Drug Safety Specialist (m/f/d)

Rahmendaten

<p><strong>Framework:</strong></p> <ul> <li>Duration: 6 Monate  <li>Working Hours: 30- 40 h / Woche <li>Location: remote <li>Start Date: 01.12.2023 <li>latest start date: 01.01.2024 </ul> <br> <strong>Tasks</strong>:  <ul> <li>Evaluating the safety of investigational drugs in clinical trials, particularly combination therapies. <li>Generating safety reports and ensuring compliance with all regulatory requirements. <li>Collaborating with various departments to ensure accurate capture and reporting of safety data. <li>Experience in pharmacovigilance within Drug Safety. <li>Supporting in the execution of clinical marketing activities and experience in working with healthcare professionals. <li>Actively participating in ongoing clinical trials and reporting on combination therapy studies. </ul> <br> <strong>Requirements</strong>: <ul> <li>Medical degree or equivalent qualification. <li>Proven experience in Drug Safety, especially with combination therapies. <li>Strong knowledge of PV Drug Safety and experience in safety report generation. <li>Excellent English language skills, both written and spoken. <li>Experience in collaborating with various healthcare professionals. <li>Flexibility and willingness to work 30-40 hours per week. <li>Ideally, experience in collaborating on clinical marketing activities. </ul>