When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Do you want to make an impact in your next role? Parexel is looking for changemakers who are driven by curiosity, passion, and optimism. Come join us in keeping the Patient at the Heart of Everything We do. Parexel has new opportunities for home-based Study Start Up Leaders to join our global team. Global experience is preferred, but not required. The Study Start-Up Leader is accountable for the execution of the study start-up strategy and planning, including the management and coordination of start-up activities such as alignment to country regulations, Core/Site document collection/ approval, ICF customization/approval, EC and RA/ MoH submissions, SIV scheduling and activation requirements. The Senior Study Start-Up Leader, is accountable as noted above including: • Acting as study-level program lead, such as managing multiple protocol delivery for a Sponsor or asset development. • Acting as an Enterprise or Biotech level lead and provide expert level knowledge on agreed partnership process. • Additional responsibilities may include: Study Start-Up Leader mentorship Participation in training and support programs Fulfilling subject matter expert or process improvement roles with Clinical Operations Key Accountabilities: • Manage the study start up process, through development of a site activation strategy and to oversee start-up delivery and governance. • Coordinate, develop and articulate the critical path planning, and implement as part of the Site Initiation Scheduling, System Set-up, EDL Management, EC & RA/ MoH Strategy, ICF Customization, Risk Mitigations, Monitoring Plan, Site Activation Requirements & Relevant Tools. • Collaborate and communicate within the Global study team matrix to provide study start up strategy, input to milestone development, and alignment of operational targets to ensure timely delivery of study start up activities. • Participate in client meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics. • Partner closely with both Functional Leaders and Local Site Managers to proactively identify study start up related issues • Develop and execute corrective actions to mitigate risks to activation timelines • Ensure that relevant - systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level). • Deliver and maintain client-focused reporting to measure performance and proactively identify issues for resolution. • Ability to travel, as required. Knowledge and experience: • Proven client-facing relevant experience in healthcare, clinical research, project management or contract research organization • Global experience in SSU is preferred but not required • 2 years' experience working as a Study Start Up Leader (SSUL within a CRO, Biotech or Pharma preferred; additional years of experience required at the Senior level • Minimum 2 years of experience in project scheduling, managing resources, budgets and coordinating team activities • Must be detail-oriented; proficient in Windows environment and possess superior interpersonal skills and organizational skills • Competent in written and oral English Education: • Undergraduate degree preferably in a clinical or health related field required • Advanced degree preferred Parexel Benefits: Health, Vision & Dental Insurance Tuition Reimbursement Vacation/Holiday/Sick Time Flexible Spending & Health Savings Accounts Work/Life Balance 401(k) with Company match Pet Insurance Full list of benefits available here: US Benefits | Parexel International At Parexel we embrace flexibility and understand that in today’s fast-paced world, employees need to balance their careers with their personal lives. Come join us where learning is constant, you’re exposed to a world of experiences and open doors. EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.