Global Clinical Director Freelance (m/w/d)

Rahmendaten

<u><strong>Rahmendaten</strong></u> <ul> <li>Laufzeit: 12-24 Monate</li> <li>Auslastung: 4-5 Tage/Woche (Vollzeit)</li> <li>Einsatzort: Norddeutschland</li> </ul> <br /> <u><strong>Your role:</strong></u> <ul> <li>Accountable for the clinical development strategy and alignment with multidisciplinary project team objectives, informing key stakeholders and gaining support</li> <li>Accountable for the design and delivery of clinical programs in accordance with international medical/scientific and quality standards and within timelines and budget</li> <li>Accountable for the safety monitoring, medical oversight, reporting (leading to registration) and publication of clinical trials (phase II-IV, post marketing support)</li> <li>Accountable for providing in-depth clinical knowledge of the 2 TAs under consideration</li> <li>Accountable for delivery of work of direct and indirect reportees within global and region</li> <li>Adequate people and stakeholder management, provides direction to achieve business objectives, efficiently delegate tasks and give clear guidance.</li> </ul> <br /> <u><strong>Your Profile:</strong></u> <ul> <li>Education: MD or PhD or MD/PhD</li> <li>At least 10-15 years of experience in pharmaceutical industry with minimum of 5- 8 years in relevant clinical development</li> <li>Ability to lead clinical programs and to run teams in multi-cultural environment at different sites</li> <li>Expert knowledge of clinical trial methodology, oversight/evaluation of safety and regulatory requirements governing clinical trials</li> <li>strong communication silks (written and oral) in English</li> </ul>