Advanced Certificate in Pharma Clinical Trials
-- viewing nowThe Advanced Certificate in Pharma Clinical Trials is a comprehensive course designed to provide learners with in-depth knowledge of the clinical trial process in the pharmaceutical industry. This course highlights the importance of conducting reliable and ethical clinical trials, ensuring the safety and efficacy of new drugs and therapies.
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Course Details
• Pharma Clinical Trials Fundamentals: Understanding the basics of clinical trials, including their purpose, design, and phases
• Ethical Considerations: Exploring the ethical issues surrounding clinical trials, such as informed consent, patient safety, and data privacy
• Regulatory Affairs: Navigating the complex regulatory landscape of clinical trials, including FDA regulations and ICH guidelines
• Clinical Trial Protocol Development: Designing and implementing a clinical trial protocol, including study objectives, endpoints, and statistical analysis plans
• Site Selection and Management: Identifying and managing clinical trial sites, including site feasibility, investigator selection, and site monitoring
• Data Management and Analysis: Collecting, managing, and analyzing clinical trial data, including data validation, statistical analysis, and data reporting
• Pharmacovigilance and Safety Monitoring: Monitoring and reporting adverse events in clinical trials, including safety signal detection, risk management, and benefit-risk assessment
• Quality Assurance and Quality Control: Ensuring the quality of clinical trial data and processes, including audits, inspections, and corrective action plans
Career Path
Clinical Trial Manager: A Clinical Trial Manager oversees the planning, execution, and reporting of clinical trials. They ensure that studies are conducted ethically, safely, and within legal requirements. The UK job market for Clinical Trial Managers is growing, with a salary range typically between £35,000 and £60,000 per year.
Clinical Research Associate: A Clinical Research Associate (CRA) coordinates and manages clinical trials and studies. They work closely with physicians, clinicians, and other healthcare professionals to ensure trials are conducted accurately. The UK job market for CRAs is strong, with a salary range between £27,000 and £50,000 per year.
Pharmacovigilance Specialist: Pharmacovigilance Specialists are responsible for monitoring, assessing, and reporting potential adverse effects or side effects of drugs during clinical trials. The UK job market for Pharmacovigilance Specialists is growing, with a salary range between £30,000 and £60,000 per year.
Biostatistician: Biostatisticians analyze and interpret data from clinical trials. They work closely with other professionals to ensure data is accurate and reliable. The UK job market for Biostatisticians is growing, with a salary range between £30,000 and £70,000 per year.
Clinical Data Manager: Clinical Data Managers are responsible for the collection, management, and analysis of clinical trial data. They design and implement data management systems and processes to ensure data quality. The UK job market for Clinical Data Managers is growing, with a salary range between £30,000 and £60,000 per year.
Entry Requirements
- Basic understanding of the subject matter
- Proficiency in English language
- Computer and internet access
- Basic computer skills
- Dedication to complete the course
No prior formal qualifications required. Course designed for accessibility.
Course Status
This course provides practical knowledge and skills for professional development. It is:
- Not accredited by a recognized body
- Not regulated by an authorized institution
- Complementary to formal qualifications
You'll receive a certificate of completion upon successfully finishing the course.
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