Associate Director Clinical Development, Respiratory

Proclinical is working with a world leading biotechnology company that is seeking an Associate Director of Clinical Development to be based in Cambridge, Uk on a permanent basis.

Job Responsibilities:

• Key role in design, implementation and execution of clinical studies:
• Establish and approve scientific methods for design and implementation of clinical study protocols (CSP), data collection systems and final reports.
• Ability to analyse, synthesize and interpret clinical data in both ongoing and completed studies for safety surveillance (acting as medical monitor where applicable) and publications.
• Identify, select and train clinical research centres and investigators.
• Overseas planning and management of investigator meetings, advisory boards and other scientific committees as required by the CSP (e.g. independent reviews, DSMBs etc.).
• Collaboration with project team members in all elements of clinical studies including regulatory, translational and research colleagues
• Work with R&D and other senior management in assessing requirements for emerging products, including next generation candidates
• Commercial to design research to have maximum marketplace credibility and enhance
• marketing efforts.
• Both internal and external (oral and written communication) on clinical development plans, clinical study designs and results.
• Contribute to key department and company initiatives as applicable to role, skills and experience.

Skills and Requirements:

• PhD (preferably respiratory or allergy) with industry experience or M.D. degree or equivalent, ideally board certified (or eligible) preferred in pulmonary medicine or allergy.
• Clinical study conduct in a pharmaceutical, CRO or healthcare environment.
• Must be an excellent communicator with proven leadership skills and the ability to interact collaboratively in a cross functional environment.
• Must integrate and analyse non-clinical and clinical data as well as data/input from multiple internal and external functional areas. Synthesis of previous clinical data and ongoing deadlines/priorities.
• Role is that of individual contributor. Must be able to operate independently in medical, safety and clinical development tasks with minimal supervision. Once direction is provided, must identify problems, generate solutions (or options) and follow agreed plans through to conclusion.

To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Tom Russell on +44 203 8246 104 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

#LI-TR1