Beschreibung
Medical Director - Clinical Development (m/f/d)
Reference: -en
Start: asap
Duration: 12 MM++
Main tasks:
- Stays abreast of internal and external developments, trends and other dynamics relevant to the work of CD to maintain, at all times, a fully current view and perspective of influences and/or implications for the assigned therapeutic and disease area(s)
- As appropriate, participates in competitive intelligence and/or other market/industry assessment activities and projects
- Maintains the highest standards and levels of scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment
- Collaborates with a variety of internal and external partners and stakeholders, such as clinical investigators, clinicians, scientists and key opinion leaders (KOLs), as well as multidisciplinary internal groups, including other groups in PD, research, regulatory, business development, commercial operations, legal, etc.
- Participates in CD strategy development
- As assigned, may also consult to pharma partnering on relevant acquisitions, joint ventures or other strategic partnerships, as these potentially relate to the assigned therapeutic/disease area(s)
- Participates in development of the CD plan for assigned molecule(s)/indication(s) and/or other programs
- Supports other CST members in preparing for HA meetings. As appropriate, participates in HA meetings. Ethically, effectively and professionally represents the interests of Roche and patients
- Designs and develops clinical studies for review and discussion with other CST members
- May collaborate with others in the development of the product safety profile
- Collaborates with others in development of clinical sections of investigator brochures, presentations and other materials
- May participate in the identification and selection of appropriate external investigators and sites
- Collaborates with others in development of study analytics and data management plans
- Participates in investigator and other external presentations, meetings and other communications
- May act as a medical monitor for assigned studies
- Conducts ongoing reviews of medical/safety data
Main qualifications
- M.D. with relevant medical experience in psychiatry (PTSD, anxiety disorders, schizophrenia)
- Working knowledge of the US healthcare System is an asset
- Some years professional experience and understanding of Phase II – III drug development
- Professional experience in working with the principles and techniques of data analysis, interpretation and clinical relevance (e.g. ISS, ISE, competitor data, etc.)
- Professional experience developing product and safety profiles
- Has working knowledge of the multi-disciplinary functions involved in a company’s drug development process, e.g. clinical operations, biostatistics, regulatory, commercial operations, etc.
- Excellent project management skills: can prioritize multiple tasks and goals and ensure the timely, on-target and within budget accomplishment of such
- Good interpersonal, verbal communication and influencing skills; can influence without authority
- Strong written communication skills
Main advantages:
- You will work in an international environment
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
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My contact person:
Emina Mustafic
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