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Title
Text copied to clipboard!Clinical Trials Director 2
Description
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We are looking for an experienced and motivated Clinical Trials Director 2 to join our team. In this role, you will be responsible for the planning, coordination, and execution of clinical trials, ensuring compliance with regulatory requirements and company quality standards. You will play a key role in all phases of the research process, including protocol development, site selection, investigator training, patient recruitment oversight, and coordination of data collection and analysis.
Success in this position requires a strong understanding of clinical trials, Good Clinical Practice (GCP) guidelines, and the medical research environment. You must have excellent communication and organizational skills, as well as the ability to lead cross-functional teams and projects in an international setting. Additionally, we expect the ability to analyze research data and clearly report findings to various stakeholders.
As a Clinical Trials Director 2, you will collaborate with medical, regulatory, quality assurance, and marketing teams to ensure smooth trial progress and effective use of results in product development. This role offers the opportunity to directly impact the development of new drugs and therapies and improve patient safety.
We offer a competitive salary, flexible working hours, remote work opportunities, and the chance to grow your career as part of an innovative and international organization.
Responsibilities
Text copied to clipboard!- Plan and coordinate clinical trials
- Develop and approve study protocols
- Select research sites and investigators
- Oversee and support patient recruitment
- Ensure data collection and quality
- Collaborate with regulatory and quality teams
- Manage clinical trial budgets
- Prepare study reports and present findings
- Organize training for research staff
- Support audits and inspections
Requirements
Text copied to clipboard!- Relevant university degree (e.g., biomedical sciences, pharmacy, medicine)
- At least 5 years of experience in clinical trials
- Strong knowledge of GCP and regulatory requirements
- Excellent project management and organizational skills
- Ability to work in international and cross-functional teams
- Strong communication and negotiation skills
- Experience managing research budgets
- Fluency in Finnish and English
- Ability to analyze and report research data
- Willingness to travel as needed
Potential interview questions
Text copied to clipboard!- Describe your experience managing clinical trials.
- How do you ensure compliance with GCP guidelines?
- What challenges have you faced in research projects and how did you solve them?
- Describe your experience with managing research budgets.
- How do you effectively lead a cross-functional team?
- How do you ensure successful patient recruitment?
- Give an example of a successful research project.
- How do you handle data quality and integrity?
- How do you work with regulatory authorities?
- What motivates you to work in clinical research?
