University / college degree, certification in a related allied health profession from an appropriately accredited institution, or relevant experience.
Mush have broad knowledge of drug development processes with particular expertise in clinical trial data handling practices and relevant regulations.
Expertise in resource management within a CRO setting.
Thorough knowledge of time and cost estimate development and CRO service pricing strategies.
Minimum seven years of relevant work experience with four or more years supervisory experience to include data management, clinical operations, biostatistics or related field and experience to include data management, clinical operations, biostatistics or related field and knowledge of several therapeutic areas.
Demonstrated skill for management of staff exceeding 10 employees across one or more locations within a region.
Excellent oral and written communication and presentation skills.
In depth knowledge of clinical trial processes and data management, clinical operations, biometrics, and systems applications to support operations.
Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
Operational experience in other disciplines such as clinical, biometrics, medical writing, pharmacovigilance, safety, quality assurance, regulatory, etc.
Demonstrates ability to lead change by example and achieve results.
Demonstrate ability to handle multiple competing priorities simultaneously across and assortment of projects and initiatives.
Demonstrated ability to inspire effective teamwork and motivate staff.
Proven managerial and interpersonal skills.