OTHER SKILLS AND ABILITIES: Strong leadership and organizational management skills in planning, strategizing, managing, monitoring, scheduling, and critiquing Ability to exercise sound judgment and make decisions independently and to proactively identify and solve problems Ability to provide experience and input into initiatives relating to interacting with sites and/or customers Ability to motivate, lead and engage a team Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment Strong oral and written communication skills to clearly and concisely present information Demonstrated ability to collaborate across the business Team-oriented work style; seeks and gives guidance Understanding of regulatory processes and guidelines Understanding of initiation, planning, and execution of clinical projects and overall project planning Awareness of ICH GCP Guidelines and the FDA/EU Clinical Trials Directives/National regulations (CTAs, Amendments, Urgent Safety Measures, End of Trial Notifications) Ability to handle multiple tasks in a fast-paced and constantly changing environment Ability to work in an organized, methodical, and self-motivated manner Proficiency in MS-Office applications including Microsoft Word, Excel, and PowerPoint; digital systems aptitude REQUIREMENTS: * A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or other related science OR two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and experience within clinical research (e.g. Ensure OOS activities are tracked and captured within Change Notification Form (CNF) and follow through to execution of change order Work in conjunction with assigned project team members to develop and maintain site activation related project plans May contribute to the development, review, and maintenance of SOPs and best practice guidelines and provide training/coaching pertaining to activities of the Site Activation department Provide input to departmental process improvement initiatives Establish and interpret site activation metrics to help drive corrective action for achieving deliverables, milestones and/or KPIs May participate in business development activities by contributing to proposals and bid defense meetings by preparing relevant sections of proposals, budgets and other country and/or study specific activities related to Site Activation Report and/or escalate issues to Line Manager, Site Activation Portfolio Lead and/or Site Activation Therapeutic Lead to ensure resolution and minimize risks to on-time deliverables Comply with SOPs, ICH GCP and national regulations as applicable Liaise with other functional contributors and vendors as needed Perform other duties as assigned The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.