Trial leader, clinical

What does a clinical trial supervisor do? – Tasks and work environment

A clinical trial supervisor is responsible for planning, leading, and monitoring medical studies on humans. Tasks include designing research protocols, ensuring studies follow ethical guidelines, supervising research teams, and reporting results to authorities and pharmaceutical companies. The role also involves close contact with research participants, healthcare personnel, and regulatory agencies. The work is usually conducted in a laboratory environment or on clinical research units, where high standards for accuracy and documentation are required. The pace can be intense, especially during project-heavy periods, and the work environment is characterized by collaboration across different professions.

Salary development over time

The salary for clinical trial supervisors has shown strong growth in recent years. In 2022, the average salary was 59,400 SEK per month, followed by a temporary decline to 56 100 SEK in 2023. In 2024, however, the salary increased significantly to 65 600 SEK, corresponding to an increase of about 17% compared to the previous year. This salary increase can partly be explained by an increased demand for qualified personnel in clinical research, as well as a generally higher educational level among those recruited to the profession. Fluctuations between years also reflect economic conditions and industry-specific factors, such as research funding and ongoing clinical trials. Today, the salary level is clearly above the average for similar professions.

Clinical trial supervisor salary – comprehensive overview

• Average salary: 65 600 SEK/month
• Lowest salary: 40,500 SEK/month (women), 42,800 SEK/month (men)
• Highest salary: 67,600 SEK/month (women), 76,400 SEK/month (men)
• Hourly wage (average): 395 SEK
• Gender differences: Women earn 88% of what men do (63 600 SEK/month compared to 72 200 SEK/month)
• Regional differences: Data on regional differences is not available

Education and qualifications

To work as a clinical trial supervisor, a solid educational background in medicine, pharmacology, or biomedicine at an advanced level is required. Experience in clinical research and good knowledge of regulatory requirements within drug testing are often sought after. Employers prefer candidates with international experience or participation in larger research projects. GCP (Good Clinical Practice) certification is advantageous.

• Formal degree: Master's in biomedicine, pharmacy, or medicine (5 years)
• Certification: GCP (Good Clinical Practice)
• Internship: Clinical practice or research projects during education
• Prerequisites: Science-based upper secondary education
• Tips: Engagement in research projects and networking within the industry

Common benefits and compensations

Common benefits for clinical trial supervisors include occupational pension, wellness allowance, flexible working hours, and remote work options. Additional perks may include skills development, conference travel, and participation in international projects. Some employers also offer bonus programs linked to project results.

Competition and challenges

The competition for positions as a clinical trial supervisor is generally high, especially in metropolitan areas and research-intensive environments. Challenges in the profession include managing complex projects with high regulatory demands and strict deadlines. Ensuring patient safety and data quality is crucial and requires continuous updating of knowledge in legislation and research methodology. Staying current with international guidelines and being able to adapt quickly to changing conditions are prerequisites for success. Additionally, funding and access to research resources can impact workload and job security.

Tips for those who want to become a clinical trial supervisor

To succeed as a clinical trial supervisor, it is beneficial to combine analytical skills with great attention to detail, as the work involves handling complex data and strict documentation. Good collaboration skills facilitate teamwork across disciplines, while communication skills are essential for conveying study results and handling contacts with authorities. Flexibility and resilience under pressure are important, especially when project plans need quick adjustments. Having a genuine interest in research and medical development is also advantageous, as it motivates long and sometimes challenging studies. Building a network within the industry and seeking internships early can help gain experience and contacts.

Key facts about clinical trial supervisors

• Educational level: Master's degree in biomedicine, pharmacy, or medicine
• Work environment: Laboratories, research clinics, and office settings
• Demand: 143 job openings in the field right now
• Typical employment type: Project-based or permanent positions at pharmaceutical companies or universities
• Special skills: GCP certification, regulatory expertise, and experience in clinical research

Career paths and future prospects

After three to five years as a clinical trial supervisor, opportunities may open for advancement to senior roles such as project manager for clinical trials or head of research and development departments. Other career options include regulatory specialist roles, work within health authorities, or international research organizations. The job market outlook is difficult to assess as the profession is part of a larger occupational group, but the number of available positions suggests a stable or increasing demand. The Employment Service does not make a separate assessment for clinical trial supervisors, but there is generally good demand for qualified pharmacologists and biomedical scientists, especially in connection with increased investment in clinical research and drug development.

Frequently asked questions about clinical trial supervisors

• What does a clinical trial supervisor earn?
  - The average salary is 65 600 SEK per month, but it can vary depending on experience and employer.
• What education is required to become a clinical trial supervisor?
  - A master's degree in biomedicine, pharmacy, or medicine, along with GCP certification, is recommended.
• What are the gender differences in salary?
  - Women earn on average 88% of what men do in the profession.
• What workplaces are common for clinical trial supervisors?
  - Pharmaceutical companies, universities, research clinics, and authorities are common employers.
• Are there many job openings for clinical trial supervisors?
  - There are currently 143 job openings in the pharmacology and biomedical fields.
• What is the highest and lowest salary?
  - The highest salary is 76,400 SEK (men), and the lowest is 40,500 SEK (women).
• Is experience necessary to get a job as a clinical trial supervisor?
  - Yes, experience in clinical research and project management is often required.