Senior Clinical Research Associate
Atos Medical
- Malmö
- Permanent
- Heltid
- Independently develop clinical investigation documents, such protocols, case report forms, and patient information for clinical studies.
- Manage and coordinate ethical and competent authority submissions and approvals.
- Communication with investigators and internal stakeholders
- Monitor clinical studies to ensure adherence to protocols and patient safety, primarily in-house
- Analyze study data and compile comprehensive reports on study outcomes.
- Collaborate closely with commercial teams to integrate study findings into promotional materials
- Assess and validate the quality and accuracy of marketing and market access materials content based on available clinical studies and publications.
- Provide support to junior team members and students
- PhD or master's degree in Life Science, Natural Science, or Medicine.
- Minimum of 3 years' experience in clinical studies, preferably within the MedTech industry, and working in accordance with ISO-14155 and MRD
- Experience with ethical and competent authority submissions
- Proficiency in English and familiarity with Microsoft Office suite.
- Experience with study management tools such as eTMFs and EDCs is highly desirable.
#LI-AT