affairs
- Clinical Development
- Clinical Research
- Pharmaceutical Industry
- FDA
- Immunology
Clinical Trials Specialist
Job description:
A Clinical Trials specialist assist in the daily activities involved in clinical trials. This includes gathering facts, information, and observed data and helps analyze and interpret results. Clinic trials are essential in developing new medicines and vaccines needed for the safeguard of human health. Alongside this primary responsibility, it is also the clinical trial specialist's task to organize data, monitor laboratory equipment, and ensure all specimens needed for the trials are according to instructions.
- Patients
- Clinical Research
- Clinical Trials
- Informed Consent
- FDA
- Consent Forms
Cancer Researcher
Job description:
A cancer researcher is a medical scientist who devotes their time working at laboratories to study and discover ways to diagnose and treat cancer, saving countless people's lives in the process. Their duties usually include gathering and analyzing samples through basic or complex laboratory processes, studying existing cases from people of all ages, organizing specimens and instruments, coordinating with fellow experts, conducting experiments, and maintaining extensive records. Moreover, as a cancer researcher, it is essential to keep an open communication line with fellow researchers, collaborating efforts for a smooth workflow.
- Patients
- Clinical Research
- Clinical Trials
- Data Collection
- Patient Care
- Informed Consent
Research Compliance Specialist
- Human Subjects
- Research Compliance
- IRB
- Clinical Research
- Federal Regulations
- Informed Consent
Clinical Project Manager
Job description:
A clinical project manager specializes in developing and organizing clinical trials. Their responsibilities revolve around planning and coordinating with all necessary personnel and experts, scheduling meetings, and preparing necessary documentation, ensuring compliance with all laws and regulations. Moreover, a clinical project manager must devise strategies and train all staff, develop protocols and guidelines, coordinate with vendors and suppliers, evaluate staff and verify documentation, and assist in all activities to ensure that every process aligns with the project's agenda. Should there be any issues or concerns, a clinical project manager must conduct corrective measures right away.
- Manage Cross
- Patients
- Clinical Research
- Project Management
- Clinical Trials
- Oversight
Clinical Data Management Manager
Job description:
Clinical data management managers perform database development tests to support the clinical studies assigned to them. These managers must have collaboration and communication skills to work smoothly with other internal departments and fellow managers. They lead problem-solving in data collection, quality control, and improving their current data management process. Their job is to become a model that works and reinforces their company's vision and mission. They also ensure those project deadlines are met by organizing and distributing workloads and schedules to the staff.
- GCP
- Data Management
- Clinical Research
- CRO
- Data Collection
- FDA
Clinical Trial Manager
Job description:
A clinical trial manager is primarily responsible for organizing and supervising clinical trials, ensuring to meet all goals while maintaining smooth operations. They are also responsible for collaborating with managers to set targets, hiring staff and participants for studies, and arranging the event. This planning includes its location and schedule. A clinical trial manager must also maintain documentation of all processes, liaise with scientists and key personnel, acquire necessary legal paperwork and certifications, and gather data accurately. Furthermore, as a manager, it is essential to implement the company's policies and regulations at all times.
- Patients
- Clinical Trial Management
- Clinical Operations
- Clinical Research
- Oversight
- Project Management
Medical Writer
Job description:
As the name entails, medical writers produce technical, educational, promotional, and technical content. They typically work with physicians, scientists, and subject matter experts to produce documentation that defines product usage and research results. Their duties and responsibilities may vary, but they perform some common tasks, including developing documentation related to clinical trials, creating monographs, and developing promotional materials. Medical writers are also responsible for creating grant proposals, writing newspaper and magazine articles, and creating presentations for conferences.
- Medical Writing
- Patients
- Clinical Research
- Clinical Study Reports
- Literature Searches
- FDA
Senior Medical Writer
Job description:
A Senior Medical Writer is responsible for writing comprehensive medical texts and composition for various audiences according to required themes and subjects. Senior Medical Writers maintain the accuracy and authenticity of all information by coordinating with medical professionals and other related parties to gather data. They also study recent trends and innovations within the medical industry and share findings with the clients for further study. A Senior Medical Writer must have excellent communication and leadership skills, especially in training junior writers and setting recommendations for high-quality publications.
- Medical Writing
- Clinical Data
- Clinical Study Reports
- Clinical Research
- FDA
- Patients
Program And Research Coordinator
Job description:
Research and program coordinators are responsible for helping with the establishment of research data from laboratory investigations and clinical trials with the administration of a research supervisor or a lead researcher. Their duties include leading field investigations and evaluating existing research materials after realizing the scope and limitations of the study. They record their results and valuable resources on the research database as sources to the research team. Research and program coordinators must have excellent communication skills, both written and oral, especially generating data and collaborating with other researchers for the progress and improvement of the study.
- Patients
- Research Program
- IRB
- Informed Consent
- Clinical Research
- Research Data
How much can you earn with Clinical Research skills?
You can earn up to $77,858 a year with clinical research skills if you become a research/program director, the highest-paying job that requires clinical research skills. Research kennel supervisors can earn the second-highest salary among jobs that use Python, $71,298 a year.
| Job title | Average salary | Hourly rate |
|---|---|---|
| Research/Program Director | $77,858 | $37 |
| Research Kennel Supervisor | $71,298 | $34 |
| Clinical Research Scientist | $99,160 | $48 |
| Scientific Director | $116,045 | $56 |
| Clinical Trials Specialist | $74,910 | $36 |
Companies using Clinical Research in 2025
The top companies that look for employees with clinical research skills are Johnson & Johnson, Merck, and QuintilesIMS. In the millions of job postings we reviewed, these companies mention clinical research skills most frequently.
| Rank | Company | % of all skills | Job openings |
|---|---|---|---|
| 1 | Johnson & Johnson | 16% | 1,424 |
| 2 | Merck | 14% | 1,709 |
| 3 | QuintilesIMS | 8% | 1,471 |
| 4 | Takeda Pharmaceuticals U.S.A., Inc. | 8% | 1,510 |
| 5 | Florida Cancer Specialists & Research Institute | 6% | 659 |
Departments using Clinical Research
| Department | Average salary |
|---|---|
| Healthcare | $78,496 |
| Research & Development | $63,215 |
12 courses for Clinical Research skills
1. Fundamentals of Clinical Research
Welcome to the Fundamentals of Clinical Research course, a comprehensive guide designed to equip you with the foundational knowledge and practical skills required to excel in the realm of clinical research. This course, brought to you by the esteemed Alpha Research Organization (ARO), is divided into five exhaustive units that delve into the intricacies of clinical research. Unit 1 begins by providing an overview of the research process, setting the stage for what lies ahead. Here, we'll walk you through how to identify and define a research problem, and the techniques for conducting an exhaustive literature search to understand the current landscape around your chosen problem. Unit 2 builds on the first unit by introducing you to different study designs used in clinical research. Each design has its strengths and weaknesses, and a clear understanding of these will allow you to select the most appropriate one for your study. We'll also delve into the concept of bias, exploring its sources and discussing strategies to control it. In Unit 3, we help you develop the necessary skills to read, deconstruct, and critically appraise scientific papers, a crucial competency in the research field. This unit also includes adiscussion on the ethics of conducting research, ensuring you understand the importance of integrity and respect for subjects' rights and welfare. Unit 4 introduces you to the world of statistics, a powerful tool integral to interpreting and communicating research findings. We also cover how to design and implement surveys, an essential method of data collection in many research scenarios. Finally, in Unit 5, we explore the concept of Evidence-Based Medicine (EBM) and provide a roadmap on how to conduct and interpret cross-sectional and systematic reviews. Understanding EBM allows you to integrate best research evidence into clinical decision making, while gaining proficiency in these review methods will enhance your ability to synthesize a body of research on a particular topic. Whether you are a student in healthcare, a budding researcher, a practicing professional, or simply someone with a deep interest in understanding how clinical research is conducted, this course will offer a rigorous and engaging learning journey. Our dedicated and experienced instructors at ARO will ensure that by the end of this course, you will have a robust understanding of the fundamentals of clinical research, empowering you to contribute effectively to the field. Enroll today, and take a step towards becoming a proficient clinical researcher. Aim of the Course: The primary aim of the Fundamentals of Clinical Research course is to provide a comprehensive understanding of the core elements of clinical research, equip students with the necessary skills to conduct, interpret, and appraise clinical studies, and foster ethical and responsible research practices. Objectives of the Course: By the end of the Fundamentals of Clinical Research course, students will be able to: Understand the research process: Identify and articulate a clear research problem and understand the necessity and techniques for a comprehensive literature search. Select appropriate study designs: Understand different types of study designs, their applicability, and their potential strengths and weaknesses. Manage bias: Identify various sources of bias in research and learn strategies to minimize their impact on the research outcomes. Critically appraise scientific literature: Develop the skills needed to deconstruct, analyze, and critique scientific papers. Adhere to ethical research practices: Recognize the importance of ethics in research and uphold ethical principles in all aspects of clinical research. Apply statistics in research: Understand the fundamentals of statistics in interpreting and representing research data. Design effective surveys: Learn how to develop and implement surveys as tools for data collection in research. Implement Evidence-Based Medicine (EBM): Grasp the principles of EBM and learn how to integrate best research evidence into clinical decision making. Conduct cross-sectional and systematic reviews: Understand the methodologies of conducting and interpreting cross-sectional and systematic reviews. Synthesize learning: Apply the knowledge and skills acquired throughout the course to conduct a comprehensive and ethically sound research study...
2. Clinical Research for beginners
Welcome to this course on Clincal Research Methodology. I have designed this course so that even beginners can learn how to do reserch in a methodical way and publish impactful papers. You will come across examples from real research topics in various modules to grasp the subject better. I recommend that you try the Practice test before starting the lectures and take the test again after finishing the course to know how much you have imbibed from the lectures In the Overview module, we will learn the advantages of doing good scientific research and publications and you will see glimpses of my journey from being a medical student to coming of age as a researcher. I believe that If I could do it, then so can you. In the module on Literature review, we will go through how to utilize and customize PubMed in the best possible manner for your individual requirements, how to get fresh ideas for research topics and nuances of study designs. In the Biostatistics module, we will build up concepts from the very basics such as What is a variable till basic understanding of advanced statistics. You will get exposed to topics like How to make an effective Excel sheet and How to communicate with a biostatistician Manuscript writing can be daunting. In the module on Manuscript writing, you will learn to use some templates that will simplify your job and make the writing process enjoyable. Each 10-minute lecture is packed with information in a very lucid manner enabling you to grasp concepts while enjoying the learning process. Learn on the go and access lectures on your device anytime anywhere. Lectures feature myself on screen speaking with you directly as well as intermittent slides to enhance the learning experience. It will feel like a LIVE one - on - one lecture. I hope that this will be a fruitful and exciting learning experience for you and I look forward to having you here. At the end, you will be able to design studies including randomized clinical trials, do a good literature search, understand relavant biostatistics and write meaningful manuscripts that can be published in high impact journals. Additionally, you will also be able to interpret the merits of published literature and apply knowledge to improve patient care...
3. Good Clinical Practice for Clinical Research Professionals
Updates: September 2023: Updated section of ICH GCP R3 Draft Principles and added resource documentationAugust 2023: Added list of Acronyms and Abbreviations used in the course (section 1)June 2023: Added DRAFT ICH GCP (R3) Annexe 1 (interventional clinical trials), its summary of changes and explanatory video in the resources. This version is made available by the ICH for public consultation until September 2023 (step 2 of the ICH process)May 2023: Added link to ICH E8 (R1) in resources of quality managementFebruary 2023: Added awareness of the most common GCP findings (lecture 4)January 2023: Edited English subtitles, adding French subtitlesDecember 2022: Added assignment: Practical risk assessment based on UK MHRA inspection report (section 11)October 2022: Added assignment: Practical exercises from real FDA inspection cases (section 10)September 2022: Added updates on ongoing development of Revision 3 of ICH-GCP (section 12)-Welcome to the only up-to-date, complete edition of the ICH GCP course! This course meets the Minimum Criteria for ICH E6 (R2) GCP Investigator and Site Personnel Training that TransCelerate has identified as necessary to enable mutual recognition of GCP training. This course offers the first professional, fundamental on-line ICH GCP (R2) detailed course for Investigators, Study Coordinators, Sponsors, Clinical Project Managers, Monitors and any other Clinical Study staff requiring knowledge in GCP for a successful execution your clinical trials. This ICH-GCP course also presents elements of ICH GCP E6 (R3) as they become available currently under revision by ICH. My name is Dr. Vincent Baeyens PhD, I have more than 20 years of experience in running Clinical Trials in Global and mid-size Pharma, and Biotech settings. I have worked with most of the Global as well as several niche CROs and I am also an expert in CRO Management and Oversight, budgeting and Risk Management. In this course, you will be able to understand based on my experience the key ICH GCP requirements to design, conduct, record and report clinical trials in humans from A to Z. We will review the role and responsibilities of the key stakeholders and the structure of the essentials documents. To facilitate the learning of beginner students, the course has been broken up on purpose in several small lectures. Note: If you are a more advanced student, you can increase the speed of lecture to learn the course at your own pace. This course will provide you with a strong support to prepare for successful regulatory ICH GCP inspections and audits. I will lead you step-by-step through the ICH GCP E6, and you will learn & understand: What is GCP and why GCP is important in clinical researchThe link between the Declaration of Helsinki and current GCPThe definition of the key definitions of terms and concepts used in clinical research, including stakeholders involved and essential documentsThe ICH GCP Principles of Revision 2 and Revision 3 and practical advices to apply them in your clinical trialsThe responsibilities of ethics committees, its composition, function, operational aspects and obligationsThe detailed responsibilities of the Investigator throughout the trial, including his/her qualifications, compliance to protocol, communication with Ethics Committees, safety reporting, and final reportingHow to write an adequate Protocol / protocol amendment and rationale for its structureThe What, the Why and the How for an effective writing of the Investigator's BrochureThe purpose of Essential Documents in clinical research: How and Where to file them in the Trial Master File (TMF)The common ICH GCP audit and inspection findings in clinical trials with practical exercises (FDA, MHRA)I will illustrate the GCP concepts with several practical tips & tricks , so that you will be able to apply ICH GCP to your daily practice from Day 1! Quizzes are proposed to test your knowledge along your journey. A final Quiz at the end of the course will consolidate your knowledge. Feel free to look at the content of the course to know more and contact me any time if you have any questions! After the course, spend 1 hour with the EXPERT to answer ALL the questions that you would have!! All you have to do is to send me an e-mail with your questions and contact details, and I will set up a call with you. I am of course available personally during the course as well to answer your questions or comments! I am looking forward to seeing you inside the course! Sincerely, Vincent...
4. Good Clinical Practice ICH GCP for Clinical Research
***Why this course is considered as a TOP RATED and BEST SELLING course for the ICH GCP category on Udemy?***See what students are talking about in this course:5***** Star RatingI'm very glad I enrolled in this class! There's so much information to be absorbed and she did a great job in presenting everything in as much detail as possible, but at the same time simplifying it to make your learning experience a lot smoother. This is a great course if you're just starting out and want to know the fundamentals of GCP. This master class has it all! --Devon Roman5***** Star RatingShe is a great instructor, very transparent, cuts out all the BS getting straight to the meat and potatoes of the subject at hand, exactly how I like to learn. I am happy about investing in this course. The videos are over the shoulder at the right pace explaining the process of understanding the clauses. The course has left me feeling confident that I can achieve my goals, plus I had so much fun learning. If you create any more courses, you have a repeat customer in me.-- Rebecca5***** Star RatingVery well constructed course covering all the topics I was interested in. Really liked the step-by-step approach and tasks broken into manageable chunks, allowing me to absorb the information. The tutor was great, the notes were very helpful and I made a lot of use of the Quizzes and Assignments section. Highly recommend the course for either a beginner or someone with some experience but a bit rusty (such as me).-- Reshma 5***** Star RatingShe is an amazing teacher, the best I could find so far. She is knowledgeable, explains very well, has a nice and soothing voice, and has a great sense of presentation. The course is also more hands-on than a lot of other courses where you practically just watch guys read. She explains clauses practically who ICH GCP E6 document. If you want to learn and understand GCP or clinical research in general, this is a great place to start.-- Varun P5***** Star RatingThis is an excellent, cost-effective, and comprehensive course and I'm so glad to enroll in the class. Plus, I've learned so much from the basics that have been taught. I'm so grateful to have the instructor spending time to develop this course and share knowledge. Again, thanks, and this course is highly recommended!-- Dennis Clayton5***** Star RatingThe content was helpful and this was a nice quick review.-- Ayesha A. Rizvi, Ed. D.5***** Star RatingThe information is explained in a detailed manner-- Monique Brown5***** Star RatingBravo-- Tshering JAMTSHO----------------------------------------------COMPLETE COURSE DESCRIPTION: Welcome to the complete ICH Good Clinical Practices E6 R2 course. In this course, we will learn what Good clinical practices are, guidelines of what an ethical and safe trial is, the rights and importance of consent of the trial subjects, the duties of the sponsor and investigator of the trial, and much more. Basically, I will walk you through the entire GCP guidelines document step by step. My name is Warda Naz, and I will be leading you through this course. Here at Magine Solutions highly experienced instructors, engineers, and doctors with more than 10 years of experience in the industry will guide you through very high-quality online courses. At the end of the course, you will be able to understandWhat is International Council for harmonization?Aims of ICHHow was ICH established?The importance of ICH. Groups working within ICHEfficacy GuidelinesWhat are Good clinical Practices (GCP)?The link between ICH and GCPAll about the Institutional review board, investigators, sponsors, clinical trial protocol and protocol amendment, investigator's brochure, essential documents for the conduct of a clinical trial, and much more. We will also learn to understand these concepts by looking at case studies to strengthen the theoretical concepts. The ideal student for this course is anyone who wants to learn about the ICH GCP E6 document or an existing professional who wants to expand on their current skills. There are no requirements necessary to enroll. I only ask to come open-minded and ready to learn. Feel free to take a look at the course description and I look forward to seeing you inside. Thank you!!----------------------------------------------...
5. Understanding Clinical Research: Behind the Statistics
If you’ve ever skipped over the results section of a medical paper because terms like “confidence interval” or “p-value” go over your head, then you’re in the right place. You may be a clinical practitioner reading research articles to keep up-to-date with developments in your field or a medical student wondering how to approach your own research. Greater confidence in understanding statistical analysis and the results can benefit both working professionals and those undertaking research themselves. If you are simply interested in properly understanding the published literature or if you are embarking on conducting your own research, this course is your first step. It offers an easy entry into interpreting common statistical concepts without getting into nitty-gritty mathematical formulae. To be able to interpret and understand these concepts is the best way to start your journey into the world of clinical literature. That’s where this course comes in - so let’s get started! The course is free to enroll and take. You will be offered the option of purchasing a certificate of completion which you become eligible for, if you successfully complete the course requirements. This can be an excellent way of staying motivated! Financial Aid is also available...
6. Essential Documentation within Clinical Research
This comprehensive course for Essential Documents will give you all the required information you need regarding documentation required for the conduct of a clinical trial. This course will cover•Define Essential Documents and their purpose •Understand what ICH GCP E6 R2 says about Essential Documents•Investigate eTMF systems and their place in accurate storage and retrieval of Essential Documents•Understand how to archive Essential Documents according to ICH GCP standards...
7. Informed Consent in Clinical Research
This course will enable participants to have an understanding of the background and practical implications of the valid informed consent process. The knowledge and understanding gained, coupled with practical examples is intended to give participants the confidence to take a proactive role in the consent process back in the workplace...
8. Clinical Research Certificate Course 2023
A career in clinical research promises productive jobs in the country and abroad. At present, India is the most preferred hub for clinical trials among all the Asian countries. If you are looking for a Career in clinical research in India, then keep reading the description below: What is Clinical Research: The health sector is an important sector in the economy. It not only provides health care facilities but also generates great academic and career choices for aspirants. Clinical research is one such branch of study that has become very popular these days. It is the study of healthcare science that deals with research carried out on humans for improving treatments, medications, devising new methods of diagnosis and increasing knowledge on various diseases and disorders. Clinical Research refers to a study conducted to assess potential treatment and its effect on human beings. Clinical trials help us find out if medication, a device, a diagnostic product or a treatment regimen is safe and effective for use. During a trial, increasing information is gained about the treatment option, its risks and how it may work. Certification in clinical research (CCR) is meant to offer candidates a chance to obtain and develop the skill essential for effective clinical research. The program is meant to meet the high demand for qualified personnel for human clinical trials. The program enables you to know the practical features of clinical trial and its management including designing the phases, implementation, planning, regulatory and procedural guidelines, data analysis, and ethical considerations. This program is designed in such a way that it assists the aspiring candidates in learning about the bioethics that goes in a hospital or a clinic. The course curriculum is such that it provides the student with the right skills needed to assist in the preparation of presentations and manuscripts of scientific meetings and technical medicine journals. The program is built to produce quality clinical research analysts having the right skill set required to work in the clinics and hospitals. Clinical Research course opens a vast range of career options for the candidates. From working in the medicine department such as clinics and hospitals to working as a teacher or lecturer at a college, candidates can select to pursue anything they wish to. Eligibility- Any degree in Bioscience/Life Sciences such as Biochemistry, Microbiology, Genetics, Biotechnology, Botany, Zoology etc- Any degree in Medicine such as MBBS, BDS, BPT, BAMS, BHMS, BUMS etc- Any degree in Pharmacy / Pharmaceutical Sciences- Any degree in Chemistry / Biostatistics / Bioinformatics- Any degree in Nursing / Allied Health.- Students in their final year of graduation for the above courses are also eligible to apply. Clinical Research Job OpportunitiesThe latest changes in regulations have a great impact on a Clinical Research Investigator's life. Latest studies show that the Clinical Research field which is at present having business growth around 250 crores will soon have a growth of approximately 5000 crores. This profession assists investigators to end up with good income similar to doctors. A lot of research sectors such as Biotech Companies, Pharma Industries, Research Labs, etc have opened job opportunities for clinical investigators. Several types of Clinical Research positions are available and few of them include: Clinical Research Managers (CRM)Clinical Research Associate (CRA)Clinical Research Coordinator (CRO)Project ManagerCounselorsScope of Clinical Research in India and Abroad: Healthcare sectors have been growing widely, and clinical research has contributed a lot to this growth. The patient-oriented, epidemiologic, behavioural, and health service research has led to the development of many treatments, methods, and medications for various healthcare problems. This has been possible because of students of clinical research. With so many health issues in the world, clinical research has an immensely popular base among medical students. The field not only provides employment opportunities to its students, but it also saves the world by attempting clinical trials and helping in the development of new vaccines and other treatments. Health problems are all around the world, and therefore, there is an equal demand for clinical research associates and physicians internationally as well. Clinical research students can become Clinical Research Analyst, Clinical Research Physicians, Clinical Research Coordinator, Biostatistician, Clinical Research Associates, and so on. Excellent students can get recruitments in popular institutions such as AIIMS and even get jobs in foreign institutes, hospitals, and clinics. Benefits of this course1) Students can learn Basic aspects of Clinical research2) Develop proficiency in study-design exhibiting the depth and difficulty of clinical and translational science applications.3) Understand how to perform and control clinical research4) Gain knowledge about various regulatory authorities and their specification to approve marketing of healthcare products.5) Gain knowledge on the use of medical data, data evaluation, and the use of data databases.6) Build expertise in communication, problem-solving, educational approaches, research and management, associated to a clinical research. Look for course description.. Look for see you in the classThank You...
9. Certificate Course in Clinical Research (CCCR)
If you find the Clinical Research field challenging, well, in that case, this is the best course for you. The pharmaceutical industry is one of the extremely regulated industries, with several government regulations to protect public health. Therefore, the important target of the pharmaceutical industry is to develop a Drug product passing the regulatory requirements. On the other hand, regulation of drug development, manufacturing, marketing, and sales involves paradoxical objectives. It must ensure that safe and effective pharmaceutical formulations reach the public quickly while concurrently protecting against ineffective/unsafe/harmful therapies. This course will provide you with a strong understanding of the Drug development process, Clinical Research and related documents, GCP, Roles, and responsibilities of major players in Clinical Research in a summarized manner which will help to work towards shaping your career in Clinical Research. This course focuses on the following points that could make Clinical Research activities smooth without any significant delays/failures,• Basic Understanding of Clinical Research,• Major players in Clinical Research,• Historical background of US Drug Law and Regulations,• Drug Approval Process,• New Drug Development-Preclinical Steps• Investigational New Drug Application (INDA),• New Drug Application (NDA),• Abbreviated New Drug Application (ANDA),• Essential Documents,• Protocol,• Source Documents,• Informed Consent form,• Investigator's Brochure,• Case Report Form (CRF),• Inclusion-Exclusion criteria,• Sponsor,• Investigator,• Clinical Research Associate (CRA) and Clinical Research Coordinator (CRC),• Important Literature Search Websites for Clinical Research Professional,• Many more... There will be several downloadable documents so that you can follow along with them whenever you need them. This course contains Commonly Asked Questions that will help you while preparing for Clinical Research interviews. Last but not the least, this course also contains a bonus course entitled Meeting etiquettes which will help you to shape your career in which the points that must be taken into consideration while attending/conducting meetings are covered. In this course, more than 30 informative videos are included and are designed in an easily digestible format and going to take you through step by step approach to understand Clinical Research and relevant activities. I believe Quality improvement is a continuous and lifetime process. Upon completion of this course, you will be a whole different professional with improved Clinical Research knowledge which will help you to garner more respect from your team members, managers, clients, or anyone with whom you are communicating/interacting...
10. The Beginners Course for Clinical Research
Have you ever wondered what it takes to land a job in clinical research? First, you have to know what clinical research is all about and the potential jobs, and this course will give you that. This course will provide you with the essentials of clinical research in a very summarized and concise manner to understand the process and to work towards building your qualifications for a job. You will learn about Good Clinical Practices and how it influences country specific regulations, the drug development process and the phases of clinical research and post-marketing research, which are the parties responsible in clinical trials, and what are the qualifications, background, training and experience a clinical research professional needs to have. This course is also supplemented with a complete description of the most typical jobs in clinical research and the not so typical, nevertheless very important. This course is part of a series of eLearning by EduPharma and Global Research Pharma Canada, and provides credits towards the Certificate in Clinical Research and the Mater Certificate in Clinical Research and Drug Development...
11. Introduction of Clinical Research for freshers
Basics of clinical research. Learn from the start. All you want to know about clinical research basic. We have divided modules in 7 parts plus a video on drug discovery and development. These module will help you understand various aspects of clinical research. Our course include introduction to clinical research, glossary in 2 parts, ethics committee, regulatory, GCP, Data Privacy and Protection, GDPR. Our course design will provide you detail information about clinical research with highly interactive videos. Please use headphone to have better audio quality...
12. Jobs in Clinical Research and How to Qualify?
This course and workshop will allow you understand the requirements for a clinical research job, as well as identify specific job duties and responsibilities. Completing this program will provide you with a hands on tool to determine your eligibility for a job in clinical research and draw a road map for qualification. The job application process is discussed and a workshop is provided to allow start you job search. This course is divided into 10 lessons with 10 workbooks to make the learning process more effective. You will have several quizzes to help you rate your knowledge and understanding of the content...