Director, Site Intelligence and Activation (Line Management)
Experience and Education Requirements:
Bachelor’s degree or higher in a scientific or related discipline
Demonstrates depth of knowledge/ experience of clinical drug development and trial process, attained within the pharmaceutical industry and/or CRO
Significant evidence of successfully leading operations within a regional/global complex matrix environment
Project management/product development experience
Valid Passport
Or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities.
Required Knowledge, Skills and Abilities:
Demonstrated strategic thinking, planning and organization skills.
Ability to analyze data, anticipate and mitigate risk, exercise sound judgment, problem solving and decision-making working under pressure and at times with limited desired information.
Uses personal influence and persuasion to effectively promote ideas and proposals to shape stakeholder opinions
Demonstrates the ability to develop and cultivate strong internal/external networks of contacts and resources to help ensure operational execution
A relationship builder who is able to work effectively in matrix environments
Is an ambassador for change, influences and motivates, demonstrates solid interpersonal and conflict resolution skills
Effective negotiation and problem solving skills
Demonstrates credible leadership style, with concise, well organized oral and written communication skills and proven ability to mobilize and foster team productivity.
Ability to motivate managers and supervisors to define and reach team objectives
Expertise in budgeting, forecasting, and resource management
Effective oral and written communication skills including the ability to communicate in English, both orally and in writing
Must be extremely efficient, well organized and demonstrate a strong attention to detail
Computer skills, particularly word processing and spreadsheets (MS Word and MS Excel)
Must be able to work independent of direct supervision
Has a solid understanding of FDA, GCP, and ICH guidelines with a track record of successful operational delivery