Responsibilities:
Develop clinical operational strategy and ensure clinical research programs are executed with quality and efficiency, on-time, within budget, and to meet company objectives.
Translate asset strategy into operational execution by developing the clinical operations plan (or strategy) and connecting the science with the business, operations, and patients.
Identify and evaluate risks and mitigations at program level to achieving the asset strategy.
Interacts with and influences all levels of management and cross-functional team members to achieve program objectives and represents Clinical Operations at senior leader cross functional meetings.
Reviews and provides clinical operations content to clinical and regulatory documents.
Manage overall budget management across multiple studies.
Responsible for bringing the best out of our talent, mentoring and supporting development to enable growth including direct management of study manager(s).
Create an inclusive, innovative and learning environment where staff and studies/programs will succeed.
Execute clinical programs in compliance with quality standards (ICH/GCP, Global Regulations, and corporate policies and procedures).
Strong communication and stakeholder management skills. Is comfortable with not having all the information yet able to drive activities and find solutions to deliver on the program.

Qualifications
Master’s degree or equivalent is required, typically in nursing or scientific field. An equivalent with relevant industry experience is acceptable.
5+ years of Pharma-related/ clinical research related experience (and/or applicable work experience) , including approximately 2 years from multinational corporation (MNC).
8 years (and/or applicable work experience) in clinical research demonstrating a high level of core, technical and leadership competencies through setting and driving strategy.