Global Certificate in Clinical Trials and Research Management

Monday, 16 February 2026 10:00:48

International applicants and their qualifications are accepted

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Overview

Overview

Global Certificate in Clinical Trials and Research Management

Designed for professionals in the pharmaceutical and biotechnology industries, this certificate program equips learners with the knowledge and skills required to manage clinical trials and research studies.


Some key areas of focus include clinical trial design, regulatory compliance, and data management, all of which are essential for successful trial execution.


Through a combination of online courses and hands-on training, learners will gain a deep understanding of the clinical trials process and be able to apply their knowledge in real-world settings.


Whether you're looking to advance your career or start a new one, this certificate program can help you stay ahead of the curve in the rapidly evolving field of clinical trials and research management.


So why wait? Explore the Global Certificate in Clinical Trials and Research Management today and take the first step towards a successful career in this exciting field.

Global Certificate in Clinical Trials and Research Management is an ideal course for those seeking to launch a career in the pharmaceutical industry. This comprehensive program offers key benefits such as hands-on experience, industry connections, and a globally recognized certification. Upon completion, you'll be equipped with the skills to manage clinical trials, analyze data, and navigate regulatory requirements. The course features unique features like project management, research design, and quality assurance. Career prospects are excellent, with job opportunities in pharmaceutical companies, research institutions, and consulting firms. With a global perspective, you'll be prepared to work in diverse environments.

Entry requirements

The program operates on an open enrollment basis, and there are no specific entry requirements. Individuals with a genuine interest in the subject matter are welcome to participate.

International applicants and their qualifications are accepted.

Step into a transformative journey at LSIB, where you'll become part of a vibrant community of students from over 157 nationalities.

At LSIB, we are a global family. When you join us, your qualifications are recognized and accepted, making you a valued member of our diverse, internationally connected community.

Course Content

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• Clinical Trial Management System (CTMS)
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• Good Clinical Practice (GCP)
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• Clinical Research Coordinator (CRC)
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• Clinical Trial Protocol
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• Informed Consent Form (ICF)
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• Data Management Plan (DMP)
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• Quality Assurance (QA) in Clinical Trials
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• Regulatory Compliance in Clinical Trials
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• Clinical Trial Supply Management
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• Study Start-Up and Close-Out

Assessment

The evaluation process is conducted through the submission of assignments, and there are no written examinations involved.

Fee and Payment Plans

30 to 40% Cheaper than most Universities and Colleges

Duration & course fee

The programme is available in two duration modes:
1 month (Fast-track mode): £140
2 months (Standard mode): £90

40% Cheaper

Our course fee is up to 40% cheaper than most universities and colleges.

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Awarding body

 The programme is awarded by London School of International Business. This program is not intended to replace or serve as an equivalent to obtaining a formal degree or diploma. It should be noted that this course is not accredited by a recognised awarding body or regulated by an authorised institution/ body.

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  • Start this course anytime from anywhere.
  • 1. Simply select a payment plan and pay the course fee using credit/ debit card.
  • 2. Course starts
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Got questions? Get in touch

Chat with us: Click the live chat button

+44 75 2064 7455

admissions@lsib.co.uk

+44 (0) 20 3608 0144



Career path

Key facts about Global Certificate in Clinical Trials and Research Management

The Global Certificate in Clinical Trials and Research Management is a comprehensive program designed to equip individuals with the knowledge and skills required to manage clinical trials and research studies effectively.
This certificate program is ideal for professionals working in the pharmaceutical, biotechnology, and medical device industries, as well as researchers, clinical trial managers, and study coordinators.
The program covers a wide range of topics, including clinical trial design, regulatory compliance, data management, and quality assurance, ensuring that graduates are well-equipped to manage clinical trials from start to finish.
Upon completion of the program, graduates can expect to gain a deeper understanding of the clinical trials process, including the ability to identify and mitigate risks, optimize study timelines, and ensure compliance with regulatory requirements.
The duration of the Global Certificate in Clinical Trials and Research Management varies depending on the institution offering the program, but most programs take around 6-12 months to complete.
Industry relevance is high for this certificate, as the demand for skilled clinical trial managers and researchers continues to grow.
Many organizations, including pharmaceutical companies, contract research organizations (CROs), and research institutions, require or prefer candidates with this level of expertise.
The Global Certificate in Clinical Trials and Research Management is a valuable asset for anyone looking to advance their career in this field, and can be completed online or on-site, making it accessible to professionals worldwide.
With its comprehensive curriculum and industry-recognized certification, this program is an excellent choice for individuals seeking to launch or enhance their careers in clinical trials and research management.

Why this course?

Global Certificate in Clinical Trials and Research Management holds immense significance in today's market, particularly in the UK. The UK's National Institute for Health Research (NIHR) has reported a significant increase in clinical trials, with over 3,500 trials conducted in 2020 alone. This growth is driven by the need for innovative treatments and therapies, as well as the increasing importance of research management in ensuring the smooth conduct of trials.
Year Number of Trials
2015 2,500
2018 3,000
2020 3,500

Who should enrol in Global Certificate in Clinical Trials and Research Management?

Ideal Audience for Global Certificate in Clinical Trials and Research Management Professionals working in the pharmaceutical, biotechnology, and medical device industries, particularly those involved in clinical trials, research management, and regulatory compliance, are the primary target audience for this certificate.
Key Characteristics: Individuals with a bachelor's degree in life sciences, healthcare, or a related field, with at least 2 years of experience in clinical trials or research management, are well-suited for this certificate. In the UK, this may include professionals working in the NHS, pharmaceutical companies, or contract research organizations (CROs).
Career Goals: The certificate is designed to enhance career prospects for those seeking to transition into research management, clinical trials coordination, or regulatory affairs roles. In the UK, this may include individuals looking to advance their careers in the NHS, pharmaceutical industry, or CROs, with median salaries ranging from £40,000 to £70,000 per annum.
Learning Outcomes: Upon completion of the certificate, learners can expect to gain knowledge and skills in clinical trials management, research design, regulatory compliance, and data analysis, enabling them to make informed decisions in their careers and contribute to the success of clinical trials and research programs.