Director, Study ManagementLocation London, United Kingdom Apply
BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options.
BioMarin Global Medical Affairs (GMAF) offers scientific and clinical expertise to post-marketing products through the direction and planning of medical communications, support of education and research, liaising with the medical community, response to incoming inquiries about Medical Affairs products and trials, and leadership of the execution of Medical Affairs trials.
Within GMAF, the Study Management (SM) group is responsible for managing the strategy, execution, and analytics behind BioMarin’s studies, ensuring efficient, comprehensive, and compliant data collection to supportBioMarin products.
The Director is accountable for all GMAF SM activities across multiple products. The Director is responsible for developing the strategy for GMAF SM across their assigned products and is a key contributor to cross-functional strategy within GMAF SM. The Director is responsible for leading cross-functional initiatives, including departmental process improvements, and may act as an advocate for the group across the organization. Key areas of focus for the Director include people management, proactive risk and issue identification, development of mitigation strategies, cross-functional program team leadership, and successful trial execution within assigned products.
The individual in this position exhibits advanced skills in problem solving and decision making. S/he exhibits mastery of all other GMAF SM core and technical competencies.
Responsibilities may include, but are not limited to:
Contracts and Vendor Management
Trial Oversight and Communication
Data Quality and Compliance
People Management and Development
Strategic Leadership and Change Management
The Director is expected to exhibit mastery-level understanding of multiple core competencies, including leadership, strategic thinking, and people management. This includes (but is not limited to):
As a Director, mastery of drug development and therapeutic area knowledge are essential. This includes (but is not limited to):
BioMarin offers comprehensive career development programming, including guidance, targeted training opportunities, and mentorship programming. A career development pathway for GMAF has been defined and is available to employees of BioMarin.
The Director may manage up to 6 direct reports and multiple hierarchal levels of reports
EDUCATION AND EXPERIENCE
WORK ENVIRONMENT / PHYSICAL DEMANDS / TRAVEL
The employee may frequently be required to sit and talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities by this job include close vision, depth perception and ability to adjust focus.
Computer work utilizing common business software programs and hardware solutions.
Internal:Clinical Operations, Pipeline Commercialization, Market Access, Medical Communications, Regulatory Affairs, Patient Advocacy, Medical Directors and Medical Science Liaisons, Medical Information, Legal, Corporate Ethics & Compliance, Corporate Communications, Pharmacovigilance, Biometrics, Development Sciences Quality (DSQ), Business Operations
External:Clinical Trial Site Staff, vendors and suppliers