BASIC QUALIFICATIONS

• MD or MD/PhD with minimum of 1 year of clinical experience or experience in drug development
• Understanding of clinical trials methodology
• Collaboration skills
• Excellent verbal and written communication skills in English
• Ability to travel nationally and internationally

PREFERRED QUALIFICATIONS

• Pulmonary medicine, Immunology, Rheumatology, Allergy, or Dermatology background is desirable.
• Experience in the design, execution and interpretation of Late Stage clinical trials

• Provide medical and scientific leadership in the global development of new medicines targeted at indications in the field of respiratory diseases and wider range of immunological disorders
• Provide medical and scientific leadership in the innovative design, execution and interpretation of clinical trials in one or more development programs.
• Build strong relationships with a network of external scientific experts.
• Work closely with colleagues in other functions including Patient Safety, Regulatory Affairs, and Clinical Operations.
• You will be involved primarily in late stage (Ph2b and later) clinical programs but will collaborate with colleagues supporting Early (R&I) stage programs as well as medical affairs colleagues.
• Lead and contribute to medical monitoring of trials
• Provide expert medical input into the preparation of regulatory documents and interactions with regulatory authorities.
• Provide expert medical and scientific analysis and interpretation of data from ongoing studies and in the literature.
• Develop and review protocols, informed consent, investigator’s brochure and other clinical development documents.
• Participate in the preparation of scientific publications and presentations at scientific meetings and congresses.