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Title
Text copied to clipboard!Director of Clinical Trials
Description
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We are looking for an experienced and dedicated Director of Clinical Trials to lead and develop our clinical research team. As the Director of Clinical Trials, you will have overall responsibility for planning, executing, and monitoring clinical studies in accordance with applicable regulations and company objectives. You will work closely with researchers, physicians, regulatory authorities, and other stakeholders to ensure that studies are conducted safely, ethically, and efficiently. The role also includes responsibility for budget, scheduling, and resource allocation, as well as continuous follow-up of project progress and reporting to management. You will develop and implement strategies to improve processes and ensure high quality in all aspects of clinical trials. Furthermore, you will be a key person in building and maintaining relationships with external partners, such as CROs, hospitals, and academic institutions. You are also expected to stay updated on new regulations, trends, and technologies in the field of clinical trials. To succeed in this role, you need solid experience in clinical research, strong leadership, and the ability to make strategic decisions. You should be communicative, solution-oriented, and have a strong interest in developing both people and processes. If you want to contribute to the development of future medicines and medical treatments, this is the role for you.
Responsibilities
Text copied to clipboard!- Lead and oversee clinical trial programs
- Develop and implement strategies for clinical studies
- Ensure compliance with regulatory requirements and ethical guidelines
- Manage project budgets, resources, and timelines
- Build and maintain relationships with internal and external stakeholders
- Report project status to management and authorities
- Train and support team members in clinical research
- Identify and manage project risks
- Follow up and evaluate study results
- Drive continuous improvement of processes and procedures
Requirements
Text copied to clipboard!- University degree in medicine, pharmacy, life sciences, or equivalent
- At least 7 years of experience in clinical research
- Proven leadership and project management experience
- Strong knowledge of GCP and regulatory requirements
- Experience with budget and resource planning
- Excellent communication and collaboration skills
- Ability to make strategic decisions
- Fluent in Swedish and English, both spoken and written
- Analytical and solution-oriented
- Experience working with CROs and external partners
Potential interview questions
Text copied to clipboard!- What experience do you have leading clinical trials?
- How do you ensure compliance with GCP and regulatory requirements?
- Can you provide examples of how you managed budgets and resources in previous projects?
- Describe a challenge you faced in clinical research and how you solved it.
- How do you work to develop and motivate your team?
- What strategies do you use to manage multiple parallel projects?
- How do you stay updated on new regulations and trends?
- What experience do you have collaborating with CROs and external partners?
- What do you consider most important for ensuring high quality in clinical studies?
- How do you report project status to management and authorities?
