Maximizing site performance and site engagement in conducted clinical studies. Leveraging strong clinical operational and therapeutic expertise (scientific, clinical, disease states, and treatment alternatives knowledge within the therapeutic area(s)) to support execution of the clinical studies.

Responsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory requirements.  Engages with clinical sites to develop, build, and maintain strong relationships with investigators/staff that will ensure high quality investigative sites to support clinical development programs. Collaborate with internal and external stakeholders as well as third party vendors. Provide operational support to the CPM/Sr CPM to deliver the study within planned timelines and according to required standards of quality and compliance. Evaluate, screen and develop high quality investigative sites to support clinical development programs.

• Develop, communicate, and execute Site Engagement Strategy/Plan working closely with the Clinical Team and key internal stake holders throughout the life cycle of clinical trials.
• Support clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of trials.
• Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication channels to create awareness of and its activities thereby increasing their desire to partner with sponsor. 
• Develop & maintain relationships with site engagement organizations; assist in identification of high performing sites and key opinion leaders that can contribute to forums, boards and/or discussions.
• Interact/train new investigators to work on clinical trials.

• Strong facilitation skills
• Good collaborator
• Clear and articulate verbal, written and presentation skills with excellent command of English and/or other language
• Excellent verbal and written communication
• Ability to operate effectively within an international and rapidly changing environment

• Ability to supervise monitoring and related activities in a clinical trial.
• Ability to work without close supervision; ability to work under stress and within a team environment.
• Proficient in MS Office Suite.
• Curious and agile, “nothing is impossible” mentality.
• Ability to have scientific discussions with Investigators and Site Personnel
• Able to problem solve
• Ability to analyze, synthesize, and clearly present information to individuals and groups
• Ability to travel at least 50% of the time (including overnight stays, possible global).