Senior Medical Director, Scientific Affairs (Early Phase)

Job Purpose:

In this highly visible role, the Medical Director, Early Phase Medical Sciences Europe provides therapeutic leadership and serves as a Subject Matter Expert on medical and scientific matters with both internal and external teams. As a Medical Director, you will demonstrate entrepreneurial spirit and confidently engage with key contacts to maximize opportunities for Parexel, i.e. its Early Phase, globally. You will serve as a trusted partner to industry leaders in the identification of more effective therapies and ultimately make a difference in the lives of patients.

In detail you may:Evaluate the Early Clinical Development Plan (Phase 1) for new compound and provide scientific guidance for sponsors, especially biotech companies.Represent and promote Parexel’s services and experiences at client and sponsor meetings particularly focusing on feasibility and scientific input to support the acquisition of new business.Review viability of proposed studies and provide advice on improving suitability of design for effectiveness, efficiency and ease of conduct in all stages.Initiate and drive prospective review, development and implementation of novel techniques and new modalities.Participate in the Risk Identification and Mitigation Process according to applicable Guidelines, including EMEA/CHMP/SWP/294648/2007 Rev. 1Support relevant medical training of Parexel’s personnel, clients and contractors.Publish abstracts, manuscripts and books.Any other duties as assigned.QualificationsSkills:Excellent interpersonal skills with well-developed communication skills.Detail oriented, with the ability to work creatively and timely in a fast-paced environment.Motivational abilities to assist business development and operations groups to achieve objectives (i.e. meet quarterly sales targets).Good problem-solving skills.Self-motivation with a willingness to accept responsibility and challenges.Willingness to travel at least one week out of each month.Computer skills; ability to use MS Office, especially MS Excel.Language skills: fluent verbal and written English is mandatory.Knowledge:Profound knowledge of clinical pharmacology.Profound knowledge and practical experience of applicable international and local guidelines and regulations (e.g. EMA, FDA, GCP, ICH).Good knowledge and practical experience with clinical drug development and experimental designs.Experience:Relevant time of hospital training in Internal Medicine, Anesthesia, Neurology or Pediatrics.Experience in Clinical Pharmacology at a Medical School, in the Bio-Pharmaceutical Industry, CRO Industry or Healthcare Industry.Good understanding of Early Clinical Drug Development and Pharmacokinetics, with focus on First in Human Studies.Competent in relation to Medical Writing skills.Basic understanding of Biostatistics and Data Management.Education:Medical Doctor (MD, Physician)Valid license to practice medicine in a European countryProfound expertise in Pharmacology and PharmacokineticsWe offer:Use your clinical and research expertise to play a key role in bringing new treatment to the world.Leverage your clinical and research experience combined with consultative approach and communication skills in the industry.Flexibility to work from home while still having an impact on the lives of patients.High level of prognostics and impact.Strong opportunity for further career development as part of a succession plan.

“I found great flexibility in this job, which leads to better work life balance than in an academic setting. This really allows me to be more actively engaged when I am at work and more present at home. If you are looking for a Medical Director position that’s challenging, exciting and fun, then consider working at Parexel.” Heidi Cho – Medical Director at Parexel Americas